Label-free detection and profiling of individual solution-phase molecules

• 成果类型: Article
• 署名作者: Needham, Lisa-Maria; Saavedra, Carlos; Rasch, Julia K.; Sole-Barber, Daniel; Schweitzer, Beau S.; Fairhall, Alex J.; Vollbrecht, Cecilia H.; Wan, Sushu; Podorova, Yulia; Bergsten, Anders J.; Mehlenbacher, Brandon; Zhang, Zhao; Tenbrake, Lukas; Saimi, Jovanna; Kneely, Lucy C.; Kirkwood, Jackson S.; Pfeifer, Hannes; Chapman, Edwin R.; Goldsmith, Randall H.
• 署名单位: University of Wisconsin System; University of Wisconsin Madison; University of Cambridge; Howard Hughes Medical Institute; University of Wisconsin System; University of Wisconsin Madison; University of Wisconsin System; University of Wisconsin Madison; University of Bonn; University of Cambridge; Kalamazoo College
• 刊物名称: Nature
• ISSN/ISSBN: 0028-6606
• DOI: 10.1038/s41586-024-07370-8
• 发表日期: 2024-05-30
• 关键词: carbonic-anhydrase; optical-detection; single; spectroscopy; absorption; dls

摘要

Most chemistry and biology occurs in solution, in which conformational dynamics and complexation underlie behaviour and function. Single-molecule techniques(1) are uniquely suited to resolving molecular diversity and new label-free approaches are reshaping the power of single-molecule measurements. A label-free single-molecule method(2-16) capable of revealing details of molecular conformation in solution(17,18) would allow a new microscopic perspective of unprecedented detail. Here we use the enhanced light-molecule interactions in high-finesse fibre-based Fabry-P & eacute;rot microcavities(19-21) to detect individual biomolecules as small as 1.2 kDa, a ten-amino-acid peptide, with signal-to-noise ratios (SNRs) >100, even as the molecules are unlabelled and freely diffusing in solution. Our method delivers 2D intensity and temporal profiles, enabling the distinction of subpopulations in mixed samples. Notably, we observe a linear relationship between passage time and molecular radius, unlocking the potential to gather crucial information about diffusion and solution-phase conformation. Furthermore, mixtures of biomolecule isomers of the same molecular weight and composition but different conformation can also be resolved. Detection is based on the creation of a new molecular velocity filter window and a dynamic thermal priming mechanism that make use of the interplay between optical and thermal dynamics(22,23) and Pound-Drever-Hall (PDH) cavity locking(24) to reveal molecular motion even while suppressing environmental noise. New in vitro ways of revealing molecular conformation, diversity and dynamics can find broad potential for applications in the life and chemical sciences.