Abstract
Under
a
pH
value
lower
than
the
p
K
of
adenine
(3.5),
adenine‐rich
sequences
(A‐strand)
form
unique
parallel
A‐motif
duplex
due
to
protonation
A‐strand.
At
above
3.5,
deprotonation
adenines
leads
dissolution
A‐strand
single
coil.
This
pH‐reconfigurable
has
been
developed
as
novel
pH‐responsive
DNA
hydrogel,
termed
A‐hydrogel.
The
hydrogel
state
is
achieved
at
1.2
by
bridging
units,
which
are
cross‐linked
both
reverse
Hoogsteen
interaction
and
electrostatic
attraction.
Hydrogel‐to‐solution
transition
triggered
4.3
deprotonation‐induced
separation
duplex.
A‐hydrogel
system
undergoes
reversible
hydrogel–solution
transitions
subjecting
cyclic
shifts
between
4.3.
An
anti‐inflammatory
medicine,
sulfasalazine
(SSZ),
intercalates
into
duplex,
loaded
Its
pH‐controlled
release
from
successfully
demonstrated.
strong
acid‐induced
may
fill
gap
that
other
mild
acid‐responsive
hydrogels
cannot
do,
such
protection
orally
delivered
drug
in
hostile
stomach
environment
against
acid
(pH
~
1.2)
digestive
enzymes.
Abstract
Deoxyribonucleic
acid
(DNA),
a
fundamental
biomacromolecule
in
living
organisms,
serves
as
the
carrier
of
genetic
information.
Beyond
its
role
encoding
biological
functions,
DNA's
inherent
ability
to
hybridize
through
base
pairing
has
opened
new
avenues
for
application
sciences.
This
review
introduces
DNA
nanotechnology
and
DNA‐encoded
library
(DEL),
highlights
their
shared
design
principles
related
assembly.
First,
foundational
overview
structural
nanotechnology,
including
strategies
historical
development
is
provided.
Subsequently,
various
approaches
are
examined
dynamic
from
strand
displacement
reactions
DNA‐templated
polymer
synthesis.
Second,
how
principle
assembly
facilitated
diverse
formats
self‐assembly‐based
DEL
synthesis,
DNA‐template
(DTS),
template‐mediated
proximity
induction
effects
examined.
These
advancements
all
underpinned
by
unique
property
Finally,
this
summarizes
common
terms
methodology
design.
Additionally,
potential
synergies
explored
between
these
two
technologies,
envisioning
future
applications
where
they
can
be
combined
create
more
versatile
exquisite
functionalities.
JACS Au,
Год журнала:
2025,
Номер
5(2), С. 550 - 570
Опубликована: Фев. 6, 2025
Cell
surface
engineering
is
a
rapidly
advancing
field,
pivotal
for
understanding
cellular
physiology
and
driving
innovations
in
biomedical
applications.
In
this
regard,
DNA
nanotechnology
offers
unprecedented
potential
precisely
manipulating
functionalizing
cell
surfaces
by
virtue
of
its
inherent
programmability
versatile
functionalities.
Herein,
Perspective
provides
comprehensive
overview
emerging
trends
engineering,
focusing
on
key
nanostructure-based
tools,
their
roles
regulating
physiological
processes,
We
first
discuss
the
strategies
integrating
molecules
onto
surfaces,
including
attachment
oligonucleotides
higher-order
nanostructure.
Second,
we
summarize
impact
DNA-based
various
such
as
membrane
protein
degradation,
signaling
transduction,
intercellular
communication,
construction
artificial
components.
Third,
highlight
applications
DNA-engineered
targeted
therapies
cancer
inflammation,
well
capture/protection
diagnostic
detection.
Finally,
address
challenges
future
directions
nanotechnology-based
engineering.
This
aims
to
provide
valuable
insights
rational
design
contributing
development
precise
personalized
medicine.
Advanced Functional Materials,
Год журнала:
2022,
Номер
32(46)
Опубликована: Сен. 2, 2022
Abstract
Naturally
occurring
micro/nanoparticles
provide
an
incredible
array
of
potential
sources
when
preparing
hybrid
micro/nanorobots
and
their
intrinsic
properties
can
be
exploited
as
multitasking
functionalities
modern
robotics
well
ensuring
mass
production
availability.
Herein,
magnetic
biological
bots
(BioBots)
prepared
from
defatted
sunflower
pollen
microparticles
by
ferromagnetic
metal
layer
evaporation
on
one
side
its
surface
are
described.
It
is
demonstrated
that
the
methodology
employed
introduces
to
microparticles‐based
BioBots
enable
actuation.
Interestingly,
as‐prepared
pollen‐based
naturally
attract
cancer
cells
due
opposite
charges
(positive
negative,
respectively).
Such
attracted
then
transported
microrobots.
This
strong
attraction
also
allows
delivery
drugs
intended
kill
cells.
Sunflower‐based
fabricated
in
large
quantities,
programmable,
making
them
promising
candidates
for
cell
therapy.
Bioactive Materials,
Год журнала:
2023,
Номер
28, С. 50 - 60
Опубликована: Май 12, 2023
As
the
most
abundant
liver-specific
microRNA,
microRNA-122
(miR122)
played
a
crucial
role
in
differentiation
of
stem
cells
into
hepatocytes.
However,
highly
efficient
miR122
delivery
still
confronts
challenges
including
poor
cellular
uptake
and
easy
biodegradation.
Herein,
we
for
first
time
demonstrated
that
tetrahedral
DNA
(TDN)
nanoplatform
had
great
potential
inducing
human
mesenchymal
(hMSCs)
functional
hepatocyte-like
(HLCs)
by
transferring
to
hMSCs
efficiently
without
any
extrinsic
factors.
compared
with
miR122,
miR122-functionalized
TDN
(TDN-miR122)
could
significantly
up-regulate
protein
expression
levels
mature
hepatocyte
markers
hepatocyte-specific
marker
genes
hMSCs,
indicating
TDN-miR122
particularly
activate
properties
developing
cell-based
therapies
vitro.
The
transcriptomic
analysis
further
indicated
mechanism
assisted
differentiated
HLCs.
TDN-miR122-hMSCs
exhibited
hepatic
cell
morphology
phenotype,
up-regulated
specific
biofunctions
comparison
undifferentiated
MSCs.
Preclinical
vivo
transplantation
appeared
combination
or
rescue
acute
liver
failure
injury
through
function
supplement,
anti-apoptosis,
proliferation
promotion,
anti-inflammatory.
Collectively,
our
findings
may
provide
new
facile
approach
therapy.
Further
large
animal
model
explorations
are
needed
study
their
clinical
translation
future.
Abstract
Under
a
pH
value
lower
than
the
p
K
of
adenine
(3.5),
adenine‐rich
sequences
(A‐strand)
form
unique
parallel
A‐motif
duplex
due
to
protonation
A‐strand.
At
above
3.5,
deprotonation
adenines
leads
dissolution
A‐strand
single
coil.
This
pH‐reconfigurable
has
been
developed
as
novel
pH‐responsive
DNA
hydrogel,
termed
A‐hydrogel.
The
hydrogel
state
is
achieved
at
1.2
by
bridging
units,
which
are
cross‐linked
both
reverse
Hoogsteen
interaction
and
electrostatic
attraction.
Hydrogel‐to‐solution
transition
triggered
4.3
deprotonation‐induced
separation
duplex.
A‐hydrogel
system
undergoes
reversible
hydrogel–solution
transitions
subjecting
cyclic
shifts
between
4.3.
An
anti‐inflammatory
medicine,
sulfasalazine
(SSZ),
intercalates
into
duplex,
loaded
Its
pH‐controlled
release
from
successfully
demonstrated.
strong
acid‐induced
may
fill
gap
that
other
mild
acid‐responsive
hydrogels
cannot
do,
such
protection
orally
delivered
drug
in
hostile
stomach
environment
against
acid
(pH
~
1.2)
digestive
enzymes.