Pseudophosphorylation of cardiac myosin regulatory light chain: a promising new tool for treatment of cardiomyopathy

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

Abstract

Many genetic mutations in sarcomeric proteins, including the cardiac myosin regulatory light chain (RLC) encoded by the MYL2 gene, have been implicated in familial cardiomyopathies. Yet, the molecular mechanisms by which these mutant proteins regulate cardiac muscle mechanics in health and disease remain poorly understood. Evidence has been accumulating that RLC phosphorylation has an influential role in striated muscle contraction and, in addition to the conventional modulation via Ca2+ binding to troponin C, it can regulate cardiac muscle function. In this review, we focus on RLC mutations that have been reported to cause cardiomyopathy phenotypes via compromised RLC phosphorylation and elaborate on pseudo-phosphorylation rescue mechanisms. This new methodology has been discussed as an emerging exploratory tool to understand the role of phosphorylation as well as a genetic modality to prevent/rescue cardiomyopathy phenotypes. Finally, we summarize structural effects post-phosphorylation, a phenomenon that leads to an ordered shift in the myosin S1 and RLC conformational equilibrium between two distinct states.

Original languageEnglish (US)
Pages (from-to)57-64
Number of pages8
JournalBiophysical Reviews
Volume9
Issue number1
DOIs
StatePublished - Feb 1 2017

Keywords

  • Cardiomyopathy
  • Hypertrophy
  • Myosin light chains
  • Phosphorylation
  • Pseudo-phosphorylation

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Molecular Biology

Fingerprint Dive into the research topics of 'Pseudophosphorylation of cardiac myosin regulatory light chain: a promising new tool for treatment of cardiomyopathy'. Together they form a unique fingerprint.

Cite this