TY - JOUR
T1 - Steered molecular dynamics analysis of the role of cofilin in increasing the flexibility of actin filaments
AU - Kim, Jae In
AU - Kwon, Junpyo
AU - Baek, Inchul
AU - Na, Sungsoo
N1 - Funding Information:
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (MSIP) (No. 2007-0056094 ) and (No. 2014R1A2A1A11052389 ).
Publisher Copyright:
© 2016 Elsevier B.V.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Cofilin is one of the most essential regulatory proteins and participates in the process of disassembling actin filaments. Cofilin induces conformational changes to actin filaments, and both the bending and torsional rigidity of the filament. In this study, we investigate the effects of cofilin on the mechanical properties of actin filaments using computational methods. Three models defined by their number of bound cofilins are constructed using coarse-grained MARTINI force field, and they are then extended with steered molecular dynamics simulation. After obtaining the stress–strain curves of the models, we calculate their Young's moduli and other mechanical properties that have not yet been determined for actin filaments. We analyze the cause of the different behaviors of the three models based on their atomistic geometrical differences. Finally, it is demonstrated that cofilin binding causes changes in the distances, angles, and stabilities of the residues in actin filaments.
AB - Cofilin is one of the most essential regulatory proteins and participates in the process of disassembling actin filaments. Cofilin induces conformational changes to actin filaments, and both the bending and torsional rigidity of the filament. In this study, we investigate the effects of cofilin on the mechanical properties of actin filaments using computational methods. Three models defined by their number of bound cofilins are constructed using coarse-grained MARTINI force field, and they are then extended with steered molecular dynamics simulation. After obtaining the stress–strain curves of the models, we calculate their Young's moduli and other mechanical properties that have not yet been determined for actin filaments. We analyze the cause of the different behaviors of the three models based on their atomistic geometrical differences. Finally, it is demonstrated that cofilin binding causes changes in the distances, angles, and stabilities of the residues in actin filaments.
KW - Actin
KW - Cofilin
KW - Mechanical property
KW - SMD
UR - http://www.scopus.com/inward/record.url?scp=84984608898&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84984608898&partnerID=8YFLogxK
U2 - 10.1016/j.bpc.2016.08.002
DO - 10.1016/j.bpc.2016.08.002
M3 - Article
C2 - 27589672
AN - SCOPUS:84984608898
SN - 0301-4622
VL - 218
SP - 27
EP - 35
JO - Biophysical Chemistry
JF - Biophysical Chemistry
ER -