费斯特共振能量转移
生物分子
荧光团
脂质体
膜
化学
单分子微动
分子
生物物理学
脂质双层
荧光
生物膜
纳米技术
生物化学
材料科学
生物
量子力学
物理
有机化学
作者
Dongfei Ma,Chunhua Xu,Wenqing Hou,Chunyu Zhao,Jianbing Ma,Xing‐Yuan Huang,Qi Jia,Lu Ma,Jiajie Diao,Cong Liu,Ming Li,Ying Lü
标识
DOI:10.1002/anie.201813888
摘要
Abstract Tracking membrane‐interacting molecules and visualizing their conformational dynamics are key to understanding their functions. It is, however, challenging to accurately probe the positions of a molecule relative to a membrane. Herein, a single‐molecule method, termed LipoFRET, is reported to assess interplay between molecules and liposomes. It takes advantage of FRET between a single fluorophore attached to a biomolecule and many quenchers in a liposome. This method was used to characterize interactions between α‐synuclein (α‐syn) and membranes. These results revealed that the N‐terminus of α‐syn inserts into the membrane and spontaneously transitions between different depths. In contrast, the C‐terminal tail of α‐syn is regulated by calcium ions and floats in solution in two conformations. LipoFRET is a powerful tool to investigate membrane‐interacting biomolecules with sub‐nanometer precision at the single‐molecule level.
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