Effect of Cholesterol on C99 Dimerization: Revealed by Molecular Dynamics Simulations

被引:4
作者
Li, Cheng-Dong [1 ]
Junaid, Muhammad [1 ]
Shan, Xiaoqi [1 ]
Wang, Yanjing [1 ]
Wang, Xiangeng [1 ]
Khan, Abbas [1 ]
Wei, Dong-Qing [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Dept Bioinformat & Biol Stat, State Key Lab Microbial Metab,Joint Lab Int Cooper, Shanghai, Peoples R China
[2] Peng Cheng Lab, Shenzhen, Peoples R China
基金
美国国家科学基金会;
关键词
cholesterol; C99; dimerization; molecular dynamics simulations; Alzheimer's disease; AMYLOID PRECURSOR PROTEIN; TRANSMEMBRANE DOMAIN; ALZHEIMERS-DISEASE; GAMMA-SECRETASE; FORCE-FIELD; A-BETA; MODEL; BINDING; CLEAVAGE; DIMER;
D O I
10.3389/fmolb.2022.872385
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
C99 is the immediate precursor for amyloid beta (A beta) and therefore is a central intermediate in the pathway that is believed to result in Alzheimer's disease (AD). It has been suggested that cholesterol is associated with C99, but the dynamic details of how cholesterol affects C99 assembly and the A beta formation remain unclear. To investigate this question, we employed coarse-grained and all-atom molecular dynamics simulations to study the effect of cholesterol and membrane composition on C99 dimerization. We found that although the existence of cholesterol delays C99 dimerization, there is no direct competition between C99 dimerization and cholesterol association. In contrast, the existence of cholesterol makes the C99 dimer more stable, which presents a cholesterol binding C99 dimer model. Cholesterol and membrane composition change the dimerization rate and conformation distribution of C99, which will subsequently influence the production of A beta. Our results provide insights into the potential influence of the physiological environment on the C99 dimerization, which will help us understand A beta formation and AD's etiology.
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页数:10
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