Plasmonic Enhancement of Fluorescence and Protein Dynamics in Living Mammalian Cells
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)
More Info
expand_more
Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.
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.