膜
生物分子
化学
费斯特共振能量转移
生物物理学
胞浆
跨膜蛋白
细胞外
等离子体
生物化学
生物
荧光
酶
量子力学
物理
受体
作者
Wenqing Hou,Dongfei Ma,Xiaolong He,Weijing Han,Jianbing Ma,Hao Wang,Chunhua Xu,Ruipei Xie,Qihui Fan,Fangfu Ye,Shuxin Hu,Ming Li,Ying Lü
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-12-05
卷期号:21 (1): 485-491
被引量:9
标识
DOI:10.1021/acs.nanolett.0c03941
摘要
Characterization of biomolecular dynamics at cellular membranes lags far behind that in solutions because of challenges to measure transmembrane trafficking with subnanometer precision. Herein, by introducing nonfluorescent quenchers into extracellular environment of live cells, we adopted Förster resonance energy transfer from one donor to multiple quenchers to measure positional changes of biomolecules in plasma membranes. We demonstrated the method by monitoring flip-flops of individual lipids and by capturing transient states of the host defense peptide LL-37 in plasma membranes. The method was also applied to investigate the interaction of the necroptosis-associated protein MLKL with plasma membranes, showing a few distinct depths of MLKL insertion. Our method is especially powerful to quantitate the dynamics of proteins at the cytosolic leaflets of plasma membranes which are usually not accessible by conventional techniques. The method will find wide applications in the systematic analysis of fundamental cellular processes at plasma membranes.
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