Recapitulation of cell-like KRAS4b membrane dynamics on complex biomimetic membranes

被引:6
作者
Shrestha, Rebika [1 ]
Chen, De [1 ]
Frank, Peter [1 ]
Nissley, Dwight V. [1 ]
Turbyville, Thomas J. [1 ]
机构
[1] NCI, RAS Initiat, Canc Res Technol Program, Frederick Natl Lab Canc Res,Leidos Biomed Res Inc, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
RAS FORMS DIMERS; PLASMA-MEMBRANE; LIPID-BILAYERS; H-RAS; PROTEIN; DIFFUSION; ACTIVATION; SURFACES; DOMAINS;
D O I
10.1016/j.isci.2021.103608
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding the spatiotemporal distribution and dynamics of RAS on the plasma membrane (PM) is the key for elucidating the molecular mechanisms of the RAS signaling pathway. Single particle tracking (SPT) experiments show that in cells, KRAS diffuses in at least three interchanging states on the cellular PM; however, KRAS remains monomeric and always shows homogeneous diffusion on artificial membranes. Here, we show for the first time on a supported lipid bilayer composed of heterogeneous lipid components that we can recapitulate the three-state diffusion of KRAS seen in cells. The use of a biologically relevant eight-lipid system opens a new frontier in the biophysical studies of RAS and other membrane associated proteins on a biomimetic system that recapitulates the complexity of a cellular PM.
引用
收藏
页数:17
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