Molecular modeling of disease causing mutations in domain C1 of cMyBP-C.
PLoS One
; 8(3): e59206, 2013.
Article
em En
| MEDLINE
| ID: mdl-23527136
ABSTRACT
Cardiac myosin binding protein-C (cMyBP-C) is a multi-domain (C0-C10) protein that regulates heart muscle contraction through interaction with myosin, actin and other sarcomeric proteins. Several mutations of this protein cause familial hypertrophic cardiomyopathy (HCM). Domain C1 of cMyBP-C plays a central role in protein interactions with actin and myosin. Here, we studied structure-function relationship of three disease causing mutations, Arg177His, Ala216Thr and Glu258Lys of the domain C1 using computational biology techniques with its available X-ray crystal structure. The results suggest that each mutation could affect structural properties of the domain C1, and hence it's structural integrity through modifying intra-molecular arrangements in a distinct mode. The mutations also change surface charge distributions, which could impact the binding of C1 with other sarcomeric proteins thereby affecting contractile function. These structural consequences of the C1 mutants could be valuable to understand the molecular mechanisms for the disease.
Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Proteínas de Transporte
/
Modelos Moleculares
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Estrutura Terciária de Proteína
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Mutação de Sentido Incorreto
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Cardiomiopatia Hipertrófica Familiar
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article