Back to Search
Start Over
Occurrence and stability of hetero-hexamer associations formed by β-carboxysome CcmK shell components
- Source :
- PLoS ONE, Vol 14, Iss 10, p e0223877 (2019), PLoS ONE, PLoS ONE, Public Library of Science, 2019, 14 (10), pp.e0223877. ⟨10.1371/journal.pone.0223877⟩, PLoS ONE, 2019, 14 (10), pp.e0223877. ⟨10.1371/journal.pone.0223877⟩, 'PloS One ', vol: 14, pages: e0223877-1-e0223877-28 (2019), PLoS ONE, 14 (10), PLoS ONE, Public Library of Science, 2019, ⟨10.1371/journal.pone.0223877⟩
- Publication Year :
- 2019
- Publisher :
- Public Library of Science (PLoS), 2019.
-
Abstract
- The carboxysome is a bacterial micro-compartment (BMC) subtype that encapsulates enzymatic activities necessary for carbon fixation. Carboxysome shells are composed of a relatively complex cocktail of proteins, their precise number and identity being species dependent. Shell components can be classified in two structural families, the most abundant class associating as hexamers (BMC-H) that are supposed to be major players for regulating shell permeability. Up to recently, these proteins were proposed to associate as homo-oligomers. Genomic data, however, demonstrated the existence of paralogs coding for multiple shell subunits. Here, we studied cross-association compatibilities among BMC-H CcmK proteins of Synechocystis sp. PCC6803. Co-expression in Escherichia coli proved a consistent formation of hetero-hexamers combining CcmK1 and CcmK2 or, remarkably, CcmK3 and CcmK4 subunits. Unlike CcmK1/K2 hetero-hexamers, the stoichiometry of incorporation of CcmK3 in associations with CcmK4 was low. Cross-interactions implicating other combinations were weak, highlighting a structural segregation of the two groups that could relate to gene organization. Sequence analysis and structural models permitted the localization of interactions that would favor formation of CcmK3/K4 hetero-hexamers. The crystallization of these CcmK3/K4 associations conducted to the elucidation of a structure corresponding to the CcmK4 homo-hexamer. Yet, subunit exchange could not be demonstrated in vitro. Biophysical measurements showed that hetero-hexamers are thermally less stable than homo-hexamers, and impeded in forming larger assemblies. These novel findings are discussed within the context of reported data to propose a functional scenario in which minor CcmK3/K4 incorporation in shells would introduce sufficient local disorder as to allow shell remodeling necessary to adapt rapidly to environmental changes.<br />PLoS ONE, 14 (10)<br />ISSN:1932-6203
- Subjects :
- 0106 biological sciences
Models, Molecular
[SDV.BIO]Life Sciences [q-bio]/Biotechnology
[SDV]Life Sciences [q-bio]
Plasma protein binding
Random hexamer
Crystallography, X-Ray
Protein Engineering
medicine.disease_cause
01 natural sciences
Biochemistry
Electricity
Nucleic Acids
Chemical Precipitation
Macromolecular Engineering
ComputingMilieux_MISCELLANEOUS
0303 health sciences
Multidisciplinary
Crystallography
Protein Stability
Chemistry
Physics
Monomers
Chemical Reactions
Synechocystis
Condensed Matter Physics
Stoichiometry
[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biomolecules [q-bio.BM]
Carboxysome
Synechocystis sp
Physical Sciences
Crystal Structure
Engineering and Technology
Thermodynamics
Medicine
Synthetic Biology
Crystallization
Research Article
Protein Binding
Gene Organization
Sequence analysis
Protein subunit
Science
Shell (structure)
Context (language use)
Bioengineering
03 medical and health sciences
Bacterial Proteins
Electrostatics
Genetics
Escherichia coli
medicine
Solid State Physics
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
Operons
030304 developmental biology
Binding Sites
030306 microbiology
Biology and Life Sciences
Protein engineering
DNA
Polymer Chemistry
Synthetic Bioengineering
Multiprotein Complexes
Signal Processing
Biophysics
Protein Multimerization
010606 plant biology & botany
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Volume :
- 14
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- PLoS ONE
- Accession number :
- edsair.doi.dedup.....f3da1b79ef93e3e5b2f08c24e981bff6
- Full Text :
- https://doi.org/10.1371/journal.pone.0223877⟩