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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.

Original publication

DOI

10.1021/acs.nanolett.4c00447

Type

Journal article

Journal

Nano Lett

Publication Date

17/07/2024

Volume

24

Pages

8487 - 8494

Keywords

computational structure prediction, programmable DNA binding, single-molecule FRET, single-molecule conformational analysis, single-molecule structural analysis, Fluorescence Resonance Energy Transfer, DNA, Single Molecule Imaging, Nanostructures, Proteins, Molecular Dynamics Simulation