23 results on '"Lenin Domínguez-Ramírez"'
Search Results
2. Molecular Characterization of a Functional Membrane-Associated Progesterone Receptor Component 2 (PGRMC-2) in Maturing Oocytes of the Human Parasite Nematode Trichinella spiralis: Implications to the Host-Parasite Relationship
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Alejandro Sánchez-González, Martín García-Varela, Jorge Morales-Montor, Karen Elizabeth Nava-Castro, Romel Hernández-Bello, Víctor Hugo Del Río-Araiza, Álvaro Colin-Oviedo, Lenin Domínguez-Ramírez, José Prisco Palma-Nicolás, and Gloria María. González-González
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Nematode ,Membrane associated ,biology ,Human parasite ,Progesterone receptor ,Trichinella spiralis ,Helminths ,biochemistry ,biology.organism_classification ,Cell biology - Abstract
We explored the hypothesis that progesterone direct effect on Trichinella spiralis might be mediated indeed by a new steroid-binding parasite protein. Our first results showed that Progesterone decreases the parasite molting rate. We amplify, isolated, cloned and sequenced the PGRMC2 sequence using specific primers from known species. Furthermore, we expressed the protein and developed an antibody to performance immunofluorescent confocal microscopy, where detected that parasite cells showed expression of a P4-binding protein exclusively located at the oocyte and the parasite´s cuticle. Presence of the PGRMC2 protein in these cells was also confirmed by western blot and flow cytometry. Molecular modeling studies accompanied by computer docking using the sequenced protein showed that PGRMC2 is potentially able to bind steroid hormones such as progesterone, estradiol, testosterone, and dihydrodrotestosterone with different affinities. Phylogenetic analysis and sequence alignment clearly demonstrated that Trichinella spiralis PGRMC2 is related to a steroid-binding protein of another platyhelminths. Progesterone may probably act upon Trichinella spiralis oocytes probably by binding to PGRMC2. This research has implications in the field of host-parasite co-evolution as well as the sex-associated susceptibility to this infection. In a more practical matter, present results may contribute to the molecular design of new drugs with anti-parasite actions.
- Published
- 2021
3. Molecular dynamic simulations of the catalytic subunit of calpains 1, 2, 5, and 10: Structural analysis with an aim toward drug design
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Raúl Pérez-Estrada, Antonio Romo-Mancillas, Lenin Domínguez-Ramírez, Roselyn Lemus, and Francisco Kuribreña-Romero de Terreros
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Drug ,Proteases ,media_common.quotation_subject ,Protein subunit ,Computational biology ,Molecular Dynamics Simulation ,01 natural sciences ,Biochemistry ,Molecular dynamics ,Catalytic Domain ,Drug Discovery ,Humans ,Homology modeling ,media_common ,Glycoproteins ,Pharmacology ,Binding Sites ,biology ,010405 organic chemistry ,Chemistry ,Calpain ,Organic Chemistry ,0104 chemical sciences ,Isoenzymes ,Molecular Docking Simulation ,010404 medicinal & biomolecular chemistry ,Docking (molecular) ,Drug Design ,biology.protein ,Molecular Medicine ,Cysteine - Abstract
Calpains are cysteine proteases involved in the development of several human chronic illnesses such as neurodegenerative diseases, cardiovascular ailments, diabetes, and obesity which constitutes them into possible therapeutic targets. Here, using molecular dynamic simulations and docking, we studied the binding of known inhibitors to representative members of classical and nonclassical calpains. Our aim is to gain better understanding on the inhibition mechanism of calpains and to develop better and more specific inhibitors. Our atomistic models confirmed the importance of calcium ions for the structure of calpains and, as a consequence, their functionality. With these models and their subsequent use in molecular docking, essential structural requirements were identified for the binding of ligands to the calpain catalytic site that provide useful information for the design of new selective calpain inhibitors.
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- 2018
4. In Silico Mutagenesis, Docking, and Molecular Dynamics: Their Role in Biosensor Design for Environmental Analysis and Monitoring
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Paulina Cortés-Hernández and Lenin Domínguez-Ramírez
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Molecular dynamics ,Biochemistry ,Environmental analysis ,Chemistry ,Docking (molecular) ,In silico mutagenesis ,Protein design ,food and beverages ,Binding site ,Biosensor ,Molecular biology ,Protein concentration - Abstract
Biosensor design is an active area of research that spans several disciplines and techniques ranging from biotechnology to nanotechnology. In the former, it is often the case that de novo design is shunned in favor of redesigning an existing protein. In the present chapter, we will focus on the latter strategy and emphasize its application on a protein from cow milk, β-lactoglobulin (BLG). BLG is a protein component of ungulates’ milk. It is present in cow, goat, and sheep; their milk is widely consumed by humans. Human milk lacks this protein entirely. It is a small protein made up by β-sheets and containing, at least, two disulfide bridges. It can form homodimers; it can monomerize or oligomerize depending on conditions such as pH, protein concentration, and others. Its binding site is unique due to its hydrophobicity. As far as structural information shows, this binding site is a cavity that is exposed to the solvent but not occupied by it. Considering this information, it should be no surprise that BLG binds fatty acids and liposoluble vitamins. While BLG’s biological function is unknown, its hydrophobic binding site can potentially bind other hydrophobic compounds such as medicines, pesticides, or even persistent organic pollutants. Thus, understanding of the physicochemical properties of BLG, its binding site, and its engineering and redesign could lead to biosensors to monitor hydrophobic pollutants.
- Published
- 2017
5. Role of cis-trans proline isomerization in the function of pathogenic enterobacterial Periplasmic Binding Proteins
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Lenin Domínguez-Ramírez and Paulina Cortés-Hernández
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0301 basic medicine ,Conformational change ,Isomerization ,Proline ,Stereochemistry ,Bioinformatics ,lcsh:Medicine ,ATP-binding cassette transporter ,Molecular Dynamics ,Research and Analysis Methods ,Molecular mechanics ,Biochemistry ,Microbiology ,Isomers ,03 medical and health sciences ,Database and Informatics Methods ,Computational Chemistry ,Isomerism ,Enterobacteriaceae ,Biochemical Simulations ,Binding site ,Amino Acids ,lcsh:Science ,Multidisciplinary ,Chemistry ,Organic Compounds ,Simulation and Modeling ,Organic Chemistry ,lcsh:R ,Chemical Reactions ,Chemical Compounds ,Biology and Life Sciences ,Proteins ,Computational Biology ,Cyclic Amino Acids ,Ligand (biochemistry) ,030104 developmental biology ,Periplasmic Binding Proteins ,Physical Sciences ,Periplasm ,lcsh:Q ,Sequence Analysis ,Sequence Alignment ,Research Article - Abstract
Periplasmic Binding Proteins (PBPs) trap nutrients for their internalization into bacteria by ABC transporters. Ligand binding triggers PBP closure by bringing its two domains together like a Venus flytrap. The atomic determinants that control PBP opening and closure for nutrient capture and release are not known, although it is proposed that opening and ligand release occur while in contact with the ABC transporter for concurrent substrate translocation. In this paper we evaluated the effect of the isomerization of a conserved proline, located near the binding site, on the propensity of PBPs to open and close. ArgT/LAO from Salmonella typhimurium and HisJ from Escherichia coli were studied through molecular mechanics at two different temperatures: 300 and 323 K. Eight microseconds were simulated per protein to analyze protein opening and closure in the absence of the ABC transporter. We show that when the studied proline is in trans, closed empty LAO and HisJ can open. In contrast, with the proline in cis, opening transitions were much less frequent and characterized by smaller changes. The proline in trans also renders the open trap prone to close over a ligand. Our data suggest that the isomerization of this conserved proline modulates the PBP mechanism: the proline in trans allows the exploration of conformational space to produce trap opening and closure, while in cis it restricts PBP movement and could limit ligand release until in productive contact with the ABC transporter. This is the first time that a proline isomerization has been related to the control of a large conformational change like the PBP flytrap mechanism.
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- 2017
6. Effects of a Buried Cysteine-To-Serine Mutation on Yeast Triosephosphate Isomerase Structure and Stability
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Adela Rodríguez-Romero, César A. Reyes-López, Lenin Domínguez-Ramírez, Edith González-Mondragón, Andrés Hernández-Arana, and Alejandra Hernández-Santoyo
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Models, Molecular ,crystal structure ,Protein Conformation ,molecular dynamics ,Saccharomyces cerevisiae ,stability ,triosephosphate isomerase ,Mutant ,Molecular Dynamics Simulation ,Crystallography, X-Ray ,Article ,Catalysis ,Triosephosphate isomerase ,lcsh:Chemistry ,Inorganic Chemistry ,Serine ,Protein structure ,TIM barrel ,Cysteine ,Physical and Theoretical Chemistry ,lcsh:QH301-705.5 ,Molecular Biology ,Spectroscopy ,Binding Sites ,biology ,Chemistry ,Organic Chemistry ,Wild type ,General Medicine ,biology.organism_classification ,Computer Science Applications ,Kinetics ,lcsh:Biology (General) ,lcsh:QD1-999 ,Biochemistry ,Mutation ,Triose-Phosphate Isomerase - Abstract
All the members of the triosephosphate isomerase (TIM) family possess a cystein residue (Cys126) located near the catalytically essential Glu165. The evolutionarily conserved Cys126, however, does not seem to play a significant role in the catalytic activity. On the other hand, substitution of this residue by other amino acid residues destabilizes the dimeric enzyme, especially when Cys is replaced by Ser. In trying to assess the origin of this destabilization we have determined the crystal structure of Saccharomyces cerevisiae TIM (ScTIM) at 1.86 Å resolution in the presence of PGA, which is only bound to one subunit. Comparisons of the wild type and mutant structures reveal that a change in the orientation of the Ser hydroxyl group, with respect to the Cys sulfhydryl group, leads to penetration of water molecules and apparent destabilization of residues 132–138. The latter results were confirmed by means of Molecular Dynamics, which showed that this region, in the mutated enzyme, collapses at about 70 ns.
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- 2012
7. The linker sequence, joining the DNA-binding domain of the homologous transcription factors, Mlc and NagC, to the rest of the protein, determines the specificity of their DNA target recognition inEscherichia coli
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Dominique Bréchemier-Baey, Lenin Domínguez-Ramírez, and Jacqueline Plumbridge
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Genetics ,chemistry.chemical_classification ,DNA-binding domain ,Biology ,medicine.disease_cause ,Microbiology ,Amino acid ,chemistry.chemical_compound ,chemistry ,Biochemistry ,Transcriptional regulation ,medicine ,Binding site ,Molecular Biology ,Linker ,Transcription factor ,Escherichia coli ,DNA - Abstract
Summary Protein–DNA recognition is fundamental to transcriptional regulation. Transcription factors must be capable of locating their specific sites situated throughout the genome and distinguishing them from related sites. Mlc and NagC control uptake and use of the sugars, glucose and N-acetylglucosamine. Both their helix–turn–helix motifs and their consensus binding sites on DNA are very similar. One distinguishing feature is that most NagC sites have a C/G bp at positions −11 and +11 from the centre of symmetry of the operator, while all Mlc sites have A/T. By constructing Mlc and NagC chimeras, we show that the helix–turn–helix motif per se is not responsible for specific recognition of Mlc or NagC sites, but that a linker, joining the DNA-binding domain to the rest of the protein, is the major determinant. We show that a change of just two amino acids in the NagC linker is sufficient to allow NagC to recognize an A/T bp at positions +/−11 and repress Mlc targets. Modelling of the NagC linker suggests that it forms an extended structure containing two arginines and we suggest that these arginines interact differently with the minor groove at positions +/−11 depending upon the presence of a C/G or A/T bp.
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- 2012
8. Role of Lysine ε-Amino Groups of β-Lactoglobulin on Its Activating Effect of Kluyveromyces lactis β-Galactosidase
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Lorena Gómez-Ruiz, Alma E. Cruz-Guerrero, Gabriela M. Rodríguez-Serrano, Lenin Domínguez-Ramírez, Judith Jiménez-Guzmán, Elizabeth Del Moral-Ramírez, and Mariano García-Garibay
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Models, Molecular ,Kluyveromyces lactis ,Binding Sites ,biology ,Lysine ,Succinic anhydride ,food and beverages ,Lactoglobulins ,General Chemistry ,beta-Galactosidase ,biology.organism_classification ,Enzyme Activation ,Kluyveromyces ,Succinylation ,chemistry.chemical_compound ,Enzyme activator ,chemistry ,Affinity chromatography ,Biochemistry ,biology.protein ,Thermodynamics ,Beta-galactosidase ,General Agricultural and Biological Sciences - Abstract
Native beta-lactoglobulin binds and increases the activity of Kluyveromyces lactis beta-galactosidase. Construction of a three-dimensional (3D) model of beta-lactoglobulin showed that lysine residues 15, 47, 69, and 138 are the most exposed ones, thus the ones more likely to interact with beta-galactosidase. Molecular docking estimated the interaction energies of amino acid residues with either lactose or succinic anhydride, showing that Lys(138) is the most likely to react with both. Affinity chromatography demonstrated that succinylated beta-lactoglobulin diminished its ability to bind to the enzyme. Furthermore, when activity was measured in the presence of succinylated beta-lactoglobulin, its activating effect was lost. Since succinylation specifically blocks Lys epsilon-amino groups, their loss very likely causes the disappearance of the activating effect. Results show that the activating effect of beta-lactoglobulin on beta-galactosidase activity is due to the interaction between both proteins and that this interaction is very likely to occur through the Lys epsilon-amino groups of beta-lactoglobulin.
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- 2008
9. Hydrophobic Repacking of the Dimer Interface of Triosephosphate Isomerase by in Silico Design and Directed Evolution
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Lenin Domínguez-Ramírez, D. Alejandro Fernández-Velasco, and Mariana Peimbert
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Models, Molecular ,Protein Folding ,Stereochemistry ,In silico ,Dimer ,Saccharomyces cerevisiae ,Biochemistry ,Catalysis ,Dissociation (chemistry) ,Accessible surface area ,Triosephosphate isomerase ,chemistry.chemical_compound ,Computer Simulation ,biology ,Active site ,Directed evolution ,Protein Structure, Tertiary ,Crystallography ,Monomer ,chemistry ,Mutation ,biology.protein ,Directed Molecular Evolution ,Dimerization ,Hydrophobic and Hydrophilic Interactions ,Triose-Phosphate Isomerase - Abstract
Triosephosphate isomerase from Saccharomyces cerevisiae (wt-TIM) is an obligated homodimer. The interface of wt-TIM is formed by 34 residues. In the native dimer, each monomer buries nearly 2600 A 2 of accessible surface area (ASA), and 58.4% of the interface ASA is hydrophobic. We determined the thermodynamic and functional consequences of increasing the hydrophobic character of the wt-TIM interface. Mutations were restricted to a cluster of five nonconserved residues located far from the active site. Two different approaches, in silico design and directed evolution, were employed. In both methodologies, the obtained proteins were soluble, dimeric, and compact. In silico-designed proteins are very stable dimers that bind substrate with a wild-type-like K m ; albeit, they exhibited a very low k cat . Proteins obtained from directed evolution experiments show wild-type-like catalytic activity, while their stability is decreased. Hydrophobic replacements at the interface produced a remarkable shift in the dissociation step. For wt-TIM and for TIMs obtained by directed evolution, dissociation was observed in the first transition, with C 1/2 values ranging from 0.58 to 0.024 M GdnHCl, whereas for TIMs generated by in silico design, dissociation occurred in the last transition, with C 1/2 values ranging form 3.01 to 3.65 M GdnHCl. For the latter mutants, the stabilization of the interface changed the equilibrium transitions to a novel four-state process with two dimeric intermediates. The change in the intermediate nature suggests that the relative stabilities of different folding units are similar so that subtle alterations in their stability produce a total transformation of the folding pathway.
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- 2008
10. A hinge of the endogeneous ATP synthase inhibitor protein: The link between inhibitory and anchoring domains
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Armando Gómez-Puyou, Lenin Domínguez-Ramírez, and M. Tuena de Gómez-Puyou
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Protein subunit ,Amino Acid Motifs ,Molecular Sequence Data ,Mitochondrion ,Biochemistry ,Structural Biology ,ATP synthase gamma subunit ,ATP hydrolysis ,Animals ,Humans ,Amino Acid Sequence ,Databases, Protein ,Molecular Biology ,chemistry.chemical_classification ,ATP synthase ,biology ,Proteins ,Inhibitor protein ,Models, Theoretical ,Protein Structure, Tertiary ,Protein Subunits ,Enzyme ,chemistry ,biology.protein ,Cattle ,Dimerization ,Sequence Alignment ,ATP synthase alpha/beta subunits - Abstract
The ATP synthase of bovine heart mitochondria possesses a regulatory subunit called the endogenous inhibitory protein (IF1). This subunit regulates the catalytic activity of the F1 sector in the mitochondrial inner membrane. When ΔμH+ falls, IF1 binds to the enzyme and inhibits ATP hydrolysis. On the other hand, the establishment of a ΔμH+ induces the release of the inhibitory action of IF1, allowing ATP synthesis to proceed. IF1 is also involved in the dimerization of soluble F1. Dynamic domain analysis and normal mode analysis of the reported crystallographic structure of IF1 revealed that it has an effective hinge formed by residues 46–52. Molecular dynamics data of a 27 residue fragment confirmed the existence of the hinge. The hinge may act as a regulatory region that links the inhibitory and anchoring domains of IF1. The residues assigned to the hinge are conserved between mammals, but not in other species, such as yeasts. Likewise, unlike the heart inhibitor, the yeast protein does not have the residues that allow it to form stable dimers through coiled-coil interactions. Collectively, the data suggest that the hinge and the dimerization domain of the inhibitor protein from bovine heart are related to its ability to form stable dimers and to interact with other subunits of the ATP synthase. Proteins 2006. © 2006 Wiley-Liss, Inc.
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- 2006
11. The inhibitor protein of the F1F0-ATP synthase is associated to the external surface of endothelial cells
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Paulina Cortés-Hernández, Marietta Tuena de Gómez-Puyou, Armando Gómez-Puyou, Alejandro Zentella-Dehesa, Adriana Estrada-Bernal, José J. García, Lenin Domínguez-Ramírez, and Delina G. Montes-Sánchez
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Umbilical Veins ,Biophysics ,Mitochondrion ,Biochemistry ,Antibodies ,Flow cytometry ,law.invention ,Confocal microscopy ,law ,medicine ,Humans ,Molecular Biology ,Cells, Cultured ,Microscopy, Confocal ,ATP synthase ,biology ,medicine.diagnostic_test ,Tumor Necrosis Factor-alpha ,Cell Membrane ,Endothelial Cells ,Proteins ,Cell Biology ,Inhibitor protein ,Mitochondrial Proton-Translocating ATPases ,Cell biology ,Protein Subunits ,Membrane ,Solubility ,biology.protein ,Antibody ,Function (biology) ,Protein Binding - Abstract
The ATPase inhibitor protein (IP) of mitochondria was detected in the plasma membrane of living endothelial cells by flow cytometry, competition assays, and confocal microscopy of cells exposed to IP antibodies. The plasma membranes of endothelial cells also possess beta-subunits of the mitochondrial ATPase. Plasma membranes have the capacity to bind exogenous IP. TNF-alpha decreases the level of beta-subunits and increases the amount of IP, indicating that the ratio of IP to beta-subunit exhibits significant variations. Therefore, it is probable that the function of IP in the plasma membrane of endothelial cells is not limited to regulation of catalysis.
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- 2005
12. Interconversion Between Dimers and Monomers of Endogenous Mitochondrial F1-Inhibitor Protein Complexes and the Release of the Inhibitor Protein. Spectroscopic Characteristics of the Complexes
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Hugo Nájera, Georgina Garza-Ramos, Marietta Tuena de Gómez-Puyou, Armando Gómez-Puyou, Guillermo Mendoza-Hernández, and Lenin Domínguez-Ramírez
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Protein Conformation ,Physiology ,Stereochemistry ,Size-exclusion chromatography ,Tryptophan ,Proteins ,Cell Biology ,Inhibitor protein ,Fluorescence ,Mitochondria, Heart ,Enzyme Activation ,chemistry.chemical_compound ,Monomer ,chemistry ,Biochemistry ,Chromatography, Gel ,Animals ,Bioorganic chemistry ,Cattle ,Submitochondrial particle ,Tyrosine ,Binding site ,Dimerization - Abstract
The F1-inhibitor protein complex (F1-IP) was purified from heart submitochondrial particles. Size exclusion chromatography of the endogenous complex showed that it contains dimers (D) and monomers (M) of F1-IP. Further chromatographic analysis showed that D and M interconvert. At high protein concentrations, the interconversion reaction is shifted toward the D species. The release of the inhibiting action of IP is faster at low than at high protein concentrations. During activation of F1, the M species accumulates through a process that is faster than the release of IP from F1. These findings indicate that the activation of F1-IP involves the transformation of D into M, which subsequently loses IP. The spectroscopic characteristics of D, M, and free F1 show that the binding of IP and dimerization modifies the fluorescence intensity of tyrosine residues and that of the single tryptophan of F1 which is far from the IP binding site.
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- 2004
13. Equilibrium between monomeric and dimeric mitochondrial F1-inhibitor protein complexes
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Lenin Domínguez-Ramírez, Armando Gómez-Puyou, M. Tuena de Gómez-Puyou, A. Carabez-Trejo, and Guillermo Mendoza-Hernández
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Endogenous complex ,Dimer ,Size-exclusion chromatography ,Biophysics ,Calcium-Transporting ATPases ,Mitochondrion ,Biochemistry ,Mitochondria, Heart ,law.invention ,chemistry.chemical_compound ,Structural Biology ,law ,Genetics ,Animals ,Molecular Biology ,F1-ATPase ,Proteins ,Cell Biology ,Inhibitor protein ,Hydrogen-Ion Concentration ,Proton-Translocating ATPases ,Crystallography ,Monomer ,chemistry ,Solubilization ,Cattle ,Electron microscope ,Dimerization - Abstract
Mg-ATP particles from bovine heart mitochondria have more than 95% of their F1 in complex with the inhibitor protein (IF1). The F1–IF1 complex was solubilized and purified. The question addressed was if this naturally occurring complex existed as monomers or dimers. Size exclusion chromatography and electron microscopy showed that most of the purified F1–IF1 complex was a dimer of two F1–IF1. As determined by the former method, the relative concentrations of dimeric and monomeric F1–IF1 depended on the concentration of protein that was applied to the column. Apparently, there is an equilibrium between the two forms of F1–IF1.
- Published
- 2001
14. Structural Alterations and Inhibition of Unisite and Multisite ATP Hydrolysis in Soluble Mitochondrial F1 by Guanidinium Chloride
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Armando Gómez-Puyou, M. Tuena de Gómez-Puyou, Horacio Reyes-Vivas, and Lenin Domínguez-Ramírez
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Guanidinium chloride ,Protein Denaturation ,ATPase ,Mitochondrion ,Biochemistry ,Catalysis ,Mitochondria, Heart ,chemistry.chemical_compound ,Hydrolysis ,Adenosine Triphosphate ,Adenine nucleotide ,ATP hydrolysis ,Animals ,Urea ,Guanidine ,Binding Sites ,Dose-Response Relationship, Drug ,biology ,Adenine Nucleotides ,Proton-Translocating ATPases ,Solubility ,chemistry ,biology.protein ,Cattle ,Phosphorus Radioisotopes ,Cysteine - Abstract
The effect of guanidinium chloride (GdnHCl) on the ATPase activity and structure of soluble mitochondrial F1 was studied. At high ATP concentrations, hydrolysis is carried by the three catalytic sites of F1; this reaction was strongly inhibited by GdnHCl concentrations of50 mM. With substoichiometric ATP concentrations, hydrolysis is catalyzed exclusively by the site with the highest affinity. Under these conditions, ATP binding and hydrolysis took place with GdnHCl concentrations of100 mM; albeit at the latter concentration, the rate of hydrolysis of bound ATP was lower. Similar results were obtained with urea, although nearly 10-fold higher concentrations were required to inhibit multisite hydrolysis. GdnHCl inhibited multisite ATPase activity by diminishing the V(max) of the reaction without significant alterations of the Km for MgATP. GdnHCl prevented the effect of excess ATP on hydrolysis of ATP that was already bound to the high-affinity catalytic site. With and without 100 mM GdnHCl and 100 microM [3H]ATP in the medium, F1 bound 1.6 and 2 adenine nucleotides per F1, respectively. The effect of GdnHCl on some structural features of F1 was also examined. GdnHCl at concentrations that inhibit multisite ATP hydrolysis did not affect the exposure of the cysteines of F1, nor its intrinsic fluorescence. With 100 mM GdnHCl, a concentration at which unisite ATP hydrolysis was still observed, 0.7 cysteine per F1 became solvent-exposed and small changes in its intrinsic fluorescence of F1 were detected. GdnHCl concentrations on the order of 500 mM were required to induce important decreases in intrinsic fluorescence. These changes accompanied inhibition of unisite ATP hydrolysis. The overall data indicate that increasing concentrations of GdnHCl bring about distinct and sequential alterations in the function and structure of F1. With respect to the function of F1, the results show that at low GdnHCl concentrations, only the high-affinity site expresses catalytic activity, and that inhibition of multisite catalysis is due to alterations in the transmission of events between catalytic sites.
- Published
- 2001
15. Interactions of subunits Asa2, Asa4 and Asa7 in the peripheral stalk of the mitochondrial ATP synthase of the chlorophycean alga Polytomella sp
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Claire Remacle, Angela Downie-Velasco, Lilia Colina-Tenorio, Lenin Domínguez-Ramírez, Pierre Cardol, Diego González-Halphen, Miriam Vázquez-Acevedo, Héctor Miranda-Astudillo, and Araceli Cano-Estrada
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Models, Molecular ,Protein subunit ,Dimeric mitochondrial complex V ,Biophysics ,Chlorophycean algae ,Chlamydomonas reinhardtii ,Biochemistry ,Affinity chromatography ,F1FO-ATP synthase peripheral-stalk ,Computer Simulation ,Polytomella sp ,Amino Acid Sequence ,Inner mitochondrial membrane ,chemistry.chemical_classification ,Asa subunits ,ATP synthase ,biology ,Polytomella ,Cell Biology ,Mitochondrial Proton-Translocating ATPases ,biology.organism_classification ,Mitochondria ,Protein Subunits ,Enzyme ,Stalk ,chemistry ,Multiprotein Complexes ,Mitochondrial Membranes ,biology.protein ,Electrophoresis, Polyacrylamide Gel ,Peptides ,Volvocida ,Dimerization - Abstract
Mitochondrial F1FO-ATP synthase of chlorophycean algae is a complex partially embedded in the inner mitochondrial membrane that is isolated as a highly stable dimer of 1600kDa. It comprises 17 polypeptides, nine of which (subunits Asa1 to 9) are not present in classical mitochondrial ATP synthases and appear to be exclusive of the chlorophycean lineage. In particular, subunits Asa2, Asa4 and Asa7 seem to constitute a section of the peripheral stalk of the enzyme. Here, we over-expressed and purified subunits Asa2, Asa4 and Asa7 and the corresponding amino-terminal and carboxy-terminal halves of Asa4 and Asa7 in order to explore their interactions in vitro, using immunochemical techniques, blue native electrophoresis and affinity chromatography. Asa4 and Asa7 interact strongly, mainly through their carboxy-terminal halves. Asa2 interacts with both Asa7 and Asa4, and also with subunit α in the F1 sector. The three Asa proteins form an Asa2/Asa4/Asa7 subcomplex. The entire Asa7 and the carboxy-terminal half of Asa4 seem to be instrumental in the interaction with Asa2. Based on these results and on computer-generated structural models of the three subunits, we propose a model for the Asa2/Asa4/Asa7 subcomplex and for its disposition in the peripheral stalk of the algal ATP synthase.
- Published
- 2013
16. Conformational dynamics of L-lysine, L-arginine, L-ornithine binding protein reveals ligand-dependent plasticity
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Daniel-Adriano Silva, Lenin Domínguez-Ramírez, Arturo Rojo-Domínguez, and Alejandro Sosa-Peinado
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Ornithine ,Salmonella typhimurium ,Stereochemistry ,Protein Conformation ,Molecular Dynamics Simulation ,Arginine ,Biochemistry ,Molecular dynamics ,Protein structure ,Bacterial Proteins ,Structural Biology ,Amino Acids ,Molecular Biology ,Conformational ensembles ,Histidine ,Principal Component Analysis ,Hydrogen bond ,Chemistry ,Binding protein ,Lysine ,Hydrogen Bonding ,Ligand (biochemistry) ,Crystallography ,Periplasmic Binding Proteins ,Carrier Proteins ,Binding domain - Abstract
The molecular basis of multiple ligand binding affinity for amino acids in periplasmic binding proteins (PBPs) and in the homologous domain for class C G-protein coupled receptors is an unsolved question. Here, using unrestrained molecular dynamic simulations, we studied the ligand binding mechanism present in the L-lysine, L-arginine, L-ornithine binding protein. We developed an analysis based on dihedral angles for the description of the conformational changes upon ligand binding. This analysis has an excellent correlation with each of the two main movements described by principal component analysis (PCA) and it's more convenient than RMSD measurements to describe the differences in the conformational ensembles observed. Furthermore, an analysis of hydrogen bonds showed specific interactions for each ligand studied as well as the ligand interaction with the aromatic residues Tyr-14 and Phe-52. Using uncharged histidine tautomers, these interactions are not observed. On the basis of these results, we propose a model in which hydrogen bond interactions place the ligand in the correct orientation to induce a cation-π interaction with Tyr-14 and Phe-52 thereby stabilizing the closed state. Our results also show that this protein adopts slightly different closed conformations to make available specific hydrogen bond interactions for each ligand thus, allowing a single mechanism to attain multiple ligand specificity. These results shed light on the experimental evidence for ligand-dependent conformational plasticity not explained by the previous crystallographic data.
- Published
- 2010
17. The beta subunit of the heterotrimeric G protein triggers the Kluyveromyces lactis pheromone response pathway in the absence of the gamma subunit
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Laura Ongay-Larios, Rocio Navarro-Olmos, Roberto Coria, Lenin Domínguez-Ramírez, Laura Kawasaki, and Rosario Pérez-Molina
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Models, Molecular ,Saccharomyces cerevisiae Proteins ,Protein subunit ,GTP-Binding Protein alpha Subunits ,Gi alpha subunit ,Molecular Sequence Data ,GTP-Binding Protein beta Subunits ,Saccharomyces cerevisiae ,Pheromones ,Kluyveromyces ,Heterotrimeric G protein ,GTP-Binding Protein gamma Subunits ,Two-Hybrid System Techniques ,Amino Acid Sequence ,Molecular Biology ,Kluyveromyces lactis ,biology ,Cell Biology ,Articles ,biology.organism_classification ,Signaling ,Protein Structure, Tertiary ,G beta-gamma complex ,Biochemistry ,Mutagenesis ,Sequence Alignment ,Signal Transduction - Abstract
The Gγ subunit of the heterotrimeric G protein is not required to trigger the mating pathway in K. lactis. When the Gγ subunit is missing, the Gα subunit carry Gβ to the plasma membrane and the pheromone pathway is then activated by the Gα/Gβ heterodimer., The Kluyveromyces lactis heterotrimeric G protein is a canonical Gαβγ complex; however, in contrast to Saccharomyces cerevisiae, where the Gγ subunit is essential for mating, disruption of the KlGγ gene yielded cells with almost intact mating capacity. Expression of a nonfarnesylated Gγ, which behaves as a dominant-negative in S. cerevisiae, did not affect mating in wild-type and ΔGγ cells of K. lactis. In contrast to the moderate sterility shown by the single ΔKlGα, the double ΔKlGα ΔKlGγ mutant displayed full sterility. A partial sterile phenotype of the ΔKlGγ mutant was obtained in conditions where the KlGβ subunit interacted defectively with the Gα subunit. The addition of a CCAAX motif to the C-end of KlGβ, partially suppressed the lack of both KlGα and KlGγ subunits. In cells lacking KlGγ, the KlGβ subunit cofractionated with KlGα in the plasma membrane, but in the ΔKlGα ΔKlGγ strain was located in the cytosol. When the KlGβ-KlGα interaction was affected in the ΔKlGγ mutant, most KlGβ fractionated to the cytosol. In contrast to the generic model of G-protein function, the Gβ subunit of K. lactis has the capacity to attach to the membrane and to activate mating effectors in absence of the Gγ subunit.
- Published
- 2009
18. Different regions of Mlc and NagC, homologous transcriptional repressors controlling expression of the glucose and N-acetylglucosamine phosphotransferase systems in Escherichia coli, are required for inducer signal recognition
- Author
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Carole Pennetier, Jacqueline Plumbridge, and Lenin Domínguez-Ramírez
- Subjects
Models, Molecular ,Operator Regions, Genetic ,Transcription, Genetic ,Molecular Sequence Data ,Gene Dosage ,Repressor ,Electrophoretic Mobility Shift Assay ,macromolecular substances ,Biology ,Microbiology ,Acetylglucosamine ,chemistry.chemical_compound ,Escherichia coli ,Point Mutation ,Inducer ,Amino Acid Sequence ,Binding site ,Structural motif ,Molecular Biology ,Transcription factor ,Helix-Turn-Helix Motifs ,Sequence Deletion ,Escherichia coli Proteins ,Phosphotransferases ,Protein Structure, Tertiary ,DNA binding site ,Glucose binding ,Repressor Proteins ,Glucose ,Biochemistry ,chemistry ,Sequence Alignment ,DNA ,Plasmids ,Signal Transduction ,Transcription Factors - Abstract
Summary Mlc and NagC are two homologous transcription factors which bind to similar DNA targets but for which the inducing signals and mechanisms of activation are very different. Displacing Mlc from its DNA binding sites necessitates its sequestration to the inner membrane via an interaction with PtsG (EIICBGlc), while NagC is displaced from its DNA targets by interacting with GlcNAc6P. We have isolated mutations in both proteins which prevent the inactivation of the repressors by growth on glucose or GlcNAc. These mutations are located in different and specific regions of each protein. For Mlc changes at the C-terminal make it a constitutive repressor and also prevent it from binding to EIIBGlc. Mutations in NagC, at positions which form a structural motif resembling a glucose binding site in Mlc, produce permanently repressing forms of NagC, suggesting that this motif forms a GlcNAc6P binding site in NagC. The pattern of repression by chimeric proteins of NagC and Mlc confirms the importance of the C-terminal region of Mlc for both repression and inducer binding and demonstrate that the helix–turn–helix DNA-binding motif is not sufficient to determine the specificity of interaction of the repressor with DNA.
- Published
- 2007
19. Analysis of the antimicrobial activities of a chemokine-derived peptide (CDAP-4) on Pseudomonas aeruginosa
- Author
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Gloria Soldevila, Lenin Domínguez-Ramírez, Eduardo A. García-Zepeda, Guillermo Mendoza-Hernández, Francisco J. Martinez-Becerra, Yolanda López-Vidal, and Daniel-Adriano Silva
- Subjects
Chemokine ,Antimicrobial peptides ,Molecular Sequence Data ,Biophysics ,Peptide ,medicine.disease_cause ,Biochemistry ,Microbiology ,Microscopy, Electron, Transmission ,medicine ,Amino Acid Sequence ,CCL13 ,Molecular Biology ,Peptide sequence ,Chemokine CCL3 ,chemistry.chemical_classification ,biology ,Pseudomonas aeruginosa ,Pseudomonas ,Cell Biology ,biology.organism_classification ,Antimicrobial ,Anti-Bacterial Agents ,chemistry ,Chemokines, CC ,biology.protein ,Peptides - Abstract
Chemokines are key molecules involved in the control of leukocyte trafficking. Recently, a novel function as antimicrobial proteins has been described. CCL13 is the only member of the MCP chemokine subfamily displaying antimicrobial activity. To determine the key residues involved in its antimicrobial activity, CCL13 derived peptides were synthesized and tested against several bacterial strains, including Pseudomonas aeruginosa. One of these peptides, corresponding to the C-terminal region of CCL13 (CDAP-4) displayed good antimicrobial activity. Electron microscopy studies revealed remarkable morphological changes after CDAP-4 treatment. By computer modeling, CDAP-4 in alpha helical configuration generated a positive electrostatic potential that extended beyond the surface of the molecule. This feature is similar to other antimicrobial peptides. Altogether, these findings indicate that the antimicrobial activity was displayed by CCL13 resides to some extent at the C-terminal region. Furthermore, CDAP-4 could be considered a good antimicrobial candidate with a potential use against pathogens including P. aeruginosa.
- Published
- 2007
20. New Insights on the Mechanism of the K+-Independent Activity of Crenarchaeota Pyruvate Kinases
- Author
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Gustavo De la Vega-Ruíz, Carlos Guerrero-Mendiola, Alfredo Torres-Larios, Leticia Ramírez-Silva, José J. García-Trejo, Héctor Riveros-Rosas, Gloria Hernández-Alcántara, and Lenin Domínguez-Ramírez
- Subjects
Science ,Archaeal Proteins ,Molecular Sequence Data ,Pyruvate Kinase ,Lysine ,PKM2 ,Catalysis ,Serine ,Allosteric Regulation ,Animals ,Amino Acid Sequence ,Muscle, Skeletal ,Phylogeny ,chemistry.chemical_classification ,Multidisciplinary ,Calorimetry, Differential Scanning ,biology ,Kinase ,Crenarchaeota ,Correction ,Substrate (chemistry) ,Recombinant Proteins ,Enzyme assay ,Protein Structure, Tertiary ,Kinetics ,Enzyme ,chemistry ,Biochemistry ,Potassium ,biology.protein ,Medicine ,Rabbits ,Sequence Alignment ,Pyruvate kinase ,Research Article - Abstract
Eukarya pyruvate kinases have glutamate at position 117 (numbered according to the rabbit muscle enzyme), whereas in Bacteria have either glutamate or lysine and in Archaea have other residues. Glutamate at this position makes pyruvate kinases K+-dependent, whereas lysine confers K+-independence because the positively charged residue substitutes for the monovalent cation charge. Interestingly, pyruvate kinases from two characterized Crenarchaeota exhibit K+-independent activity, despite having serine at the equivalent position. To better understand pyruvate kinase catalytic activity in the absence of K+ or an internal positive charge, the Thermofilum pendens pyruvate kinase (valine at the equivalent position) was characterized. The enzyme activity was K+-independent. The kinetic mechanism was random order with a rapid equilibrium, which is equal to the mechanism of the rabbit muscle enzyme in the presence of K+ or the mutant E117K in the absence of K+. Thus, the substrate binding order of the T. pendens enzyme was independent despite lacking an internal positive charge. Thermal stability studies of this enzyme showed two calorimetric transitions, one attributable to the A and C domains (Tm of 99.2°C), and the other (Tm of 105.2°C) associated with the B domain. In contrast, the rabbit muscle enzyme exhibits a single calorimetric transition (Tm of 65.2°C). The calorimetric and kinetic data indicate that the B domain of this hyperthermophilic enzyme is more stable than the rest of the protein with a conformation that induces the catalytic readiness of the enzyme. B domain interactions of pyruvate kinases that have been determined in Pyrobaculum aerophilum and modeled in T. pendens were compared with those of the rabbit muscle enzyme. The results show that intra- and interdomain interactions of the Crenarchaeota enzymes may account for their higher B domain stability. Thus the structural arrangement of the T. pendens pyruvate kinase could allow charge-independent catalysis.
- Published
- 2015
21. Disulfide bridges in the mesophilic triosephosphate isomerase from Giardia lamblia are related to oligomerization and activity
- Author
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Gabriel López-Velázquez, Horacio Reyes-Vivas, Sergio Enríquez-Flores, Lenin Domínguez-Ramírez, Adelaida Díaz, Ignacio de la Mora-de la Mora, Gloria Hernández-Alcántara, Jorge Peon, and Guillermo Mendoza-Hernández
- Subjects
Stereochemistry ,Isomerase ,Crystallography, X-Ray ,Ligands ,Protein Structure, Secondary ,Triosephosphate isomerase ,Hydrophobic effect ,Structure-Activity Relationship ,Protein structure ,Structural Biology ,Animals ,Cysteine ,Disulfides ,Trophozoites ,Protein disulfide-isomerase ,Protein Structure, Quaternary ,Molecular Biology ,chemistry.chemical_classification ,Hydrogen bond ,Oocysts ,Substrate (chemistry) ,Kinetics ,Protein Subunits ,Protein Transport ,chemistry ,Biochemistry ,Thiol ,Chromatography, Gel ,Mutant Proteins ,Giardia lamblia ,Dimerization ,Copper ,Triose-Phosphate Isomerase - Abstract
Triosephosphate isomerase from the mesophile Giardia lamblia (GlTIM) is the only known TIM with natural disulfide bridges. We previously found that oxidized and reduced thiol states of GlTIM are involved in the interconversion between native dimers and higher oligomeric species, and in the regulation of enzymatic activity. Here, we found that trophozoites and cysts have different oligomeric species of GlTIM and complexes of GlTIM with other proteins. Our data indicate that the internal milieu of G. lamblia is favorable for the formation of disulfide bonds. Enzyme mutants of the three most solvent exposed Cys of GlTIM (C202A, C222A, and C228A) were prepared to ascertain their contribution to oligomerization and activity. The data show that the establishment of a disulfide bridge between two C202 of two dimeric GlTIMs accounts for multimerization. In addition, we found that the establishment of an intramonomeric disulfide bond between C222 and C228 abolishes catalysis. Multimerization and inactivation are both reversed by reducing conditions. The 3D structure of the C202A GlTIM was solved at 2.1 A resolution, showing that the environment of the C202 is prone to hydrophobic interactions. Molecular dynamics of an in silico model of GlTIM when the intramonomeric disulfide bond is formed, showed that S216 is displaced 4.6 A from its original position, causing loss of hydrogen bonds with residues of the active-site loop. This suggests that this change perturb the conformational state that aligns the catalytic center with the substrate, inducing enzyme inactivation.
- Published
- 2006
22. Effect of denaturants on multisite and unisite ATP hydrolysis by bovine heart submitochondrial particles with and without inhibitor protein
- Author
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Marietta Tuena de Gómez-Puyou, Armando Gómez-Puyou, Gerardo Pérez-Hernández, and Lenin Domínguez-Ramírez
- Subjects
Protein Denaturation ,Hydrochloride ,Submitochondrial Particles ,Biophysics ,Biochemistry ,Mitochondria, Heart ,Catalysis ,Hydrolysis ,chemistry.chemical_compound ,Adenosine Triphosphate ,ATP hydrolysis ,Atpase activity ,Animals ,Submitochondrial particle ,Molecular Biology ,Guanidine ,chemistry.chemical_classification ,Uncoupling Agents ,Proteins ,Inhibitor protein ,Aurovertins ,Enzyme Activation ,Proton-Translocating ATPases ,Enzyme ,chemistry ,Cattle - Abstract
The effect of guanidinium hydrochloride (GdnHCl) on multisite and unisite ATPase activity by F0F1 of submitochondrial particles from bovine hearts was studied. In particles without control by the inhibitor protein, 50 mM GdnHCl inhibited multisite hydrolysis by about 85%; full inhibition required around 500 mM. In the range of 500–650 mM, GdnHCl enhanced the rate of unisite catalysis by promoting product release; it also increased the rate of hydrolysis of ATP bound to the catalytic site without GdnHCl. GdnHCl diminished the affinity of the enzyme for aurovertin. The effects of GdnHCl were irreversible. The results suggest that disruption of intersubunit contacts in F0F1 abolishes multisite hydrolysis and stimulates of unisite hydrolysis. Particles under control by the inhibitor protein were insensitive to concentrations of GdnHCl that induce the aforementioned alterations of F0F1 free of inhibitor protein, indicating that the protein stabilizes the global structure of particulate F1.
- Published
- 2005
23. β-Lactoglobulin's Conformational Requirements for Ligand Binding at the Calyx and the Dimer Interphase: a Flexible Docking Study
- Author
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Elizabeth Del Moral-Ramírez, Paulina Cortés-Hernández, Mariano García-Garibay, Judith Jiménez-Guzmán, and Lenin Domínguez-Ramírez
- Subjects
Stereochemistry ,Science ,Dimer ,Molecular Sequence Data ,Protein design ,Lactose ,Lactoglobulins ,Ligands ,Protein Structure, Secondary ,chemistry.chemical_compound ,Fatty acid binding ,Side chain ,Animals ,Amino Acid Sequence ,Binding site ,Protein Structure, Quaternary ,Cholecalciferol ,Binding Sites ,Multidisciplinary ,Hydrogen bond ,Chemistry ,Computational Biology ,Ligand (biochemistry) ,Molecular Docking Simulation ,Biochemistry ,Docking (molecular) ,Medicine ,Cattle ,Protein Multimerization ,Hydrophobic and Hydrophilic Interactions ,Protein Binding ,Research Article - Abstract
β-lactoglobulin (BLG) is an abundant milk protein relevant for industry and biotechnology, due significantly to its ability to bind a wide range of polar and apolar ligands. While hydrophobic ligand sites are known, sites for hydrophilic ligands such as the prevalent milk sugar, lactose, remain undetermined. Through the use of molecular docking we first, analyzed the known fatty acid binding sites in order to dissect their atomistic determinants and second, predicted the interaction sites for lactose with monomeric and dimeric BLG. We validated our approach against BLG structures co-crystallized with ligands and report a computational setup with a reduced number of flexible residues that is able to reproduce experimental results with high precision. Blind dockings with and without flexible side chains on BLG showed that: i) 13 experimentally-determined ligands fit the calyx requiring minimal movement of up to 7 residues out of the 23 that constitute this binding site. ii) Lactose does not bind the calyx despite conformational flexibility, but binds the dimer interface and an alternate Site C. iii) Results point to a probable lactolation site in the BLG dimer interface, at K141, consistent with previous biochemical findings. In contrast, no accessible lysines are found near Site C. iv) lactose forms hydrogen bonds with residues from both monomers stabilizing the dimer through a claw-like structure. Overall, these results improve our understanding of BLG's binding sites, importantly narrowing down the calyx residues that control ligand binding. Moreover, our results emphasize the importance of the dimer interface as an insufficiently explored, biologically relevant binding site of particular importance for hydrophilic ligands. Furthermore our analyses suggest that BLG is a robust scaffold for multiple ligand-binding, suitable for protein design, and advance our molecular understanding of its ligand sites to a point that allows manipulation to control binding.
- Published
- 2013
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