Structures of the troponin core domain containing the cardiomyopathy-causing mutants studied by small-angle X-ray scattering.

ABSTRACT: Troponin (Tn), consisting of three subunits, TnC, TnI, and TnT, is a protein in the thin filaments in muscle, and, together with another thin-filament protein tropomyosin (Tm), plays a major role in regulation of muscle contraction. Various mutations of Tn cause familial hypertrophic cardiomyopathy. These mutations are directly related to aberrations in this regulatory mechanism. Here we focus on the mutations E244D and K247R of TnT, which reside in the middle of the pathway of the Ca(2+)-binding signal from TnC to Tm. These mutations induce an increase in the maximum tension of cardiac muscle without changes in Ca(2+)-sensitivity. As a first step toward elucidating the molecular mechanism underlying this functional aberration, we carried out small-angle X-ray scattering experiments on the

SUBMITTER: Matsuo T 

PROVIDER: S-EPMC4736830 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature