A Dual-Capture and Dual-Output 3D DNA Walker System Integrated with Ligases Enables Ultrasensitive Detection of Single-Nucleotide Polymorphisms
Yunshan Zhang,
No information about this author
Qianglong Tan,
No information about this author
Fang Yang
No information about this author
et al.
Analytical Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
DNA
walkers,
as
structurally
and
functionally
programmable
signal
amplification
tools,
exhibit
great
potential
for
application
in
the
field
of
biosensing.
Traditional
walkers
often
rely
on
enzymes
operation,
posing
compatibility
challenges,
while
handful
existing
enzyme-free
demonstrate
limited
performance.
To
address
this,
we
innovatively
developed
an
efficient
3D
walker
with
dual
capture
output
capabilities.
Coupled
ligase
chain
reaction
(LCR),
this
system
facilitates
highly
sensitive
specific
detection
single
nucleotide
polymorphisms
(SNPs).
Specifically,
LCR
precisely
identifies
single-base
mutations,
effectively
transmitting
biological
information.
The
is
based
entropy-driven
circuit
cycling
technology.
In
system,
products
serve
driving
strands
walker,
independently
binding
to
track
walking
legs
immobilized
gold
nanoparticles,
forming
a
unique
mechanism.
Each
strand
carries
two
chains,
significantly
enhancing
efficiency.
Benefiting
from
novel
strategy,
our
biosensing
exhibits
exceptional
sensitivity
mutant
targets
(MT),
detecting
MT
at
concentrations
low
30.3
aM
distinguishing
heterozygous
samples
0.01%
mutation
frequency.
Furthermore,
has
been
successfully
applied
genotyping
abundance
assessment
genomes
fresh
soybean
leaves,
demonstrating
its
vast
practical
applications.
summary,
research
pioneers
capabilities,
develops
ultrasensitive
tool.
This
provides
strong
technical
support
advancement
genetic
research.
Language: Английский
From Leaf to Lab-on-Cloth: Spatial DNA Nanorobotics and 2D Graphyne Synergy Enable Ultra-Precise Electrochemical Tracking of Sugarcane Pokkah Boeng Disease
Qingnian Wu,
No information about this author
Yu Ya,
No information about this author
Changwen Jin
No information about this author
et al.
Biosensors and Bioelectronics,
Journal Year:
2025,
Volume and Issue:
283, P. 117548 - 117548
Published: May 2, 2025
Language: Английский
Investigation of the DNA Methylation-Modified 8–17 DNAzyme Functions via Sensitive Catalytic Hairpin Self-Assembly Reaction
Wanxue Wang,
No information about this author
Guoying Li,
No information about this author
Xinghui Zhou
No information about this author
et al.
ACS Sensors,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 19, 2025
8-17
DNAzyme
is
a
well-known
versatile
nucleic
acid
tool
for
achieving
specific
cleavage
function,
and
thus,
investigation
of
functions
can
prove
to
be
great
significance.
The
conventional
epigenetic
modification
on
may
pave
new
way
the
study
catalytic
properties.
Herein,
most
abundant
best
characterized
modifications
5-methylcytosine
(5mC)
N6-methyladenosine
(m6A)
are
introduced
into
central
core
stem
sequence
evaluate
activity.
modified
DNAzymes
arranged
recognize
cleave
single-stranded
DNA
(ssDNA)
substrates
that
contain
5'-rAG-3'
motif,
producing
large
numbers
short
ssDNA
leaving
different
amounts
undegraded
because
their
disparate
excision
efficiency.
Meanwhile,
used
as
triggering
hairpin
self-assembly
(CHA)
reaction.
Benefiting
from
facile
sensitive
CHA
reaction,
methylation-induced
fluctuations
activity
directly
amplified
detected.
Moreover,
dioxygenase
ten-eleven
translocation
protein
2
(Tet
2)
offers
possibility
exploring
reversibility
methylation-modified
through
demethylation
process.
In
this
study,
we
found
both
5mC
m6A
in
circular
might
lead
significant
inhibition
effect
DNAzyme.
However,
little
variation
was
observed
when
region
labeled
with
5mC.
Additionally,
alkaline
condition
(pH
=
9.5)
enabled
partial
recovery
DNAzyme-19-5mC
(∼52.9%).
More
impressively,
these
were
employed
regulation
miRNA-21
level
nonsmall
cell
lung
cancer
(A549)
cells
human
cervical
(HeLa)
cells,
revealing
decrease
intracellular
content
showed
positive
correlation
death
tested
cells.
This
would
hopefully
advance
epigenetics
research
dramatically
expand
biosensing
application
DNAzymes.
Language: Английский