Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 3, 2024
Abstract
Since
the
diseases
that
cause
bone
defects
are
mostly
inflammatory
diseases,
current
grafts
unable
to
effectively
regulate
osteoimmune
activity,
leading
impaired
osteogenesis
and
unfavorable
regeneration.
In
this
study,
inspired
by
composition,
biomimetic
mesoporous
bioactive
glass
nanoparticle
(MBG)/bovine
serum
albumin
(BSA)
designed
for
defects.
Systematically,
MBG/BSA
evaluated
characterization,
bioactivity,
anti‐inflammatory,
antioxidant
osteogenic
activity.
proved
be
biocompatible
can
release
ions
including
calcium
silicon
in
a
sustained
manner.
Furthermore,
reprograms
macrophage
phenotype
toward
anti‐inflammation
is
beneficial
The
antioxidative
activity
also
validated
under
inflammation
mechanism
may
via
interleukin‐4
(IL‐4)/Signal
transducer
activator
of
transcription
6
(STAT6)
pathway.
differentiation
mineralization
facilitated
due
improved
immunoregulation
MBG/BSA.
Overall,
work
suggests
with
immunomodulatory
properties
an
ideal
material
regeneration
application.
Soft Matter,
Journal Year:
2025,
Volume and Issue:
21(10), P. 1781 - 1812
Published: Jan. 1, 2025
Peptide-mediated
liquid–liquid
phase
separation
(LLPS)
underpins
the
formation
of
dynamic
biomolecular
condensates,
regulated
by
diverse
molecular
interactions,
and
highlights
potential
applications
in
drug
delivery
synthetic
biology.
ACS Sensors,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
High-fidelity
tracking
of
glycogen
dynamics
in
living
biosystems
is
critical
for
exploring
the
biological
role
metabolism
diseases.
However,
situ
information
on
state
mainly
relies
a
glucose
uptake
fluorescence
probe
2-NBDG,
which
has
proven
to
be
extremely
limited
owing
"always-on"
fluorescence,
short
emission
wavelength,
and
low
signal-to-noise
(S/N)
ratio.
Herein,
we
first
time
demonstrate
metabolic-activated
off-on
through
covalently
attaching
molecular
rotor
with
hydrophilic
at
C-2
position
guarantee
good
miscibility
complete
fluorescence-off
before
metabolic
incorporation
into
particles.
The
Glycogen-Red
achieves
negligible
background
(1/30
times
than
2-NBDG)
an
ultrahigh
S/N
ratio
(61-fold
lighting-up
near-infrared
(NIR)
biosynthesis.
Notably,
our
unique
characteristic
bypassing
washing
steps,
offering
powerful
toolbox
real-time
biosynthesis
super-resolution
mapping
structures
cells.
Short
phase-separating
peptides
serve
as
liquid-based
vehicles
due
to
their
remarkable
fluidity
and
cell
permeability,
holding
great
promise
in
diffusion-limited
applications
such
intracellular
drug
delivery
or
penetration
into
deep-seated
tumors.
However,
tuning
the
phase
stability
phase-transition
sensitivity
of
these
coacervates
response
specific
pathological
signals
remains
a
significant
challenge.
To
tackle
this
challenge,
study
presents
peptide/hyaluronic
acid
(HA)
complex
coacervate
system,
which
undergoes
solid-to-coacervate
transition
upon
exposure
matrix
metalloproteinase
9
(MMP-9).
By
harnessing
disease-relevant
enzyme,
overexpressed
ovarian
tumor
microenvironment,
we
further
demonstrate
improved
infiltration
Hey
cells
spheroids.
These
observations
highlight
feasibility
modulating
behaviors
advanced
functions
through
sequence-specific
monomer
design,
offering
practical
strategy
for
on-target
medicine
The Journal of Physical Chemistry Letters,
Journal Year:
2025,
Volume and Issue:
unknown, P. 3553 - 3561
Published: March 31, 2025
Liquid–liquid
phase
separation
(LLPS)
of
biomolecules
is
a
fundamental
cellular
process
that
essential
for
maintaining
homeostasis
and
facilitating
biochemical
activities.
On
the
other
hand,
aberrant
alters
condensate
fluidity
causes
transition
from
liquid-like
condensates
to
solid-like
condensates,
which
may
lead
formation
pathological
aggregations
often
observed
in
neurodegenerative
diseases.
Condensate
usually
assessed
by
fluorescence
recovery
after
photobleaching.
Here,
we
reveal
lifetimes
several
fluorescent
proteins
are
sensitive
LLPS
liquid-to-solid
transition.
Furthermore,
identify
key
residues
regulate
sensitivity
toward
separation.
Thus,
apply
lifetime
imaging
microscopy
(FLIM)
visualize
living
cells,
demonstrating
FLIM
nondestructive
method
tracking
changes
real
time.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 22, 2025
Polypeptide-based
liquid-liquid
phase
separation
(LLPS)
has
received
considerable
attention
as
it
governs
the
formation
of
membraneless
organelles
in
cells.
However,
detailed
mechanistic
understanding
how
one
most
prevalent
cationic
amino
acids
proteins,
arginine,
interacts
with
various
biomolecules
to
induce
and
undergo
morphogenesis
remains
be
resolved.
Herein,
we
report
behavior
transformation
arginine-rich
coacervates
into
vesicular
structures
upon
introducing
polyphosphates.
Transformation
vesicles
was
shown
occur
independent
initial
anionic
counterparts
driven
by
salt-bridge
interactions
between
guanidinium
groups
arginine
residues
phosphates.
We
also
investigate
role
intermolecular
forces
ionic
effects
on
morphological
further
exploit
their
potential
assembly
artificial
tissue-like
constructs.
Overall,
our
findings
underpin
a
unifying
principle
for
vesicle
from
potency
reconstituting
hierarchical
biological
microcompartments.
Biomolecular
coacervates,
dynamic
compartments
formed
via
liquid-liquid
phase
separation
(LLPS),
are
essential
for
orchestrating
intracellular
processes
and
have
emerged
as
versatile
tools
in
bioengineering.
Peptides,
with
their
modular
amino
acid
sequences,
exhibit
unique
potential
coacervate
design
due
to
ability
undergo
LLPS
while
offering
precise
control
over
molecular
architecture
environmental
responsiveness.
Their
simplicity,
synthetic
accessibility,
tunability
make
peptide-based
coacervates
particularly
attractive
biomedical
materials
applications.
However,
the
formation
stability
of
these
systems
depend
on
a
delicate
balance
intrinsic
factors
(e.g.,
sequence
charge,
hydrophobicity,
chain
length)
extrinsic
conditions
pH,
ionic
strength,
temperature),
necessitating
deeper
understanding
interplay.
This
review
synthesizes
recent
advances
mechanisms
driving
peptide
coacervation,
emphasizing
how
cues
govern
behavior.
We
further
highlight
groundbreaking
applications,
from
drug
delivery
platforms
protocell
mimics,
discuss
strategies
translate
mechanistic
insights
into
functional
materials.
By
bridging
fundamental
principles
innovative
this
work
aims
accelerate
development
programmable,
multifunctional
systems,
roadmap
next-generation
biochemical
technologies.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 25, 2025
Amyloid-β
(Aβ)
peptides
exhibit
distinct
biological
activities
across
multiple
physical
length
scales,
including
monomers,
oligomers,
and
fibrils.
The
transition
from
Aβ
monomers
to
pathological
aggregates
correlates
with
the
emergence
of
chemical
toxicity,
which
plays
a
critical
role
in
progression
neurodegenerative
disorders.
However,
relationship
between
state
assemblies
their
toxicity
remains
poorly
understood.
Here,
we
show
that
can
spontaneously
generate
reactive
oxygen
species
(ROS)
through
transition-state-specific
inherent
nonenzymatic
redox
activity.
During
initial
intermediate
oligomers
or
condensates
final
fibrils,
interfacial
electrochemical
environments
emerge
vary
at
liquid–liquid
liquid–solid
interfaces.
Determined
by
vibrational
Stark
effect
using
electronic
pre-resonance
stimulated
Raman
scattering
microscopy,
field
such
is
on
order
10
MV/cm.
Interfacial
activity,
depends
state,
modulate
spontaneous
oxidation
hydroxide
anions,
leads
formation
hydroxyl
radicals.
Interestingly,
this
activity
modifies
composition
establishes
self-regulated
positive
feedback
loop
accelerates
aggregation
promotes
fibril
formation,
represents
new
functioning
mechanism
beyond
cross-linking.
Leveraging
mechanistic
insight,
identified
small
molecules
capable
disrupting
scavenging
radicals
perturbing
interface,
thereby
inhibiting
formation.
Our
findings
provide
model
neurotoxicity
reveal
interfaces
modulating
dynamics
biomolecular
assemblies.
These
results
offer
novel
framework
for
therapeutic
intervention
Alzheimer's
disease
related
Fluid
protein
condensates
are
used
as
precursor
phases
for
fabricating
extracellular
protein-based
materials
including
elastin,
spider
silk,
and
mussel
byssus.
The
byssus,
utilized
by
mussels
anchoring
in
marine
environments,
consists
of
tough,
self-healing
adhesive
fibers.
Byssus
formation
involves
the
secretion
condensate
droplets
under
acidic
conditions
that
subsequently
solidify
basic
seawater
conditions.
We
currently
have
a
poor
understanding
physicochemical
triggers
molecular-level
interactions
at
play,
particular
role
pH
sulfate
anions
previously
identified
during
native
fabrication.
Here,
we
investigated
sulfate-dependent
structural
mechanical
response
made
from
recombinant
byssus
(mfp-1)
using
optical
tweezers
microrheology,
FRAP,
confocal
Raman
spectroscopy,
NMR,
cryo-EM.
found
concentration
increased,
viscoelastic
became
more
rigid
presence
ions
compared
with
chloride
ions,
consistent
spectroscopic
analysis
indicating
different
molecular
these
chemical
These
studies
highlight
crucial
interplay
between
tuning
viscoelasticity
via
control
intermolecular
interactions,
providing
insights
into
natural
process
relevance
bio-inspired
processing
sustainable
plastics
tissue
engineering.