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Following ligand migration pathways from picoseconds to milliseconds in type II truncated hemoglobin from Thermobifida fusca
- Source :
- PLoS ONE, PLoS ONE, Public Library of Science, 2012, 7 (7), pp.e39884. ⟨10.1371/journal.pone.0039884⟩, PloS one 7 (2012): e39884–e39884. doi:10.1371/journal.pone.0039884, info:cnr-pdr/source/autori:Marcelli Agnese [ 1 ] ; Abbruzzetti Stefania [ 2 ] ; Bustamante Juan Pablo [ 3 ] ; Feis Alessandro [ 4 ] ; Bonamore Alessandra [ 5 ] ; Boffi Alberto [ 5 ] ; Gellini Cristina [ 4 ] ; Salvi Pier Remigio [ 4 ] ; Estrin Dario A. [ 3 ] ; Bruno Stefano [ 6 ] ; Viappiani Cristiano [ 2 ] ; Foggi Paolo [ 1,7,8 ]/titolo:Following Ligand Migration Pathways from Picoseconds to Milliseconds in Type II Truncated Hemoglobin from Thermobifida fusca/doi:10.1371%2Fjournal.pone.0039884/rivista:PloS one/anno:2012/pagina_da:e39884/pagina_a:e39884/intervallo_pagine:e39884–e39884/volume:7, PLoS ONE, Vol 7, Iss 7, p e39884 (2012), CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET
- Publication Year :
- 2012
- Publisher :
- HAL CCSD, 2012.
-
Abstract
- CO recombination kinetics has been investigated in the type II truncated hemoglobin from Thermobifida fusca (Tf-trHb) over more than 10 time decades (from 1 ps to 100 ms) by combining femtosecond transient absorption, nanosecond laser flash photolysis and optoacoustic spectroscopy. Photolysis is followed by a rapid geminate recombination with a time constant of 2 ns representing almost 60% of the overall reaction. An additional, small amplitude geminate recombination was identified at 100 ns. Finally, CO pressure dependent measurements brought out the presence of two transient species in the second order rebinding phase, with time constants ranging from 3 to 100 ms. The available experimental evidence suggests that the two transients are due to the presence of two conformations which do not interconvert within the time frame of the experiment. Computational studies revealed that the plasticity of protein structure is able to define a branched pathway connecting the ligand binding site and the solvent. This allowed to build a kinetic model capable of describing the complete time course of the CO rebinding kinetics to Tf-trHb. Fil: Marcelli, Agnese. European Laboratory for Non-Linear Spectroscopy; Italia Fil: Abbruzzetti, Stefania. Università di Parma; Italia Fil: Bustamante, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Feis, Alessandro. University of Florence; Italia Fil: Bonamore, Alessandra. Università degli studi di Roma "La Sapienza"; Italia Fil: Boffi, Alberto. Università degli studi di Roma "La Sapienza"; Italia Fil: Gellini, Cristina. University of Florence; Italia Fil: Salvi, Pier R.. University of Florence; Italia Fil: Estrin, Dario Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Bruno, Stefano. Università di Parma; Italia Fil: Viappiani, Cristiano. Università di Parma; Italia Fil: Foggi, Paolo. European Laboratory for Non-Linear Spectroscopy; Italia. University of Perugia; Italia
- Subjects :
- Time Factors
lcsh:Medicine
Photochemistry
Molecular Dynamics
Ligands
01 natural sciences
Biochemistry
Biophysics Simulations
Physical Chemistry
purl.org/becyt/ford/1 [https]
Computational Chemistry
FLASH PHOTOLYSIS, TRANSIENT ABSORTION AND OPTOACOUSTIC SPECTROSCOPY
MESH: Ligands
Biomacromolecule-Ligand Interactions
lcsh:Science
HEME-PROTEINS
0303 health sciences
Carbon Monoxide
Multidisciplinary
Hemoproteins
MESH: Kinetics
Chemistry
Ciencias Químicas
Truncated Hemoglobins
VIBRATIONAL-RELAXATION
Ligand (biochemistry)
Femtochemistry
Physicochemical Properties
Reaction Dynamics
Picosecond
Flash photolysis
MYCOBACTERIUM-TUBERCULOSIS
TIME-RESOLVED THERMODYNAMICS
MESH: Carbon Monoxide
CIENCIAS NATURALES Y EXACTAS
Recombination
Research Article
Protein Binding
MESH: Photolysis
PHOTOINDUCED PROCESSES
Absorption spectroscopy
Kinetics
MOLECULAR DYNAMICS SIMULATIONS
Biophysics
010402 general chemistry
CO PHOTODISSOCIATION
03 medical and health sciences
Ultrafast laser spectroscopy
Actinomycetales
purl.org/becyt/ford/1.4 [https]
INTERNAL HYDROPHOBIC CAVITIES
MESH: Protein Binding
THERMOBIFIDA FUSCA TRUNCATED HEMOGLOBIN
Spettroscopia
dinamica di proteine
emoproteine batteriche
assorbimento transiente
laser flash photolysis
dinamica molecolare
fotoacustica
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
CARBON-MONOXIDE
Biology
030304 developmental biology
Photolysis
Otras Ciencias Químicas
Photodissociation
lcsh:R
MESH: Time Factors
Proteins
Computational Biology
0104 chemical sciences
MESH: Actinomycetales
HORSE HEART MYOGLOBIN
Chemical Properties
LIGAND MIGRATION PATHWAYS
MESH: Truncated Hemoglobins
lcsh:Q
PHOTOACOUSTIC CALORIMETRY
TIME-RESOLVED THERMODYNAMICS, INTERNAL HYDROPHOBIC CAVITIES, HORSE HEART MYOGLOBIN, HEME-PROTEINS, MYCOBACTERIUM-TUBERCULOSIS, CARBON-MONOXIDE, PHOTOACOUSTIC CALORIMETRY, VIBRATIONAL-RELAXATION, PHOTOINDUCED PROCESSES, CO PHOTODISSOCIATION
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Database :
- OpenAIRE
- Journal :
- PLoS ONE, PLoS ONE, Public Library of Science, 2012, 7 (7), pp.e39884. ⟨10.1371/journal.pone.0039884⟩, PloS one 7 (2012): e39884–e39884. doi:10.1371/journal.pone.0039884, info:cnr-pdr/source/autori:Marcelli Agnese [ 1 ] ; Abbruzzetti Stefania [ 2 ] ; Bustamante Juan Pablo [ 3 ] ; Feis Alessandro [ 4 ] ; Bonamore Alessandra [ 5 ] ; Boffi Alberto [ 5 ] ; Gellini Cristina [ 4 ] ; Salvi Pier Remigio [ 4 ] ; Estrin Dario A. [ 3 ] ; Bruno Stefano [ 6 ] ; Viappiani Cristiano [ 2 ] ; Foggi Paolo [ 1,7,8 ]/titolo:Following Ligand Migration Pathways from Picoseconds to Milliseconds in Type II Truncated Hemoglobin from Thermobifida fusca/doi:10.1371%2Fjournal.pone.0039884/rivista:PloS one/anno:2012/pagina_da:e39884/pagina_a:e39884/intervallo_pagine:e39884–e39884/volume:7, PLoS ONE, Vol 7, Iss 7, p e39884 (2012), CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET
- Accession number :
- edsair.doi.dedup.....34be98887c69bbf10ec9c02235efc9c1
- Full Text :
- https://doi.org/10.1371/journal.pone.0039884⟩