A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling
Author(s) -
Rita Strack,
Birka Hein,
Dibyendu Bhattacharyya,
Stefan W. Hell,
Robert J. Keenan,
Benjamin S. Glick
Publication year - 2009
Publication title -
biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.43
H-Index - 253
eISSN - 1520-4995
pISSN - 0006-2960
DOI - 10.1021/bi900870u
Subject(s) - far red , fluorescence , red light , flow cytometry , derivative (finance) , red cell , biophysics , chemistry , biology , optics , physics , microbiology and biotechnology , botany , computer science , computer security , financial economics , economics
Fluorescent proteins (FPs) with far-red excitation and emission are desirable for multicolor labeling and live-animal imaging. We describe E2-Crimson, a far-red derivative of the tetrameric FP DsRed-Express2. Unlike other far-red FPs, E2-Crimson is noncytotoxic in bacterial and mammalian cells. E2-Crimson is brighter than other far-red FPs and matures substantially faster than other red and far-red FPs. Approximately 40% of the E2-Crimson fluorescence signal is remarkably photostable. With an excitation maximum at 611 nm, E2-Crimson is the first FP that is efficiently excited with standard far-red lasers. We show that E2-Crimson has unique applications for flow cytometry and stimulated emission depletion (STED) microscopy.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom