Efficient and reversible chirality induction between protein and achiral plasmonic assemblies

Chiral molecules in nature usually show optical activity only in the deep ultraviolet, whereas artificial chiral plasmonic nanostructures can generate much stronger responses at visible and near-infrared wavelengths. An important challenge is whether the abundant biomolecular chirality in nature can be directly transferred to achiral plasmonic systems without elaborate three-dimensional nanofabrication. Here we show that the mechanical stretching of protein molecules anchored within achiral gold nanoparticle assemblies strongly enhances and reversibly modulates plasmon-coupled circular dichroism. Stretching amplifies the chiroptical response to an ellipticity of 1.18° and a dissymmetry factor of 0.2, far exceeding conventional hotspot-based strategies. Repeated stretching and relaxation further enable reversible switching over more than 100 cycles. Simulations and in situ spectroscopy indicate that the deformation of protein changes its conformation and dipole alignment, thereby strengthening the plasmonic chiral response. These findings establish a route to achieve dynamically controllable chiroptical activity in achiral plasmonic assemblies, revealing how small biomolecular deformations can strongly influence plasmonic responses of much larger nanostructures.

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Journal
Nature Materials
Published
2026-04-15
DOI
https://doi.org/10.1038/s41563-026-02586-7
Primary Topic
Metamaterials and Metasurfaces Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Efficient and reversible chirality induction between protein and achiral plasmonic assemblies

Franziska Lissel, Tobias A. F. König, Patrick T. Probst, Martin Müller et al.
Nature Materials
Metamaterials and Metasurfaces Applications
article

Efficient and reversible chirality induction between protein and achiral plasmonic assemblies

Franziska Lissel, Tobias A. F. König, Patrick T. Probst, Martin Müller, Bo Yin, Ziwei Zhou, Holger Merlitz, Artur Movsesyan, Yaroslava G. Yingling, Alexander O. Govorov, Nicolás Pazos‐Pérez, Anja Maria Steiner, Andreas Fery, Nina Tverdokhleb, Ramón A. Álvarez‐Puebla, Nicholas A. Kotov, Zhiming M. Wang, Vaibhav Gupta, Olga Guskova, Mirjam Taube
article en

Abstract

Chiral molecules in nature usually show optical activity only in the deep ultraviolet, whereas artificial chiral plasmonic nanostructures can generate much stronger responses at visible and near-infrared wavelengths. An important challenge is whether the abundant biomolecular chirality in nature can be directly transferred to achiral plasmonic systems without elaborate three-dimensional nanofabrication. Here we show that the mechanical stretching of protein molecules anchored within achiral gold nanoparticle assemblies strongly enhances and reversibly modulates plasmon-coupled circular dichroism. Stretching amplifies the chiroptical response to an ellipticity of 1.18° and a dissymmetry factor of 0.2, far exceeding conventional hotspot-based strategies. Repeated stretching and relaxation further enable reversible switching over more than 100 cycles. Simulations and in situ spectroscopy indicate that the deformation of protein changes its conformation and dipole alignment, thereby strengthening the plasmonic chiral response. These findings establish a route to achieve dynamically controllable chiroptical activity in achiral plasmonic assemblies, revealing how small biomolecular deformations can strongly influence plasmonic responses of much larger nanostructures.

Nature Materials
Institució Catalana de Recerca i Estudis Avançats (ES), Centre National de la Recherche Scientifique (FR), Synopsys (Switzerland) (CH), North Carolina State University (US), University of Electronic Science and Technology of China (CN), Universität Hamburg (DE), Aix-Marseille Université (FR), University of Michigan (US), Synopsys (United States) (US), Ohio University (US), Leibniz Institute of Polymer Research (DE), BioSurfaces (United States) (US), Universitat Rovira i Virgili (ES), Kobe University (JP), Technische Universität Dresden (DE), Hamburg University of Technology (DE)
National Science Foundation, Alexander von Humboldt-Stiftung, Banco Santander, Deutsche Forschungsgemeinschaft, Volkswagen Foundation, United States-Israel Binational Science Foundation, Bundesministerium für Bildung und Forschung, Technische Universität Dresden, Universitat Rovira i Virgili, Leibniz-Institut für Polymerforschung Dresden, Engineering and Physical Sciences Research Council, Leibniz-Gemeinschaft, Elitenetzwerk Bayern, Division of Chemical, Bioengineering, Environmental, and Transport Systems, HORIZON EUROPE European Innovation Council
Openalex Percentile: Top 25%
Metamaterials and Metasurfaces Applications
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