Myomerger Induces Membrane Hemifusion and Regulates Fusion Pore Expansion

被引:0
|
作者
Di Bartolo, Ary Lautaro [1 ]
Caparotta, Marcelo [2 ]
Polo, Luis Mariano [3 ]
Masone, Diego [3 ,4 ]
机构
[1] Univ Nacl Cuyo UNCuyo, Fac Ciencias Exactas & Nat, RA-5500 Mendoza, Argentina
[2] Univ Florida, Dept Chem, Quantum Theory Project, Gainesville, FL 32611 USA
[3] Univ Nacl Cuyo, Consejo Nacl Invest Cient & Tecn CONICET, Inst Histol & Embriol Mendoza IHEM, RA-5500 Mendoza, Argentina
[4] Univ Nacl Cuyo, Fac Ingn, RA-5500 Mendoza, Argentina
关键词
INFLUENZA-VIRUS HEMAGGLUTININ; MOLECULAR-DYNAMICS METHOD; FREE-ENERGY LANDSCAPE; REACTION COORDINATE; ALPHA-SYNUCLEIN; FORCE-FIELD; SIMULATIONS; CHARMM; STALK; GUI;
D O I
10.1021/acs.biochem.3c00682
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane fusion is a crucial mechanism in a wide variety of important events in cell biology from viral infection to exocytosis. However, despite many efforts and much progress, cell-cell fusion has remained elusive to our understanding. Along the life of the fusion pore, large conformational changes take place from the initial lipid bilayer bending, passing through the hemifusion intermediates, and ending with the formation of the first nascent fusion pore. In this sense, computer simulations are an ideal technique for describing such complex lipid remodeling at the molecular level. In this work, we studied the role played by the muscle-specific membrane protein Myomerger during the formation of the fusion pore. We have conducted mu s length atomistic and coarse-grained molecular dynamics, together with free-energy calculations using ad hoc collective variables. Our results show that Myomerger favors the hemifusion diaphragm-stalk transition, reduces the nucleation-expansion energy difference, and promotes the formation of nonenlarging fusion pores.
引用
收藏
页码:815 / 826
页数:12
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