| Literature DB >> 29353351 |
Abstract
Titin is a filamentous protein spanning the half-sarcomere, with spring-like properties in the I-band region. Various structural, signaling, and mechanical functions have been associated with titin, but not all of these are fully elucidated and accepted in the scientific community. Here, I discuss the primary mechanical functions of titin, including its accepted role in passive force production, stabilization of half-sarcomeres and sarcomeres, and its controversial contribution to residual force enhancement, passive force enhancement, energetics, and work production in shortening muscle. Finally, I provide evidence that titin is a molecular spring whose stiffness changes with muscle activation and actin-myosin-based force production, suggesting a novel model of force production that, aside from actin and myosin, includes titin as a "third contractile" filament. Using this three-filament model of sarcomeres, the stability of (half-) sarcomeres, passive force enhancement, residual force enhancement, and the decrease in metabolic energy during and following eccentric contractions can be explained readily.Entities:
Keywords: Active/passive force regulation; Cross-bridge theory; Force production; Mechanical functions; Mechanisms of muscle contraction; Molecular spring; Muscle energetics; Muscle shortening; Three filament sarcomere model; Titin
Year: 2018 PMID: 29353351 PMCID: PMC6082311 DOI: 10.1007/s12551-017-0395-y
Source DB: PubMed Journal: Biophys Rev ISSN: 1867-2450