ACS Nano,
Journal Year:
2017,
Volume and Issue:
11(6), P. 5598 - 5613
Published: May 17, 2017
We
report
the
development
of
a
quantum
dot
(QD)–peptide–fullerene
(C60)
electron
transfer
(ET)-based
nanobioconjugate
for
visualization
membrane
potential
in
living
cells.
The
bioconjugate
is
composed
(1)
central
QD
donor,
(2)
membrane-inserting
peptidyl
linker,
and
(3)
C60
acceptor.
photoexcited
donor
engages
ET
with
acceptor,
resulting
quenching
photoluminescence
(PL)
that
tracks
positively
number
moieties
arrayed
around
QD.
nature
QD-capping
ligand
also
modulates
efficiency;
neutral
coating
facilitates
greater
than
negatively
charged
carboxylated
ligand.
Steady-state
photophysical
characterization
confirms
an
ET-driven
process
between
donor–acceptor
pair.
When
introduced
to
cells,
amphiphilic
QD–peptide–C60
labels
plasma
by
insertion
peptide–C60
portion
into
hydrophobic
bilayer,
while
hydrophilic
sits
on
exofacial
side
membrane.
Depolarization
cellular
augments
process,
which
manifested
as
further
PL.
demonstrate
HeLa
PC12
primary
cortical
neurons
significant
PL
(ΔF/F0
2–20%
depending
QD–C60
separation
distance)
response
depolarization
KCl.
Further,
we
show
ability
use
probe
combination
conventional
voltage-sensitive
dyes
(VSDs)
simultaneous
two-channel
imaging
potential.
In
vivo
electrical
stimulation,
optical
optimal
configuration
exhibits
temporal
responsivity
stimulation
similar
VSDs.
Notably,
however,
construct
displays
20-
40-fold
ΔF/F0
tractable
system
offers
advantages
ease
assembly,
large
ΔF/F0,
enhanced
photostability,
high
throughput
without
need
complicated
organic
synthesis
or
genetic
engineering,
respectively,
required
traditional
VSDs
fluorescent
protein
constructs.
Journal of the American Chemical Society,
Journal Year:
2016,
Volume and Issue:
138(30), P. 9365 - 9368
Published: July 15, 2016
Here
we
present
a
far-red,
silicon-rhodamine-based
fluorophore
(SiR700)
for
live-cell
multicolor
imaging.
SiR700
has
excitation
and
emission
maxima
at
690
715
nm,
respectively.
SiR700-based
probes
F-actin,
microtubules,
lysosomes,
SNAP-tag
are
fluorogenic,
cell-permeable,
compatible
with
superresolution
microscopy.
In
conjunction
based
on
the
previously
introduced
carboxy-SiR650,
permit
microscopy
in
thus
significantly
expanding
our
capacity
imaging
living
cells.
Angewandte Chemie International Edition,
Journal Year:
2019,
Volume and Issue:
59(33), P. 13734 - 13762
Published: Oct. 12, 2019
Emerging
from
the
origins
of
supramolecular
chemistry
and
development
selective
chemical
receptors
that
rely
on
lock-and-key
binding,
activity-based
sensing
(ABS)-which
utilizes
molecular
reactivity
rather
than
recognition
for
analyte
detection-has
rapidly
grown
into
a
distinct
field
to
investigate
production
regulation
species
mediate
biological
signaling
stress
pathways,
particularly
metal
ions
small
molecules.
Chemical
reactions
exploit
diverse
enable
sensitive
synthetic
methods
decipher
their
contributions
within
complex
living
environments.
The
broad
utility
this
reaction-driven
approach
facilitates
application
imaging
platforms
ranging
fluorescence,
luminescence,
photoacoustic,
magnetic
resonance,
positron
emission
tomography
modalities.
ABS
are
also
being
expanded
other
fields,
such
as
drug
materials
discovery.
Annual Review of Biochemistry,
Journal Year:
2017,
Volume and Issue:
86(1), P. 825 - 843
Published: April 12, 2017
Small-molecule
fluorophores,
such
as
fluorescein
and
rhodamine
derivatives,
are
critical
tools
in
modern
biochemical
biological
research.
The
field
of
chemical
dyes
is
old;
colored
molecules
were
first
discovered
the
1800s,
scaffolds
have
been
known
for
over
a
century.
Nevertheless,
there
has
renaissance
using
these
to
create
biochemistry
biology.
application
chemistry,
biochemistry,
molecular
genetics,
optical
physics
old
structures
enables
drives
development
novel,
sophisticated
fluorescent
dyes.
This
review
focuses
on
an
important
example
biology-the
melding
new
knowledge-leading
useful
advanced
experiments.
Journal of the American Chemical Society,
Journal Year:
2021,
Volume and Issue:
143(41), P. 17136 - 17143
Published: Oct. 11, 2021
Fluorescence
bioimaging
through
the
second
near-infrared
window
(NIR-II,
1000–1700
nm)
has
attracted
much
attention
due
to
its
deep
penetration
and
high
contrast.
However,
exploring
new
fluorescent
materials,
especially
small
molecular
fluorophores
with
long
wavelength
brightness,
is
still
quite
challenging.
By
expanding
π-conjugation
enhancing
intramolecular
charge
transfer
effect,
herein
we
report
a
series
of
xanthene-based
NIR-II
dyes,
named
VIXs.
Among
these
VIX-4
exhibits
best
performance
fluorescence
emission
at
1210
nm
brightness
been
used
for
dynamically
imaging
blood
flow
mice
200
fps.
virtue
spatiotemporal
resolution
dynamic
imaging,
can
distinguish
directly
artery
vein
direction
measure
volume
by
videos.
This
study
provides
not
only
an
effective
tool
spatial
temporal
but
also
promising
conjugated
skeleton
dyes.
Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
124(4), P. 1738 - 1861
Published: Feb. 14, 2024
The
microenvironment
is
indispensable
for
functionality
of
various
biomacromolecules,
subcellular
compartments,
living
cells,
and
organisms.
In
particular,
physical
properties
within
the
biological
could
exert
profound
effects
on
both
cellular
physiology
pathology,
with
parameters
including
polarity,
viscosity,
pH,
other
relevant
factors.
There
a
significant
demand
to
directly
visualize
quantitatively
measure
fluctuation
in
spatiotemporal
resolution.
To
satisfy
this
need,
analytical
methods
based
fluorescence
probes
offer
great
opportunities
due
facile,
sensitive,
dynamic
detection
that
these
molecules
enable
varying
settings
from
vitro
samples
live
animal
models.
Herein,
we
focus
types
small
molecule
fluorescent
measurement
microenvironment,
mechanical
force,
temperature,
electron
potential.
For
each
parameter,
primarily
describe
chemical
mechanisms
underlying
how
are
correlated
changes
signals.
This
review
provides
an
overview
perspective
development
environment,
expand
knowledge
process,
enrich
diagnostic
tools
human
diseases.
Science,
Journal Year:
2023,
Volume and Issue:
379(6639)
Published: March 31, 2023
It
is
known
that
interactions
between
nociceptors
and
dendritic
cells
(DCs)
can
modulate
immune
responses
in
barrier
tissues.
However,
our
understanding
of
the
underlying
communication
frameworks
remains
rudimentary.
Here,
we
show
control
DCs
three
molecularly
distinct
ways.
First,
release
calcitonin
gene-related
peptide
imparts
a
transcriptional
profile
on
steady-state
characterized
by
expression
pro-interleukin-1β
other
genes
implicated
DC
sentinel
functions.
Second,
nociceptor
activation
induces
contact-dependent
calcium
fluxes
membrane
depolarization
enhances
their
production
proinflammatory
cytokines
when
stimulated.
Finally,
nociceptor-derived
chemokine
CCL2
contributes
to
orchestration
DC-dependent
local
inflammation
induction
adaptive
against
skin-acquired
antigens.
Thus,
combined
actions
chemokines,
neuropeptides,
electrical
activity
fine-tune