Dual-atom
nanozymes
(DAzymes)
have
garnered
considerable
attention
as
catalysts
for
reactive
oxygen
species
(ROS)-based
therapies,
effectively
leveraging
ROS
generation
within
the
tumor
microenvironment
(TME).
Herein,
we
introduce
FeMn-NCe
DAzymes,
which
are
meticulously
engineered
enhanced
peroxidase
(POD)-mimetic
activity
and
potent
radiosensitization
to
advance
radioimmunotherapy.
Density
functional
theory
(DFT)
calculations
reveal
that
DAzymes
lower
energy
barrier
increase
substrate
affinity,
enabling
highly
efficient
catalytic
performance.
Within
TME,
these
efficiently
convert
overexpressed
hydrogen
peroxide
(H2O2)
into
hydroxyl
radicals
(•OH),
potentially
activating
cGAS-STING
immune
pathway.
This
POD-mimetic
catalysis
is
further
accelerated
under
X-ray
irradiation,
significantly
enhancing
radiosensitization.
Additionally,
a
uniform
coating
of
ultrasmall
gold
nanoparticles
on
enhances
absorption
cancer
cells.
The
incorporation
STING
agonist
diABZI
onto
induces
long-term
antitumor
immunity,
reprograms
immunosuppressive
suppresses
growth
metastasis
following
single
low-dose
treatment.
work
highlights
valuable
strategy
designing
radiodynamic
immunotherapy.
Angewandte Chemie,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 12, 2025
Abstract
Nanozymes
with
atomically
dispersed
metal
sites
(ADzymes),
especially
single‐atom
nanozymes,
have
attracted
widespread
attention
in
recent
years
due
to
their
unique
advantages
mimicking
the
active
of
natural
enzymes.
These
nanozymes
not
only
maximize
exposure
catalytic
but
also
possess
superior
activity
performance,
achieving
challenging
reactions.
position
ADzymes
as
highly
promising
candidates
field
sensing
and
biosensing.
This
review
summarizes
classification
properties
ADzymes,
systematically
highlighting
some
typical
regulation
strategies
involving
central
metal,
coordination
environment,
etc.,
achieve
catalytical
activity,
specificity,
multifunctionality.
Then,
we
present
advances
different
fields,
including
colorimetry,
fluorescence,
electrochemistry,
chemiluminescence,
photoelectrochemistry,
electrochemiluminescence.
Taking
advantage
resultant
show
great
potential
goal
sensitivity,
selectivity
accuracy
for
detection
various
targets.
Specifically,
underlying
mechanisms
terms
signal
amplification
were
discussed
detail.
Finally,
current
challenges
perspectives
on
development
advanced
are
discussed.
Angewandte Chemie International Edition,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 12, 2025
Abstract
Nanozymes
with
atomically
dispersed
metal
sites
(ADzymes),
especially
single‐atom
nanozymes,
have
attracted
widespread
attention
in
recent
years
due
to
their
unique
advantages
mimicking
the
active
of
natural
enzymes.
These
nanozymes
not
only
maximize
exposure
catalytic
but
also
possess
superior
activity
performance,
achieving
challenging
reactions.
position
ADzymes
as
highly
promising
candidates
field
sensing
and
biosensing.
This
review
summarizes
classification
properties
ADzymes,
systematically
highlighting
some
typical
regulation
strategies
involving
central
metal,
coordination
environment,
etc.,
achieve
catalytical
activity,
specificity,
multifunctionality.
Then,
we
present
advances
different
fields,
including
colorimetry,
fluorescence,
electrochemistry,
chemiluminescence,
photoelectrochemistry,
electrochemiluminescence.
Taking
advantage
resultant
show
great
potential
goal
sensitivity,
selectivity
accuracy
for
detection
various
targets.
Specifically,
underlying
mechanisms
terms
signal
amplification
were
discussed
detail.
Finally,
current
challenges
perspectives
on
development
advanced
are
discussed.
Dual-atom
nanozymes
(DAzymes)
have
garnered
considerable
attention
as
catalysts
for
reactive
oxygen
species
(ROS)-based
therapies,
effectively
leveraging
ROS
generation
within
the
tumor
microenvironment
(TME).
Herein,
we
introduce
FeMn-NCe
DAzymes,
which
are
meticulously
engineered
enhanced
peroxidase
(POD)-mimetic
activity
and
potent
radiosensitization
to
advance
radioimmunotherapy.
Density
functional
theory
(DFT)
calculations
reveal
that
DAzymes
lower
energy
barrier
increase
substrate
affinity,
enabling
highly
efficient
catalytic
performance.
Within
TME,
these
efficiently
convert
overexpressed
hydrogen
peroxide
(H2O2)
into
hydroxyl
radicals
(•OH),
potentially
activating
cGAS-STING
immune
pathway.
This
POD-mimetic
catalysis
is
further
accelerated
under
X-ray
irradiation,
significantly
enhancing
radiosensitization.
Additionally,
a
uniform
coating
of
ultrasmall
gold
nanoparticles
on
enhances
absorption
cancer
cells.
The
incorporation
STING
agonist
diABZI
onto
induces
long-term
antitumor
immunity,
reprograms
immunosuppressive
suppresses
growth
metastasis
following
single
low-dose
treatment.
work
highlights
valuable
strategy
designing
radiodynamic
immunotherapy.