posted on 2012-09-12, 00:00authored byOksana
M. Subach, David Entenberg, John S. Condeelis, Vladislav V. Verkhusha
Fluorescent proteins photoswitchable with noncytotoxic
light irradiation
and spectrally distinct from multiple available photoconvertible green-to-red
probes are in high demand. We have developed a monomeric fluorescent
protein, called PSmOrange2, which is photoswitchable with blue light
from an orange (ex./em. at 546 nm/561 nm) to a far-red (ex./em. at
619 nm/651 nm) form. Compared to another orange-to-far-red photoconvertable
variant, PSmOrange2 has blue-shifted photoswitching action spectrum,
9-fold higher photoconversion contrast, and up to 10-fold faster photoswitching
kinetics. This results in the 4-fold more PSmOrange2 molecules being
photoconverted in mammalian cells. Compared to common orange fluorescent
proteins, such as mOrange, the orange form of PSmOrange has substantially
higher photostability allowing its use in multicolor imaging applications
to track dynamics of multiple populations of intracellular objects.
The PSmOrange2 photochemical properties allow its efficient photoswitching
with common two-photon lasers and, moreover, via Förster resonance
energy transfer (FRET) from green fluorescent donors. We have termed
the latter effect a FRET-facilitated photoswitching and demonstrated
it using several sets of interacting proteins. The enhanced photoswitching
properties of PSmOrange2 make it a superior photoconvertable protein
tag for flow cytometry, conventional microscopy, and two-photon imaging
of live cells.