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iMAX FRET (Information Maximized FRET) for Multipoint Single-Molecule Structural Analysis

Title
iMAX FRET (Information Maximized FRET) for Multipoint Single-Molecule Structural Analysis
Authors
JoshiBhagyashree S.de LannoyCarlosHowarthMark R.KimSung HyunJooChirlmin
Ewha Authors
주철민
SCOPUS Author ID
주철민scopus
Issue Date
2024
Journal Title
Nano Letters
ISSN
1530-6984JCR Link
Citation
Nano Letters vol. 24, no. 28, pp. 8487 - 8494
Keywords
computational structure predictionprogrammable DNA bindingsingle-molecule conformational analysissingle-molecule FRETsingle-molecule structural analysis
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Understanding the structure of biomolecules is vital for deciphering their roles in biological systems. Single-molecule techniques have emerged as alternatives to conventional ensemble structure analysis methods for uncovering new biology in molecular dynamics and interaction studies, yet only limited structural information could be obtained experimentally. Here, we address this challenge by introducing iMAX FRET, a one-pot method that allows ab initio 3D profiling of individual molecules using two-color FRET measurements. Through the stochastic exchange of fluorescent weak binders, iMAX FRET simultaneously assesses multiple distances on a biomolecule within a few minutes, which can then be used to reconstruct the coordinates of up to four points in each molecule, allowing structure-based inference. We demonstrate the 3D reconstruction of DNA nanostructures, protein quaternary structures, and conformational changes in proteins. With iMAX FRET, we provide a powerful approach to advance the understanding of biomolecular structure by expanding conventional FRET analysis to three dimensions. © 2024 The Authors. Published by American Chemical Society.
DOI
10.1021/acs.nanolett.4c00447
Appears in Collections:
자연과학대학 > 물리학전공 > Journal papers
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