Chemical Science,
Journal Year:
2020,
Volume and Issue:
11(32), P. 8506 - 8516
Published: Jan. 1, 2020
Cyclooctatetraene-conjugated
cyanine
dyes
represent
an
effective
strategy
to
improve
biocompatibility
under
light
in
live-cell
fluorescence
imaging
and
analysis
of
mitochondria.
Organic & Biomolecular Chemistry,
Journal Year:
2020,
Volume and Issue:
18(30), P. 5747 - 5763
Published: Jan. 1, 2020
Guidelines
based
on
photophysical
tuning,
reactivity,
isomerization,
and
energy
transfer
for
rational
design
of
synthetic
fluorescent
probes
biological
systems.
Journal of the American Chemical Society,
Journal Year:
2020,
Volume and Issue:
142(42), P. 17828 - 17844
Published: Oct. 9, 2020
Single-molecule
super-resolution
microscopy
has
developed
from
a
specialized
technique
into
one
of
the
most
versatile
and
powerful
imaging
methods
nanoscale
over
past
two
decades.
In
this
perspective,
we
provide
brief
overview
historical
development
field,
fundamental
concepts,
methodology
required
to
obtain
maximum
quantitative
information,
current
state
art.
Then,
will
discuss
emerging
perspectives
areas
where
innovation
further
improvement
are
needed.
Despite
tremendous
progress,
full
potential
single-molecule
is
yet
be
realized,
which
enabled
by
research
ahead
us.
Journal of the American Chemical Society,
Journal Year:
2021,
Volume and Issue:
143(36), P. 14592 - 14600
Published: Aug. 30, 2021
Rhodamines
are
the
most
important
class
of
fluorophores
for
applications
in
live-cell
fluorescence
microscopy.
This
is
mainly
because
rhodamines
exist
a
dynamic
equilibrium
between
fluorescent
zwitterion
and
nonfluorescent
but
cell-permeable
spirocyclic
form.
Different
imaging
require
different
positions
this
equilibrium,
an
adjustment
poses
challenge
design
suitable
probes.
We
describe
here
how
conversion
ortho-carboxy
moiety
given
rhodamine
into
substituted
acyl
benzenesulfonamides
alkylamides
permits
systematic
tuning
spirocyclization
with
unprecedented
accuracy
over
large
range.
allows
one
to
transform
same
either
highly
fluorogenic
probe
live-cell-stimulated
emission
depletion
(STED)
microscopy
or
spontaneously
blinking
dye
single-molecule
localization
(SMLM).
used
approach
generate
differently
colored
probes
optimized
labeling
systems
applications.
Nature Methods,
Journal Year:
2021,
Volume and Issue:
19(1), P. 65 - 70
Published: Dec. 16, 2021
Abstract
Self-labeling
protein
tags
such
as
HaloTag
are
powerful
tools
that
can
label
fusion
proteins
with
synthetic
fluorophores
for
use
in
fluorescence
microscopy.
Here
we
introduce
variants
either
increased
or
decreased
brightness
and
lifetime
compared
HaloTag7
when
labeled
rhodamines.
Combining
these
enabled
live-cell
multiplexing
of
three
cellular
targets
one
spectral
channel
using
a
single
fluorophore
the
generation
lifetime-based
biosensor.
Additionally,
brightest
variant
showed
up
to
40%
higher
imaging
applications.
Cell,
Journal Year:
2022,
Volume and Issue:
185(18), P. 3390 - 3407.e18
Published: Sept. 1, 2022
Chemical
synapses
between
axons
and
dendrites
mediate
neuronal
intercellular
communication.
Here,
we
describe
a
synapse
primary
cilia:
the
axo-ciliary
synapse.
Using
enhanced
focused
ion
beam-scanning
electron
microscopy
on
samples
with
optimally
preserved
ultrastructure,
discovered
brainstem
serotonergic
cilia
of
hippocampal
CA1
pyramidal
neurons.
Functionally,
these
are
enriched
in
ciliary-restricted
serotonin
receptor,
5-hydroxytryptamine
receptor
6
(5-HTR6).
cilia-targeted
sensor,
show
that
opto-
chemogenetic
stimulation
releases
onto
cilia.
Ciliary
5-HTR6
activates
non-canonical
G
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: April 27, 2022
Abstract
The
quality
and
application
of
super-resolution
fluorescence
imaging
greatly
lie
in
the
dyes’
properties,
including
photostability,
brightness,
Stokes
shift.
Here
we
report
a
synergistic
strategy
to
simultaneously
improve
such
properties
regular
fluorophores.
Introduction
quinoxaline
motif
with
fine-tuned
electron
density
conventional
rhodamines
generates
new
dyes
vibration
structure
inhibited
twisted-intramolecular-charge-transfer
(TICT)
formation
synchronously,
thus
increasing
brightness
photostability
while
enlarging
fluorophore
YL578
exhibits
around
twofold
greater
shift
than
its
parental
fluorophore,
Rhodamine
B.
Importantly,
Stimulated
Emission
Depletion
(STED)
microscopy,
derived
probe
possesses
superior
renders
threefold
more
frames
carbopyronine
based
probes
(CPY-Halo
580CP-Halo),
known
as
photostable
fluorophores
for
STED
imaging.
Furthermore,
is
well
generalized
offer
class
bright
fluorescent
long
(up
136
nm)
bioimaging
biosensing.