Publication

Light-Responsive Polymer Particles as Force Clamps for the Mechanical Unfolding of Target Molecules

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Last modified
  • 05/15/2025
Type of Material
Authors
    Hanquan Su, Emory UniversityZheng Liu, Emory UniversityYang Liu, Emory UniversityVictor Pui-Yan Ma, Emory UniversityAaron Blanchard, Georgia Institute of TechnologyJing Zhao, Emory UniversityKornelia Galior, Emory UniversityRichard Dyer, Emory UniversityKhalid Salaita, Emory University
Language
  • English
Date
  • 2018-04-01
Publisher
  • American Chemical Society
Publication Version
Copyright Statement
  • © 2018 American Chemical Society.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1530-6984
Volume
  • 18
Issue
  • 4
Start Page
  • 2630
End Page
  • 2636
Grant/Funding Information
  • The work was supported by grants from the NSF CAREER Award (1350829); the DARPA BTO (HR0011-16-2-0011) and the NIH (R01-GM097399).
  • V.P.-Y.M. is supported by the National Cancer Institute Predoctoral to Postdoctoral Fellow Transition Award (F99CA223074).
  • A.T.B. is supported by the NSF Graduate Research Fellowship Program (1444932).
  • This project was supported in part by the Robert P. Apkarian Integrated Electron Microscopy Core.
Supplemental Material (URL)
Abstract
  • Single-molecule force spectroscopy techniques are powerful tools for investigating the mechanical unfolding of biomolecules. However, they are limited in throughput and require dedicated instrumentation. Here, we report a force-generating particle that can unfold target molecules on-demand. The particle consists of a plasmonic nanorod core encapsulated with a thermoresponsive polymer shell. Optical heating of the nanorod leads to rapid collapse of the polymer, thus transducing light into mechanical work to unfold target molecules. The illumination tunes the duration and degree of particle collapse, thus controlling the lifetime and magnitude of applied forces. Single-molecule fluorescence imaging showed reproducible mechanical unfolding of DNA hairpins. We also demonstrate the triggering of 50 different particles in <1 min, exceeding the speed of conventional atomic force microscopy. The polymer force clamp represents a facile and bottom-up approach to force manipulation.
Author Notes
Keywords
Research Categories
  • Chemistry, General
  • Engineering, Biomedical

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