scholarly journals Biophysics of filament length regulation by molecular motors

2013 ◽  
Vol 10 (3) ◽  
pp. 036004 ◽  
Author(s):  
Hui-Shun Kuan ◽  
M D Betterton
2014 ◽  
Vol 4 (6) ◽  
pp. 20140031 ◽  
Author(s):  
Louis Reese ◽  
Anna Melbinger ◽  
Erwin Frey

The cytoskeleton is regulated by a plethora of enzymes that influence the stability and dynamics of cytoskeletal filaments. How microtubules (MTs) are controlled is of particular importance for mitosis, during which dynamic MTs are responsible for proper segregation of chromosomes. Molecular motors of the kinesin-8 protein family have been shown to depolymerize MTs in a length-dependent manner, and recent experimental and theoretical evidence suggests a possible role for kinesin-8 in the dynamic regulation of MTs. However, so far the detailed molecular mechanisms of how these molecular motors interact with the growing MT tip remain elusive. Here we show that two distinct scenarios for the interactions of kinesin-8 with the MT tip lead to qualitatively different MT dynamics, including accurate length control as well as intermittent dynamics. We give a comprehensive analysis of the regimes where length regulation is possible and characterize how the stationary length depends on the biochemical rates and the bulk concentrations of the various proteins. For a neutral scenario, where MTs grow irrespective of whether the MT tip is occupied by a molecular motor, length regulation is possible only for a narrow range of biochemical rates, and, in particular, limited to small polymerization rates. By contrast, for an inhibition scenario, where the presence of a motor at the MT tip inhibits MT growth, the regime where length regulation is possible is extremely broad and includes high growth rates. These results also apply to situations where a polymerizing enzyme like XMAP215 and kinesin-8 mutually exclude each other from the MT tip. Moreover, we characterize the differences in the stochastic length dynamics between the two scenarios. While for the neutral scenario length is tightly controlled, length dynamics is intermittent for the inhibition scenario and exhibits extended periods of MT growth and shrinkage. On a broader perspective, the set of models established in this work quite generally suggest that mutual exclusion of molecules at the ends of cytoskeletal filaments is an important factor for filament dynamics and regulation.


2019 ◽  
Vol 116 (3) ◽  
pp. 551a
Author(s):  
Balazs Kiss ◽  
Paola Tonino ◽  
Justin Kolb ◽  
John E. Smith ◽  
Henk L. Granzier

2012 ◽  
Vol 108 (25) ◽  
Author(s):  
Anna Melbinger ◽  
Louis Reese ◽  
Erwin Frey

2012 ◽  
Vol 108 (25) ◽  
Author(s):  
Denis Johann ◽  
Christoph Erlenkämper ◽  
Karsten Kruse

2020 ◽  
Vol 6 (46) ◽  
pp. eabc1992
Author(s):  
Balázs Kiss ◽  
Jochen Gohlke ◽  
Paola Tonino ◽  
Zaynab Hourani ◽  
Justin Kolb ◽  
...  

Regulating the thin-filament length in muscle is crucial for controlling the number of myosin motors that generate power. The giant protein nebulin forms a long slender filament that associates along the length of the thin filament in skeletal muscle with functions that remain largely obscure. Here nebulin’s role in thin-filament length regulation was investigated by targeting entire super-repeats in the Neb gene; nebulin was either shortened or lengthened by 115 nm. Its effect on thin-filament length was studied using high-resolution structural and functional techniques. Results revealed that thin-filament length is strictly regulated by the length of nebulin in fast muscles. Nebulin’s control is less tight in slow muscle types where a distal nebulin-free thin-filament segment exists, the length of which was found to be regulated by leiomodin-2 (Lmod2). We propose that strict length control by nebulin promotes high-speed shortening and that dual-regulation by nebulin/Lmod2 enhances contraction efficiency.


2005 ◽  
Vol 45 (supplement) ◽  
pp. S160
Author(s):  
S. Ohmori ◽  
J. Utaka ◽  
S. Kurihara ◽  
S. Ishiwata ◽  
N. Fukuda

2016 ◽  
Vol 11 (03) ◽  
pp. 117-126 ◽  
Author(s):  
Peter R. Greene

The transverse thermal fluctuations of the myosin molecule are significant. This paper explores the contribution of lateral myosin bending to the developed crossbridge force and power stroke. The equipartition theorem is used to calculate the mode amplitudes for myosin bending. Crossbridge axial force [Formula: see text] and power stroke [Formula: see text] are developed by transverse in-plane fluctuations along the [Formula: see text]- and [Formula: see text]-axes. Practical applications include the effects of temperature on the flexibility of the myosin molecule stiffness and tension, relevant to man-made fabrication of synthetic muscle using micromachines and nanowires. Scaling laws for the [Formula: see text] bending amplitude depend on filament length, mode number, and stiffness, as [Formula: see text], and (EI)[Formula: see text]. This paper quantifies the effects of thermal motion on the mechanics of miniature molecular motors, including the muscle crossbridge.


Sign in / Sign up

Export Citation Format

Share Document