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Updated: Mar 13, 2026

How to Quantify the Fraction of Photoactivated Fluorescent Proteins in Bulk and in Live Cells
Published on: January 7, 2019
Photoswitchable Fluorescent Proteins: Do Not Always Look on the Bright Side
Karin Nienhaus1, Gerd Ulrich Nienhaus1,2,3,4
1Institute of Applied Physics, Karlsruhe Institute of Technology , 76131 Karlsruhe, Germany.
Abstract:
Photoactivatable fluorescent proteins (FPs) have become essential markers for nanoscopy on live specimens. In this issue of ACS Nano, Wang et al. present a reversibly photoswitching FP, GMars-Q, which they promote as an advanced marker for RESOLFT imaging because of its low residual intensity in the off state and low switching fatigue. Here, we explain the observed peculiar photobleaching behavior of GMars-Q by a mechanism that involves efficient shelving of proteins in dark states, resulting in low switching fatigue and low residual off intensity. There is a continuing demand for novel FP markers with properties optimized for specific imaging techniques. Endeavors to engineer such proteins can greatly benefit from increased efforts to acquire deeper mechanistic understanding of their photophysics and photochemistry.
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