Myofilament-associated proteins with intrinsic disorder (MAPIDs) play crucial roles in cardiac sarcomere function and can be characterized using state-of-the-art computational modeling techniques.
The cardiac sarcomere is a cellular structure in the heart that enables muscle cells to contract. Dozens of proteins belong to the cardiac sarcomere, which work in tandem to generate force and adapt to demands on cardiac output. Intriguingly, the majority of these proteins have significant intrinsic disorder that contributes to their functions, yet the biophysics of these intrinsically disordered regions (IDRs) have been characterized in limited detail. In this review, we first enumerate these myofilament-associated proteins with intrinsic disorder (MAPIDs) and recent biophysical studies to characterize their IDRs. We secondly summarize the biophysics governing IDR properties and the state-of-the-art in computational tools toward MAPID identification and characterization of their conformation ensembles. We conclude with an overview of future computational approaches toward broadening the understanding of intrinsic disorder in the cardiac sarcomere.
Sun et al. (Sun,) conducted a review in Cardiomyopathy and myofilament function. Myofilament-associated proteins with intrinsic disorder (MAPIDs) play crucial roles in cardiac sarcomere function and can be characterized using state-of-the-art computational modeling techniques.