Communications Biology,
Journal Year:
2024,
Volume and Issue:
7(1)
Published: Nov. 14, 2024
The
sophisticated
envelope
of
Gram-negative
bacteria
modulates
the
uptake
small
molecules
in
a
side-chain-sensitive
manner.
Despite
intensive
theoretical
and
experimental
investigations,
general
set
pathways
underpinning
antibiotic
has
not
been
identified.
This
manuscript
discusses
passive
influx
versus
active
efflux
antibiotics,
considering
responsible
membrane
proteins
transported
molecules.
Recent
methods
have
analyzed
drug
transport
across
bacterial
order
to
understand
their
activity.
combination
vitro,
cellulo
silico
shed
light
on
key,
mainly
electrostatic,
interactions
between
molecule
surface,
porins
transporters
during
permeation.
A
key
factor
is
relationship
dose
an
compound
near
its
target
antibacterial
activity
critical
early
window.
Today,
methodology
breakthroughs
provide
fruitful
tools
precisely
dissect
transport,
identify
steps
resistance
associated
with
impermeability
efflux,
highlight
parameters
generate
more
effective
drugs.
controls
accumulation
via
mechanisms.
article
recent
cellulo,
highlighting
"drug-transporters"
dialogues
proposes
new
perspectives
overcome
resistance.
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(11)
Published: Jan. 30, 2023
Abstract
Osteomyelitis
is
a
destructive
disease
of
bone
tissue
caused
by
infection
with
pathogenic
microorganisms.
Because
the
complex
and
long‐term
abnormal
conditions,
osteomyelitis
one
refractory
diseases
in
orthopedics.
Currently,
anti‐infective
therapy
primary
modality
for
addition
to
thorough
surgical
debridement.
However,
bacterial
resistance
has
gradually
reduced
benefits
traditional
antibiotics,
development
advanced
antibacterial
agents
received
growing
attention.
This
review
introduces
main
targets
treating
osteomyelitis,
including
cell
wall,
membrane,
intracellular
macromolecules,
energy
metabolism,
focuses
on
their
mechanisms,
predicts
prospects
clinical
applications.
ACS Omega,
Journal Year:
2024,
Volume and Issue:
9(6), P. 6527 - 6536
Published: Feb. 1, 2024
Tissue
engineering
is
currently
one
of
the
fastest-growing
areas
engineering,
requiring
fabrication
advanced
and
multifunctional
materials
that
can
be
used
as
scaffolds
or
dressings
for
tissue
regeneration.
In
this
work,
we
report
a
bilayer
material
prepared
by
electrospinning
hybrid
poly(vinyl
alcohol)
(PVA)
bacterial
cellulose
(BC
NFs)
(top
layer)
over
highly
interconnected
porous
3D
gelatin-PVA
hydrogel
obtained
freeze-drying
process
(bottom
layer).
The
techniques
were
combined
to
produce
an
with
synergistic
effects
on
physical
biological
properties
two
materials.
was
characterized
using
Fourier
transform
infrared
spectroscopy
(FTIR),
scanning
electron
microscopy
(SEM),
water
contact
measurement
system
(WCMS).
Studies
swelling,
degradability,
porosity,
drug
release,
cellular
antibacterial
activities
performed
standardized
procedures
assays.
FTIR
confirmed
cross-linking
both
top
bottom
layers,
SEM
showed
structure
layer,
random
deposition
NFs
surface,
aligned
in
cross
section.
angle
(WCA)
hydrophilic
surface
material.
Swelling
analysis
high
degradation
good
stability.
released
Ag-sulfadiazine
sustained
controlled
manner
against
severe
disease-causing
gram
+
ive
−ive
(Escherichia
coli,
Staphylococcus
aureus,
Pseudomonas
aeruginosa)
strains.
vitro
studies
fibroblasts
(3T3)
human
embryonic
kidneys
(HEK-293),
which
desirable
cell
viability,
proliferation,
adhesion
bilayer.
Thus,
effect
resulted
potential
wound
dressing
healing
soft
engineering.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 20, 2024
Abstract
This
study
explores
the
coating
of
photocatalytic
nanoparticles
with
antimicrobial
peptides
(AMPs)
for
boosted
effects,
and
how
such
effects
depend
on
AMP
properties.
For
this,
TiO
2
are
coated
KYE21
or
its
hydrophobically
enhanced
variant
WWWKYE21.
Mirroring
free
peptides,
displayed
higher
binding
UV‐induced
degradation
bacteria‐like
than
mammalian‐like
membranes.
In
addition,
they
degraded
bacterial
lipopolysaccharides
(LPS).
WWWKYE21‐coated
to
LPS
membranes
degradation,
although
saturation
found
at
high
nanoparticle
binding.
Neutron
reflectometry
showed
that
peptide‐coated
resulted
in
partial
lipid
removal
absence
UV,
but
UV
illumination
caused
additional
featuring
increases
hydration
headgroup
acyl
chain
regions.
LPS,
induced
outer
O‐antigen
region.
Analogous
findings
model
systems,
against
Escherichia
coli
bacteria
pronounced,
while
toxicity
human
monocytes
remained
low.
Altogether,
results
show
boosts
without
causing
cell
toxicity.
From
a
broader
perspective,
points
potential
nanoarchitectonic
combination
component
properties
design
composite
NP
ACS Omega,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 14, 2025
The
lipid
matrix
of
the
outer
membrane
(OM)
Gram-negative
bacteria
consists
a
highly
asymmetric
bilayer
containing
phospholipids
on
inner
leaflet
and
lipopolysaccharides
(LPS)
in
layer.
latter
ensures
that
harmful
molecules
do
not
permeate
bacterial
cell,
but
polymyxin
B
(PmB),
last-resort
antibiotic,
is
capable
interfering
with
stability
LPS
layer
overcoming
OM
barrier.
We
have
previously
shown
efficacy
PmB
disrupting
isotopically
models
(2H-phospholipids
1H-LPS)
regulated
by
gel-to-fluid
phase
transition
Here,
we
employ
fully
deuterated
2H-LPS)
to
track
temperature-dependent
penetration
within
model
using
neutron
reflectometry.
use
model-independent
approach
quantify
as
function
both
concentration
temperature
well
model-dependent
analysis
localize
bilayer.
By
leveraging
ability
neutrons
differentiate
hydrogen
from
deuterium
structural
biology
find
hijacks
accumulates
predominantly
hydrophobic
region
A.
ECS Journal of Solid State Science and Technology,
Journal Year:
2024,
Volume and Issue:
13(4), P. 047002 - 047002
Published: April 1, 2024
Multidrug
resistance
(MDR)
is
a
significant
global
challenge
requiring
strategic
solutions
to
address
bacterial
infections.
Recent
advancements
in
nanotechnology,
particularly
the
synthesis
of
zinc
oxide
nanoparticles
(ZnO
NPs)
using
natural
agents
as
stabilizers
and
reducing
agents,
have
shown
promising
results
combating
MDR.
These
possess
strong
antimicrobial
properties
against
different
strains
Gram-positive
Gram-negative,
making
them
suitable
for
various
industries,
including
food,
pharmaceuticals,
coatings,
medical
devices.
ZnO-NPs
work
by
generating
reactive
oxygen
species,
releasing
ions
(Zn2+),
disrupting
cell
membrane,
interfering
with
metabolic
processes
genetic
material,
inducing
oxidative
stress
apoptosis.
However,
more
research
needed
refine
techniques,
control
size
morphology,
increase
antibacterial
efficacy.
To
fully
understand
their
potential,
interactions
proteins,
DNA,
walls
must
also
be
examined.
Investigating
synergistic
potential
biogenic
ZnO
NPs
conventional
treatments
could
enhance
therapeutic
effectiveness
while
minimizing
risk
emergence.
Here
we
provide
insight
into
bio
extracts
applications
well
factors
affecting
process
characterization
techniques
NPs.
studies
on
activity
pathogens
mechanisms
action
are
discussed.
Furthermore,
highlighted.
Frontiers in Microbiology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 3, 2024
The
increasing
threat
of
antibiotic
resistance
and
shrinking
treatment
options
for
infections
have
pushed
mankind
into
a
difficult
position.
looming
the
return
pre-antibiotic
era
has
caused
sense
urgency
to
protect
conserve
potency
therapy.
One
perverse
effects
is
dissemination
its
causative
agents
from
non-clinically
important
strains
clinically
vice
versa.
popular
saying
"Prevention
better
than
cure"
appropriate
tackling
resistance.
On
one
hand,
new
effective
antibiotics
are
required;
on
other
measures
use
antibiotics,
along
with
increased
awareness
in
general
public
related
use,
essential.
Awareness,
especially
resistance,
dissemination,
potential
threats,
can
help
greatly
controlling
abuse
containment
Antibiotic
drugs'
effectiveness
be
enhanced
by
producing
novel
analogs
or
adding
adjuvants
current
antibiotics.
Combinatorial
therapy
proven
successful
treating
multidrug-resistant
(MDR)
bacterial
infections.
This
review
aims
highlight
global
situation
discuss
methods
used
monitor,
prevent,
inhibit,
reverse
mechanisms
fight
against
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(7), P. 3927 - 3927
Published: March 31, 2024
Endotoxins
are
toxic
lipopolysaccharides
(LPSs),
extending
from
the
outer
membrane
of
Gram-negative
bacteria
and
notorious
for
their
toxicity
deleterious
effects.
The
comparison
different
LPSs,
isolated
various
bacteria,
shows
a
global
similar
architecture
corresponding
to
glycolipid
lipid
A
moiety,
core
oligosaccharide,
outermost
long
O-chain
polysaccharides
with
molecular
weights
2
20
kDa.
LPSs
display
high
diversity
specificity
among
genera
species,
each
bacterium
contains
unique
set
LPS
structures,
constituting
its
protective
external
barrier.
Some
not
due
particular
structures.
Different,
well-characterized,
highly
purified
were
used
in
this
work
determine
endotoxin
detection
rules
identify
impact
on
host.
Endotoxin
is
major
task
ensure
safety
human
health,
especially
pharma
food
sectors.
Here,
we
describe
structures
obtained
under
bacterial
growth
conditions
selective
methods
such
as
LAL,
HEK-blue
TLR-4,
LC-MS2,
MALDI-MS.
In
these
assays,
shown
respond
differently,
mainly
attributable
fatty
acid
numbers
chain
lengths,
presence
phosphate
groups,
possible
substitutions.
Journal of Chemical Theory and Computation,
Journal Year:
2024,
Volume and Issue:
20(15), P. 6890 - 6903
Published: July 15, 2024
Lipopolysaccharide
(LPS)
is
a
complex
glycolipid
molecule
that
the
main
lipidic
component
of
outer
leaflet
membrane
Gram-negative
bacteria.
It
has
very
limited
lateral
motion
compared
to
phospholipids,
which
are
more
ubiquitous
in
biological
membranes,
including
inner
The
slow-moving
nature
LPS
can
present
hurdle
for
molecular
dynamics
simulations,
given
(pragmatically)
accessible
timescales
simulations
currently
microseconds,
during
displays
some
conformational
but
hardly
any
diffusion.
Thus,
it
not
feasible
observe
phenomena
such
as
insertion
molecules,
antibiotics/antimicrobials,
directly
into
from
extracellular
side
nor
dissociating
proteins
via
using
available
models
at
atomistic
and
coarse-grained
levels
granularity.
Here,
we
model
deep
rough
compatible
with
Martini
2
force
field
scaled
down
nonbonded
interactions
enable
faster
We
show
faster-diffusing
able
reproduce
salient
biophysical
properties
standard
models,
due
its
motion,
molecules
penetrate
deeper
membranes
containing
model.
fast
ReLPS
experimentally
determined
patterns
interaction
while
also
allowing
associate
dissociate
within
microsecond
timescales.
complete
3
toolkit
Escherichia
coli
by
presenting
(standard)
this
field.