Characterizing Membrane Association and Periplasmic Transfer of Bacterial Lipoproteins through Molecular Dynamics Simulations

被引:16
|
作者
Rao, Shanlin [1 ]
Bates, George T. [1 ]
Matthews, Callum R. [1 ]
Newport, Thomas D. [1 ]
Vickery, Owen N. [1 ,2 ,3 ]
Stansfeld, Phillip J. [1 ,2 ,3 ]
机构
[1] Univ Oxford, Dept Biochem, South Parks Rd, Oxford OX1 3QU, England
[2] Univ Warwick, Sch Life Sci, Gibbet Hill Campus, Coventry CV4 7AL, W Midlands, England
[3] Univ Warwick, Dept Chem, Gibbet Hill Campus, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
OUTER-MEMBRANE; ESCHERICHIA-COLI; STRUCTURAL BASIS; SIGNAL PEPTIDASE; FORCE-FIELD; PROTEIN; LOLA; LOCALIZATION; BINDING; ENERGY;
D O I
10.1016/j.str.2020.01.012
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
Escherichia coli lipoprotein precursors at the inner membrane undergo three maturation stages before transport by the Lol system to the outer membrane. Here, we develop a pipeline to simulate themembrane association of bacterial lipoproteins in their four maturation states. This has enabled us to model and simulate 81 of the predicted 114 E. coli lipoproteins and reveal their interactions with the host lipid membrane. As part of this set we characterize themembrane contacts of LolB, the lipoprotein involved in periplasmic translocation. We also consider the means and bioenergetics for lipoprotein localization. Our calculations uncover a preference for LolB over LolA and therefore indicate how a lipoprotein may be favorably transferred from the inner to outer membrane. Finally, we reveal that LolC has a role in membrane destabilization, thereby promoting lipoprotein transfer to LolA.
引用
收藏
页码:475 / +
页数:16
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