费斯特共振能量转移
单分子微动
生物分子
DNA
荧光团
化学
纳米技术
生物物理学
荧光
材料科学
物理
生物
生物化学
光学
作者
Mike Filius,Sung Wan Kim,Ivo Severins,Chirlmin Joo
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-03-19
卷期号:21 (7): 3295-3301
被引量:14
标识
DOI:10.1021/acs.nanolett.1c00725
摘要
Single-molecule FRET is a versatile tool to study nucleic acids and proteins at the nanometer scale. However, currently, only a couple of FRET pairs can be reliably measured on a single object, which makes it difficult to apply single-molecule FRET for structural analysis of biomolecules. Here, we present an approach that allows for the determination of multiple distances between FRET pairs in a single object. We use programmable, transient binding between short DNA strands to resolve the FRET efficiency of multiple fluorophore pairs. By allowing only a single FRET pair to be formed at a time, we can determine the pair distance with subnanometer precision. The distance between other pairs are determined by sequentially exchanging DNA strands. We name this multiplexing approach FRET X for FRET via DNA eXchange. Our FRET X technology will be a tool for the high-resolution analysis of biomolecules and nanostructures.
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