A quantitative model for oxygen uptake and release in a family of hemeproteins

Motivation: Hemeproteins have many diverse functions that largely depend on the rate at which they uptake or release small ligands, like oxygen. These proteins have been extensively studied using either simulations or experiments, albeit only qualitatively and one or two proteins at a time. Results:...

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Detalhes bibliográficos
Autores: Bustamante, Juan Pablo, Szretter Noste, María Eugenia, Sued, Raquel Mariela, Marti, Marcelo Adrian, Estrin, Dario Ariel, Boechi, Leonardo
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/55125
Acesso em linha:http://hdl.handle.net/11336/55125
Access Level:acceso abierto
Palavra-chave:Hemeproteins
Uptake And Release Oxygen
Truncated Hemoglobins
Association And Dissociation Kinetic Rate Constants
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
id AR_ec323dc0e91cbfd594f320f71bfc84bd
oai_identifier_str oai:ri.conicet.gov.ar:11336/55125
network_acronym_str AR
network_name_str Argentina
repository_id_str
dc.title.none.fl_str_mv A quantitative model for oxygen uptake and release in a family of hemeproteins
title A quantitative model for oxygen uptake and release in a family of hemeproteins
spellingShingle A quantitative model for oxygen uptake and release in a family of hemeproteins
Bustamante, Juan Pablo
Hemeproteins
Uptake And Release Oxygen
Truncated Hemoglobins
Association And Dissociation Kinetic Rate Constants
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
title_short A quantitative model for oxygen uptake and release in a family of hemeproteins
title_full A quantitative model for oxygen uptake and release in a family of hemeproteins
title_fullStr A quantitative model for oxygen uptake and release in a family of hemeproteins
title_full_unstemmed A quantitative model for oxygen uptake and release in a family of hemeproteins
title_sort A quantitative model for oxygen uptake and release in a family of hemeproteins
dc.creator.none.fl_str_mv Bustamante, Juan Pablo
Szretter Noste, María Eugenia
Sued, Raquel Mariela
Marti, Marcelo Adrian
Estrin, Dario Ariel
Boechi, Leonardo
author Bustamante, Juan Pablo
author_facet Bustamante, Juan Pablo
Szretter Noste, María Eugenia
Sued, Raquel Mariela
Marti, Marcelo Adrian
Estrin, Dario Ariel
Boechi, Leonardo
author_role author
author2 Szretter Noste, María Eugenia
Sued, Raquel Mariela
Marti, Marcelo Adrian
Estrin, Dario Ariel
Boechi, Leonardo
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Hemeproteins
Uptake And Release Oxygen
Truncated Hemoglobins
Association And Dissociation Kinetic Rate Constants
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
topic Hemeproteins
Uptake And Release Oxygen
Truncated Hemoglobins
Association And Dissociation Kinetic Rate Constants
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
description Motivation: Hemeproteins have many diverse functions that largely depend on the rate at which they uptake or release small ligands, like oxygen. These proteins have been extensively studied using either simulations or experiments, albeit only qualitatively and one or two proteins at a time. Results: We present a physical-chemical model, which uses data obtained exclusively from computer simulations, to describe the uptake and release of oxygen in a family of hemeproteins, called truncated hemoglobins (trHbs). Through a rigorous statistical analysis we demonstrate that our model successfully recaptures all the reported experimental oxygen association and dissociation kinetic rate constants, thus allowing us to establish the key factors that determine the rates at which these hemeproteins uptake and release oxygen. We found that internal tunnels as well as the distal site water molecules control ligand uptake, whereas oxygen stabilization by distal site residues controls ligand release. Because these rates largely determine the functions of these hemeproteins, these approaches will also be important tools in characterizing the trHbs members with unknown functions.
publishDate 2016
dc.date.none.fl_str_mv 2016-06
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/55125
Bustamante, Juan Pablo; Szretter Noste, María Eugenia; Sued, Raquel Mariela; Marti, Marcelo Adrian; Estrin, Dario Ariel; et al.; A quantitative model for oxygen uptake and release in a family of hemeproteins; Oxford University Press; Bioinformatics (Oxford, England); 32; 12; 6-2016; 1805-1813
1367-4803
CONICET Digital
CONICET
url http://hdl.handle.net/11336/55125
identifier_str_mv Bustamante, Juan Pablo; Szretter Noste, María Eugenia; Sued, Raquel Mariela; Marti, Marcelo Adrian; Estrin, Dario Ariel; et al.; A quantitative model for oxygen uptake and release in a family of hemeproteins; Oxford University Press; Bioinformatics (Oxford, England); 32; 12; 6-2016; 1805-1813
1367-4803
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1093/bioinformatics/btw083
info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/bioinformatics/article/32/12/1805/1744225
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Oxford University Press
publisher.none.fl_str_mv Oxford University Press
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1799194986302930944
spelling A quantitative model for oxygen uptake and release in a family of hemeproteinsBustamante, Juan PabloSzretter Noste, María EugeniaSued, Raquel MarielaMarti, Marcelo AdrianEstrin, Dario ArielBoechi, LeonardoHemeproteinsUptake And Release OxygenTruncated HemoglobinsAssociation And Dissociation Kinetic Rate Constantshttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Motivation: Hemeproteins have many diverse functions that largely depend on the rate at which they uptake or release small ligands, like oxygen. These proteins have been extensively studied using either simulations or experiments, albeit only qualitatively and one or two proteins at a time. Results: We present a physical-chemical model, which uses data obtained exclusively from computer simulations, to describe the uptake and release of oxygen in a family of hemeproteins, called truncated hemoglobins (trHbs). Through a rigorous statistical analysis we demonstrate that our model successfully recaptures all the reported experimental oxygen association and dissociation kinetic rate constants, thus allowing us to establish the key factors that determine the rates at which these hemeproteins uptake and release oxygen. We found that internal tunnels as well as the distal site water molecules control ligand uptake, whereas oxygen stabilization by distal site residues controls ligand release. Because these rates largely determine the functions of these hemeproteins, these approaches will also be important tools in characterizing the trHbs members with unknown functions.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; ArgentinaFil: Szretter Noste, María Eugenia. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Sued, Raquel Mariela. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Marti, Marcelo Adrian. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales; ArgentinaFil: 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; ArgentinaFil: Boechi, Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; ArgentinaOxford University Press2016-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/55125Bustamante, Juan Pablo; Szretter Noste, María Eugenia; Sued, Raquel Mariela; Marti, Marcelo Adrian; Estrin, Dario Ariel; et al.; A quantitative model for oxygen uptake and release in a family of hemeproteins; Oxford University Press; Bioinformatics (Oxford, England); 32; 12; 6-2016; 1805-18131367-4803CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1093/bioinformatics/btw083info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/bioinformatics/article/32/12/1805/1744225info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2024-05-08T13:40:35Zoai:ri.conicet.gov.ar:11336/55125instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982024-05-08 13:40:35.78CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
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