Plasmonic Enhancement of Fluorescence and Protein Dynamics in Living Mammalian Cells

Journal Article (2026)
Author(s)

Marco Locarno (TU Delft - ImPhys/Brinks group)

Qiangrui Dong (TU Delft - ImPhys/Brinks group)

Marco Post (TU Delft - ImPhys/Brinks group)

Xin Meng (TU Delft - ImPhys/Brinks group)

Cristiano Glessi (TU Delft - ImPhys/Hagen group)

Nynke Marije Hettema (TU Delft - BN/Liedewij Laan Lab)

Nidas Brandsma (Student TU Delft)

Alejandro Castañeda Garcia (TU Delft - Pattern Recognition and Bioinformatics)

Srividya Ganapathy (TU Delft - ImPhys/Brinks group, University of California)

Thieme Schmidt

Lars van Roemburg (TU Delft - Education and Student Affairs)

Bing Xu (TU Delft - RST/Applied Radiation & Isotopes)

Chun Ting Cho (TU Delft - RST/Energy Materials)

Liedewij Laan (TU Delft - BN/Liedewij Laan Lab)

Miao Ping Chien (Erasmus MC, Oncode Institute)

Daan Brinks (Erasmus MC, TU Delft - ImPhys/Brinks group)

DOI related publication
https://doi.org/10.1002/adma.202501944 Final published version
More Info
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Publication Year
2026
Language
English
Journal title
Advanced Materials
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Abstract

This study shows that coupling to designed plasmonic nanoparticles can modulate the electrophysiological function of proteins in living mammalian cells. Nanostar-shaped particles, that are robust to biological noise, are designed to enable near-field-coupling to plasma membrane-localized mutated Archaerhodopsin proteins in live cells. The coupled rhodopsins exhibit enhanced fluorescence and an increased response speed to membrane voltage. Incorporating this plasmonic enhancement into a Markov chain photocycle model of the Archaerhodopsin mutant QuasAr6a, shows an increased fluorescence emission rate and manipulation of the protein dynamics through a combination of photocycle transition rate enhancements. The results show an improvement in fluorescence and voltage-response dynamics of the functional QuasAr6a Archaerhodopsin mutant, beyond what has been achievable through genetic engineering. This opens up possibilities for engineering the biological functionality of proteins through plasmonics: manipulating protein photocycles could improve light sensitivity, change optogenetic applications, and lead to fluorescent biosensors with enhanced dynamics.