Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(40), P. 15915 - 15923
Published: Sept. 26, 2024
Accurate
monitoring
of
base
excision
repair
(BER)
activity
in
cancer
cells
is
critical
for
advancing
the
comprehension
DNA
processes,
gaining
insights
into
development,
and
guiding
treatment
strategies.
However,
current
assay
techniques
assessing
BER
face
challenges
due
to
heterogeneous
origins
diversity
enzymes.
In
this
work,
we
present
a
hi
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(23), P. 9666 - 9675
Published: May 30, 2024
Epigenetic
modification
plays
an
indispensable
role
in
regulating
routine
molecular
signaling
pathways,
yet
it
is
rarely
used
to
modulate
self-assembly
networks.
Herein,
we
constructed
a
bioorthogonal
demethylase-stimulated
DNA
circuitry
(DSC)
system
for
high-fidelity
imaging
of
microRNA
(miRNA)
live
cells
and
mice
by
eliminating
undesired
off-site
signal
leakage.
The
simple
robust
DSC
composed
primary
cell-specific
regulation
(CR)
module
ultimate
signal-transducing
amplifier
(SA)
module.
After
the
modularly
designed
was
delivered
into
target
cells,
DNAzyme
CR
site-specifically
activated
endogenous
demethylase
produce
fuel
strands
subsequent
miRNA-targeting
SA
Through
on-site
multiply
guaranteed
recognitions,
lucid
efficient
realized
reliably
amplified
vivo
miRNA
sensing
enabled
in-depth
exploration
demethylase-involved
pathway
with
cells.
Our
bioorthogonally
on-site-activated
represents
universal
versatile
biomolecular
platform
via
various
regulations
shows
more
prospects
different
personalized
theragnostics.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
Inspired
by
naturally
occurring
protein
dimerization
networks,
in
which
a
set
of
proteins
interact
with
each
other
to
achieve
highly
complex
input-output
behaviors,
we
demonstrate
here
fully
synthetic
DNA-based
network
that
enables
programmable
computations.
Our
consists
DNA
oligonucleotide
monomers
modified
reactive
moieties
can
covalently
bond
form
dimer
outputs
an
all-to-all
or
many-to-many
fashion.
By
designing
input
strands
specifically
sequester
monomers,
control
the
size
reaction
and
thus
fine-tune
yield
output
predictable
manner.
Thanks
programmability
specificity
DNA–DNA
interactions,
show
this
approach
be
used
different
using
inputs.
The
is
also
versatile
networks
based
on
two
distinct
covalent
reactions:
thiol–disulfide
strain-promoted
azide–alkyne
cycloaddition
(SPAAC)
reactions.
Finally,
functional
output,
ultimately
controlling
assembly
disassembly
nanostructures.
dynamic
shown
provide
way
convert
multiple
inputs
into
broader
range
functions,
including
ones
mimic
those
living
cells.
Proceedings of the National Academy of Sciences,
Journal Year:
2024,
Volume and Issue:
121(34)
Published: Aug. 15, 2024
In
the
age
of
information
explosion,
exponential
growth
digital
data
far
exceeds
capacity
current
mainstream
storage
media.
DNA
is
emerging
as
a
promising
alternative
due
to
its
higher
density,
longer
retention
time,
and
lower
power
consumption.
To
date,
commercially
mature
synthesis
sequencing
technologies
allow
for
writing
reading
on
with
customization
convenience
at
research
level.
However,
under
disconnected
nonspecialized
mode,
encounters
practical
challenges,
including
susceptibility
errors,
long
latency,
resource-intensive
requirements,
elevated
security
risks.
Herein,
we
introduce
platform
named
DNA-DISK
that
seamlessly
streamlined
synthesis,
storage,
microfluidics
coupled
tabletop
device
automated
end-to-end
storage.
The
single-nucleotide
enzymatic
biocapping
strategy
utilized,
offering
an
ecofriendly
cost-effective
approach
writing.
A
encapsulation
using
thermo-responsive
agarose
developed
on-chip
solidification,
not
only
eliminating
clutter
but
also
preventing
degradation.
Pyrosequencing
employed
in
situ
accurate
reading.
As
proof
concept,
successfully
stored
retrieved
musical
sheet
file
(228
bits)
write-to-read
latency
(4.4
min
per
bit)
well
superior
automation
compared
other
platforms,
demonstrating
potential
evolve
into
Hard
Disk
Drive
future.
Multicolor
fluorescent
encryption
systems
that
respond
to
specific
stimuli
have
drawn
widespread
attention
data
storage
and
due
their
low
cost
facile
access.
However,
existing
are
limited
by
materials,
restricting
depth.
This
study
uses
DNA
molecules
as
materials
offer
exceptional
specificity
depth
within
sequences.
With
inkjet-printed
microarrays
on
a
solid-phase
interface,
multicolor
system
based
hybridization
strand
displacement
is
developed,
achieving
an
with
high
flexibility.
strands,
modified
different
labels,
delivered
onto
interfaces
containing
self-assembled
monolayer
(SAM)
via
inkjet
printing,
forming
microarrays.
Data
achieved
through
the
of
strands
for
presentation
interference
SAM
at
interface
between
solid
phase
droplets.
Interference
can
be
removed
decryption.
The
this
determined
design
sequences
combination
multiple
showcasing
its
outstanding
ability.
Meanwhile,
high-throughput
printing
accelerates
writing
process,
further
enhancing
efficiency.
reaction
in
microarrays,
provides
scalable
robust
strategy
high-depth
efficient
encryption.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 4, 2025
In
recent
years,
DNA
has
emerged
as
a
promising
molecule
for
the
construction
of
molecular
computing
systems.
research
field
logic
circuits,
enzyme-driven
which
offer
faster
reactions
and
lower
complexity,
have
become
key
focus
in
field.
However,
it
remains
significant
drawback
that
lacks
capability
being
reused.
Reusability
is
essential
to
enhance
computational
capacity,
correct
errors,
reduce
costs
circuits.
this
study,
we
propose
method
achieving
high
reuse
circuits
using
exonuclease
III.
By
selectively
digesting
ds-DNA
while
preserving
gate
strands,
our
system
highly
restores
circuit
its
initial
state,
contains
no
waste-strand.
This
demonstrated
good
performance
converted-input
experiment
single-gate,
multilayer
cascades.
Finally,
achieve
four
times
relatively
complex
three
multiple
square
root
circuit.
In
the
domain
of
digital
data
exchange,
ensuring
information
security
is
supreme
demand
for
storage
and
transmission.
Interlinking
cryptographic
techniques
with
steganographic
principles
can
enhance
confidentiality.
However,
there
have
been
no
reports
thus
far
to
develop
molecular
platforms
hybrid
crypto-steganography
systems.
Using
our
synthesized
nanoclusters
(BSA-Au/Ag
NCs)
through
bovine
serum
albumin
(BSA)
as
a
versatile
scaffold,
we
fabricated
platform
concatenated
logic
circuits
keypad
lock.
Then,
integrate
terrestrial
direction
transmission
navigation,
employing
double
block
cipher
by
combining
stego
key
shifting
system,
aimed
at
enhancing
paradigms.
Furthermore,
prioritize
protection
developing
an
enhanced
distress
call
protocol
using
polyalphabetic
activate
covert
communication
capabilities,
thereby
safeguarding
against
potential
infiltrators.
Chemical Society Reviews,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
review
focuses
on
stimuli-responsive
material
(SRM)-based
data
protection,
emphasizing
the
integration
of
intricate
logic
and
algorithms
in
SRM-constructed
hardware.
It
also
discusses
current
challenges
future
directions
field.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(26), P. 18041 - 18049
Published: June 20, 2024
Folding
thermodynamics,
quantitatively
described
using
parameters
such
as
ΔGfold°,
ΔHfold°,
and
ΔSfold°,
is
essential
for
characterizing
the
stability
functionality
of
noncanonical
nucleic
acid
structures
but
remains
difficult
to
measure
at
molecular
level.
Leveraging
programmability
dynamic
deoxyribonucleic
(DNA)
chemistry,
we
introduce
a
DNA-based
tool
capable
performing
free
energy
shift
assay
(FESA)
that
directly
characterizes
thermodynamics
DNA
in
their
native
environments.
FESA
operates
by
rational
design
reference
probe
energetically
equivalent
target
structure
series
toehold-exchange
reactions,
yet
structurally
incapable
folding.
As
result,
(ΔΔGrxn°)
observed
when
plotting
reaction
yield
against
each
toehold-exchange.
We
mathematically
demonstrated
ΔSfold°
analyte
can
be
calculated
based
on
ΔΔGrxn°.
After
validating
six
hairpins
comparing
measured
values
predictions
made
NUPACK
software,
adapted
characterize
structures,
encompassing
triplexes,
G-quadruplexes,
aptamers.
This
adaptation
enabled
successful
characterization
folding
these
complex
under
various
experimental
conditions.
The
development
marks
paradigm
technical
advancement
through
tools.
It
also
opens
new
avenues
probing
fundamental
chemical
biophysical
questions
lens
engineering
chemistry.