Angewandte Chemie,
Journal Year:
2023,
Volume and Issue:
136(4)
Published: Dec. 1, 2023
Abstract
Encoded
nanostructures
afford
an
ideal
platform
carrying
multi‐channel
signal
components
for
multiplexed
assay
and
information
security.
However,
with
the
demand
on
exclusivity
reproducibility
of
coding
signals,
precise
control
structure
composition
nanomaterials
featuring
fully
distinguishable
signals
remains
challenging.
By
using
multiplexing
capability
mass
spectrometry
(MS)
spatial
addressability
DNA
origami
nanostructures,
we
herein
propose
a
quality
methodology
constructing
mass‐encoded
nanodevices
(namely
MNTs‐TDOFs)
in
scaffold
compartmented
tetrahedral
frames
(TDOFs),
which
arrangement
stoichiometry
four
types
nanotags
(MNTs)
can
be
finely
regulated
customized
to
generate
characteristic
MS
patterns.
The
programmability
combinatorial
MNTs
orthogonality
individual
compartments
allows
further
evolution
MNTs‐TDOFs
static
tagging
agents
dynamic
nanoprobes
labeling
sensing
multiple
targets.
More
importantly,
at
single
TDOF
level
ensures
constancy
prescribed
outputs,
by
high‐capacity
system
was
established
secure
encryption
decryption.
In
addition
outputs
parallel,
could
also
map
logic
circuits
interconnected
complexity
events
c‐Met
recognition
dimerization
cell
surface
signaling
regulation
interrogation.
Nano Letters,
Journal Year:
2024,
Volume and Issue:
24(28), P. 8732 - 8740
Published: July 3, 2024
Piwi-interacting
RNAs
(piRNAs)
are
small
noncoding
that
repress
transposable
elements
to
maintain
genome
integrity.
The
canonical
catalytic
hairpin
assembly
(CHA)
circuit
relies
on
random
collisions
of
free-diffused
reactant
probes,
which
substantially
slow
down
reaction
efficiency
and
kinetics.
Herein,
we
demonstrate
the
construction
a
spatial-confined
self-stacking
for
rapid
sensitive
imaging
piRNA
in
living
cells
based
intramolecular
intermolecular
hybridization-accelerated
CHA.
We
rationally
design
3WJ
probe
not
only
accelerates
kinetics
by
increasing
local
concentration
probes
but
also
eliminates
background
signal
leakage
caused
cross-entanglement
preassembled
probes.
This
strategy
achieves
high
sensitivity
good
specificity
with
shortened
assay
time.
It
can
quantify
intracellular
expression
at
single-cell
level,
discriminate
tissues
breast
cancer
patients
healthy
persons,
situ
image
cells,
offering
new
approach
early
diagnosis
postoperative
monitoring.
Nano Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 17, 2024
MicroRNAs
(MiRNAs)
are
valuable
biomarkers
for
the
diagnosis
and
prognosis
of
diseases.
The
development
reliable
assays
is
an
urgent
pursuit.
We
herein
fabricate
a
novel
electrochemical
sensing
strategy
based
on
conformation
transitions
DNA
nanostructures
click
chemistry.
Duplex-specific
nuclease
(DSN)-catalyzed
reaction
first
used
disintegration
triangular
pyramid
frustum
(DNA
TPF).
A
triangle
formed,
which
in
turn
assists
strain-promoted
alkyne-azide
cycloaddition
(SPAAC)
to
localize
single-stranded
probes
(P1).
After
SPAAC
ligation,
multiple
hairpins
spontaneously
folded,
labeled
species
dragged
near
electrode
interface.
By
recording
analyzing
responses,
highly
sensitive
biosensor
established,
exhibits
high
sensitivity
reproducibility.
Clinical
applications
have
been
verified
with
good
stability.
This
relies
integration
chemistry,
may
inspire
further
designs
nanotechnology
clinical
Advanced Healthcare Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 29, 2025
Abstract
Developing
nanoscale
platforms
with
high
integration,
assembly
efficiency,
and
structural
stability
for
performing
complex
computations
in
specific
cells
remains
a
significant
challenge.
To
address
this,
the
Three‐dimensional
Hierarchical
Octahedral
Robotic
(THOR)
DNA
nanoplatform
is
introduced,
which
integrates
targeting,
logic
computation,
sensing
modules
within
single
framework.
This
specifically
binds
to
cancer
cell
surface
proteins,
releasing
aptamer‐linked
fuel
chains
initiate
subsequent
computational
processes.
Three
gates
efficiently
compute
any
arbitrary
binary
combination
of
target
proteins.
The
module
employs
catalytic
hairpin
detecting
miRNAs
sensitivity.
THOR
demonstrates
robust
functionality
both
vitro
situ.
As
proof‐of‐concept,
this
distinguish
acute
lymphoblastic
leukemia
(ALL)
patients
from
other
subtypes
healthy
participants,
achieving
100%
accuracy
applied.
Additionally,
approach
reliably
monitored
therapeutic
progress
ALL
patients,
showing
strong
concordance
bone
marrow
smear
results.
platform
highlights
feasibility
constructing
reliable,
hierarchical,
multifunctional
analytical
system
based
on
polyhedron.
It
offers
promising
auxiliary
tool
clinical
diagnostics
monitoring.
Analytical Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 14, 2025
mRNA,
a
critical
biomarker
for
various
diseases
and
promising
target
cancer
therapy,
is
central
to
biological
medical
research.
However,
the
development
of
multiplexed
approaches
in
situ
monitoring
mRNA
live
cells
are
limited
by
their
reliance
on
enzyme-based
signal
amplification,
challenges
with
diffusion,
complexity
nucleic
acid
design.
In
this
study,
we
introduce
nonenzymatic
catalytic
DNA
assembly
(NEDA)
technique
address
these
limitations.
NEDA
facilitates
precise
imaging
intracellular
assembling
three
free
hairpin
amplifiers
into
low-mobility,
three-dimensional
spherical
structure.
This
approach
also
enables
simultaneous
detection
four
distinct
targets
via
combination
fluorescent
signals,
limit
as
low
141.2
pM
mRNA.
To
enhance
efficiency
design,
employed
computer-aided
design
(CAD)
rapidly
generate
feasible
sequences
highly
detection.
By
integrating
machine
learning
algorithms,
achieved
impressive
accuracy
nearly
96.66%
distinguishing
multiple
cell
types
87.80%
identifying
same
type
under
different
drug
stimulation
conditions.
Notably,
our
platform
can
identify
stimuli
similar
mechanisms
action,
highlighting
its
potential
development.
3D
sensing
strategy
CAD
not
only
enhances
ability
image
simultaneously
but
provides
novel
efficient
molecular
diagnostics
personalized
therapy.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
63(4)
Published: Dec. 1, 2023
Abstract
Encoded
nanostructures
afford
an
ideal
platform
carrying
multi‐channel
signal
components
for
multiplexed
assay
and
information
security.
However,
with
the
demand
on
exclusivity
reproducibility
of
coding
signals,
precise
control
structure
composition
nanomaterials
featuring
fully
distinguishable
signals
remains
challenging.
By
using
multiplexing
capability
mass
spectrometry
(MS)
spatial
addressability
DNA
origami
nanostructures,
we
herein
propose
a
quality
methodology
constructing
mass‐encoded
nanodevices
(namely
MNTs‐TDOFs)
in
scaffold
compartmented
tetrahedral
frames
(TDOFs),
which
arrangement
stoichiometry
four
types
nanotags
(MNTs)
can
be
finely
regulated
customized
to
generate
characteristic
MS
patterns.
The
programmability
combinatorial
MNTs
orthogonality
individual
compartments
allows
further
evolution
MNTs‐TDOFs
static
tagging
agents
dynamic
nanoprobes
labeling
sensing
multiple
targets.
More
importantly,
at
single
TDOF
level
ensures
constancy
prescribed
outputs,
by
high‐capacity
system
was
established
secure
encryption
decryption.
In
addition
outputs
parallel,
could
also
map
logic
circuits
interconnected
complexity
events
c‐Met
recognition
dimerization
cell
surface
signaling
regulation
interrogation.
Smart Molecules,
Journal Year:
2023,
Volume and Issue:
1(3)
Published: Dec. 1, 2023
Abstract
Molecular
subtyping
of
cancer
can
greatly
help
to
understand
the
development
disease
and
predict
tumor
behavior.
Exploring
detection
methods
for
precise
is
appealing
prognosis
personalized
therapy.
During
past
decades,
DNA‐based
biosensors
have
exhibited
great
potential
in
diagnosis
due
their
structural
programmability
functional
diversity.
Despite
encouraging
progress
that
has
been
made,
there
remains
an
issue
improving
accuracy
sensitivity
complex
process
disease,
especially
preclinical
or
clinical
applications.
To
accelerate
DNA
sensors
identification
subtypes,
this
review,
we
summarized
advances
molecular
by
analyzing
heterogeneity
categories
levels
biomarkers
between
subtypes.
The
strategies
toward
genomic
proteomic
cells
on
cell
surface,
as
well
excretions
including
extracellular
vesicles
(EVs)
microRNA
(miRNAs)
serum,
are
summarized.
Current
challenges
opportunities
field
also
discussed.
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(21), P. 8754 - 8762
Published: May 13, 2024
Simultaneous
profiling
of
redox-regulated
markers
at
different
cellular
sublocations
is
great
significance
for
unraveling
the
upstream
and
downstream
molecular
mechanisms
oxidative
stress
in
living
cells.
Herein,
by
synchronizing
dual
target-triggered
DNA
machineries
one
nanoentity,
we
engineered
a
walker-driven
mass
nanotag
(MNT)
assembly
system
(w-MNT-AS)
that
can
be
sequentially
activated
stress-associated
mucin
1
(MUC1)
apurinic/apyrimidinic
endonuclease
(APE1)
from
plasma
membrane
to
cytoplasm
induce
recycled
MNTs
multiplex
detection
two
matrix-assisted
laser
desorption
ionization
spectrometry
(MALDI
MS).
In
working
cascade,
sensing
process
governs
separate
activation
w-MNT-AS
MUC1
APE1
diverse
locations,
while
contributes
parallel
amplification
ion
signal
characteristic
tags.
this
manner,
differences
between
MCF-7,
HeLa,
HepG2,
L02
cells
expression
cytoplasmic
were
fully
characterized.
Furthermore,
level
dynamics
caused
exogenous
H2O2,
doxorubicin,
simvastatin
comprehensively
demonstrated
tracking
fate
across
locations.
The
proposed
coupled
MS
method
provides
an
effective
route
probe
multiple
functional
molecules
lie
locations
participating
same
event,
facilitating
mechanistic
studies
on
response
other
disease-related
processes.