TY - JOUR
T1 - iMAX FRET (Information Maximized FRET) for Multipoint Single-Molecule Structural Analysis
AU - Joshi, Bhagyashree S.
AU - de Lannoy, Carlos
AU - Howarth, Mark R.
AU - Kim, Sung Hyun
AU - Joo, Chirlmin
PY - 2024
Y1 - 2024
N2 - 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.
AB - 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.
KW - computational structure prediction
KW - programmable DNA binding
KW - single-molecule conformational analysis
KW - single-molecule FRET
KW - single-molecule structural analysis
UR - http://www.scopus.com/inward/record.url?scp=85198077034&partnerID=8YFLogxK
U2 - 10.1021/acs.nanolett.4c00447
DO - 10.1021/acs.nanolett.4c00447
M3 - Article
AN - SCOPUS:85198077034
SN - 1530-6984
VL - 24
SP - 8487
EP - 8494
JO - Nano Letters
JF - Nano Letters
IS - 28
ER -