Small Methods,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 24, 2024
DNA,
as
natural
polymers,
not
only
serves
the
genetic
material
but
also
shows
great
potential
assistants
for
efficient
and
targeted
nanoparticle
separation.
This
is
due
to
its
high
programmability,
excellent
biocompatibility,
stability
effectively
binding
with
various
types
of
nanoparticles
or
bioparticles,
while
modifying
physical
properties
target
particles
such
charge,
mass
size.
Researchers
have
achieved
remarkable
efficiency
in
separating
by
precisely
designing
DNA
sequences
their
interactions
particles.
achievement
primarily
relies
on
differences
medium
modulated
DNA.
In
this
minireview,
diverse
strategies
are
overviewed
using
assist
separation,
applications
these
separation
highlighted.
Finally,
current
challenges
prospects
DNA-assisted
discussed.
Nano Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 27, 2025
Precise
imaging
of
noncoding
RNAs
(ncRNAs)
in
specific
organelles
allows
decoding
their
functions
at
subcellular
level
but
lacks
advanced
tools.
Here
we
present
a
DNA-based
nanobiotechnology
for
spatially
selective
ncRNA
(e.g.,
microRNA
(miRNA))
mitochondria
via
an
organelle-specific
DNA
assembly
strategy.
The
target
miRNA-initiated
hairpins
is
inhibited
by
the
block
toehold-mediated
strand
displacement
reaction
can
be
exclusively
activated
mitochondria-encoded
ribosomal
RNA
(rRNA)
hybridization
chain
reaction,
enabling
spatial
control
over
miRNA
imaging.
We
demonstrate
that
conditionally
controlled
technology
minimization
nonspecific
activation
and
thus
improves
precision
detection.
In
addition,
strategy
adaptable
to
visualizing
other
ncRNAs
such
as
long
mitochondria,
highlighting
universality
approach.
Overall,
this
work
provides
useful
tool
investigating
organelle-located
RNA.
Molecules,
Journal Year:
2025,
Volume and Issue:
30(5), P. 1025 - 1025
Published: Feb. 24, 2025
Mitochondria,
as
vital
organelles,
play
a
central
role
in
subcellular
research
and
biomedical
innovation.
Although
functional
nucleic
acid
(FNA)
nanostructures
have
witnessed
remarkable
progress
across
numerous
biological
applications,
strategies
specifically
tailored
to
target
mitochondria
for
molecular
imaging
therapeutic
interventions
remain
scarce.
This
review
delves
into
the
latest
advancements
leveraging
FNA
mitochondria-specific
cancer
therapy.
Initially,
we
explore
creation
of
FNA-based
biosensors
localized
mitochondria,
enabling
real-time
detection
visualization
critical
molecules
essential
mitochondrial
function.
Subsequently,
examine
developments
aimed
at
mitochondrial-targeted
treatments,
including
modular
nanodevices
precise
delivery
agents
programmable
disrupting
processes.
Emphasis
is
placed
on
elucidating
chemical
principles
underlying
design
mitochondrial-specific
nanotechnology
diverse
uses.
Lastly,
address
unresolved
challenges
outline
prospective
directions,
with
goal
advancing
field
encouraging
sophisticated
tools
both
academic
inquiry
clinical
applications
centered
mitochondria.
Small Methods,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 26, 2025
Fluorescence
imaging
has
been
a
powerful
technique
for
the
visualization
of
interest
biomolecules.
It
is
widely
used
in
basic
biological
research,
clinical
medicine,
and
other
fields.
However,
fluorescence
signals
are
often
too
weak
detecting
with
simple
devices
or
complex
environments.
Besides,
limited
to
about
four
six
dyes,
restricting
spectral
overlap
organic
fluorophores.
DNA
nanotechnology
including
structured
dynamic
emerges
as
promising
material
encode
fluorophores,
holding
great
potential
improve
properties
signals.
Substantial
progresses
have
achieved
DNA-encoded
signals,
exhibiting
novel
characteristics
applications.
This
review
summarizes
various
encoding
strategies
their
performance
analysis.
In
this
review,
different
methods
impacts
on
reported,
such
brightness,
photostability,
kinetics,
multiplexing.
application
reviewed.
Finally,
solutions
address
current
challenges
suggested,
encouraging
future
development
area.
Analytical Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 26, 2025
Engineering
deoxyribozymes
under
extreme
conditions
will
expand
their
repertoires
for
unique
applications.
Although
all
known
deoxyribozyme-based
biosensors
were
derived
to
function
or
near
physiological
conditions,
no
prior
study
has
been
conducted
purposely
build
them
absolutely
atypical
conditions.
Here,
we
reported
the
design
and
characterization
of
an
acidic
RNA-cleaving
deoxyribozyme,
termed
ET46,
that
displays
strongly
cooperative
H+
binding
performing
catalysis
at
pH,
yielding
a
Hill
coefficient
5.4.
This
feature
cooperativity
significantly
improves
responsiveness
ET46
small
pH
variations
within
range
4.5-5.5.
We
further
exploited
pH-sensitive
properties
track
changes
on
uptake
localization
in
lysosomes.
Finally,
developed
lysosomal
ATP-activated
fluorescence-signaling
aptazyme
biosensor
(named
FabATP)
using
ATP-binding
DNA
aptamer.
To
demonstrate
its
ability
lysosomes,
applied
FabATP
live
subcellular
fluorescence
imaging
ATP
fluctuations
upon
stimulations.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 31, 2024
Abstract
Although
DNAzyme
sensors
have
been
widely
developed
for
imaging
metal
ions,
their
application
in
specific
subcellular
compartments
remains
challenging
due
to
low
spatial
controllability.
Here
we
present
a
locally
activatable,
DNAzyme‐based
sensing
technology
that
enables
compartment‐specific
of
ions
through
ribosomal
RNA
(rRNA)
regulated
signal
amplification.
The
system
leverages
subcellularly
encoded
rRNA
activate
sensors,
and
further
drives
amplification
via
multiple
turnover
cleavage
molecular
beacons,
significantly
enhance
sensitivity
precision
metal‐ion
organelles
(e.g.
mitochondria)
or
membraneless
cytosol).
Furthermore,
demonstrate
the
allows
situ
monitoring
dynamics
mitochondrial
Zn
2+
during
ischemia
drug
intervention.
This
study
expands
toolbox
investigating
role
disease
processes.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 31, 2024
Although
DNAzyme
sensors
have
been
widely
developed
for
imaging
metal
ions,
their
application
in
specific
subcellular
compartments
remains
challenging
due
to
low
spatial
controllability.
Here
we
present
a
locally
activatable,
DNAzyme-based
sensing
technology
that
enables
compartment-specific
of
ions
through
ribosomal
RNA
(rRNA)
regulated
signal
amplification.
The
system
leverages
subcellularly
encoded
rRNA
activate
sensors,
and
further
drives
amplification
via
multiple
turnover
cleavage
molecular
beacons,
significantly
enhance
sensitivity
precision
metal-ion
organelles
(e.g.
mitochondria)
or
membraneless
cytosol).
Furthermore,
demonstrate
the
allows
situ
monitoring
dynamics
mitochondrial
Zn
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(42), P. 16971 - 16977
Published: Oct. 11, 2024
The
development
of
highly
sensitive
and
precise
imaging
techniques
capable
visualizing
crucial
molecules
at
the
subcellular
level
is
essential
for
elucidating
mitochondrial
functions
uncovering
novel
mechanisms
in
biological
processes.
However,
traditional
molecular
strategies
are
still
limited
by
off-mitochondria
signal
leakage
because
"always-active"
sensing
mode.
To
address
this
limitation,
we
have
developed
a
light-triggered
activation
sequence
activated
plasmonic
DNAzyme
walker
(PDW)
accurate
combination
an
organelle
localized
strategy,
upconversion
nanotechnology,
plasmon
enhanced
fluorescence
(PEF)
technique.
Exploiting
advantage
light
enables
control
over
when
where
to
activate
probe's
function,
effectively
reducing
as
validated
dynamic
monitoring
changes
signals
during
entry
process.
Furthermore,
leveraging
PEF
capability
triangular
gold
nanoprisms
(Au
NPRs),
intensity
can
be
approximately
11.9
times,
ensuring
imaging.
Small Methods,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 14, 2024
Abstract
Live‐cell
imaging
of
RNA
in
specific
subcellular
compartments
is
essential
for
elucidating
the
rich
repertoire
cellular
functions,
but
it
has
been
limited
by
a
lack
simple,
precisely
controlled
methods.
Here
such
an
approach
presented
via
combination
hybridization
chain
reaction
and
spatially
restricted
enzymatic
activation
with
organelle‐targeted
delivery.
The
system
can
localize
engineered
DNA
hairpins
mitochondria,
where
target
RNA‐initiated
events
selectively
activated
enzyme,
enabling
amplified
high
precision.
It
demonstrated
that
compatible
live
cell
visualization
enables
regulatable
microRNA
mitochondria.
Since
situ
signal
amplification
enzyme
eliminates
need
genetically
encoded
protein
overexpression,
envisioned
this
simple
platform
will
be
broadly
applicable
precise
resolution
variety
biological
processes.