Nature Biotechnology,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 18, 2025
Abstract
Understanding
the
diverse
dynamic
behaviors
of
individual
RNA
molecules
in
single
cells
requires
visualizing
them
at
high
resolution
real
time.
However,
single-molecule
live-cell
imaging
unmodified
endogenous
has
not
yet
been
achieved
a
generalizable
manner.
Here,
we
present
fluorescence
situ
hybridization
(smLiveFISH),
robust
approach
that
combines
programmable
RNA-guided,
RNA-targeting
CRISPR–Csm
complex
with
multiplexed
guide
RNAs
for
direct
and
efficient
visualization
range
cell
types,
including
primary
cells.
Using
smLiveFISH,
track
native
NOTCH2
MAP1B
transcripts
living
identify
two
distinct
localization
mechanisms
cotranslational
translocation
mRNA
endoplasmic
reticulum
directional
transport
toward
periphery.
This
method
potential
to
unlock
principles
governing
spatiotemporal
organization
health
disease.
Laser & Photonics Review,
Год журнала:
2024,
Номер
18(11)
Опубликована: Июль 10, 2024
Abstract
Genetic
engineering
faces
persistent
challenges
in
achieving
precise
Deoxyribonucleic
acid
(DNA)
cleavage,
especially
with
the
limitations
associated
current
enzyme‐based
methods,
exemplified
by
issues
CRISPR
technologies.
This
study
introduces
a
groundbreaking
approach:
utilizing
reactive
oxygen
species
(ROS)
generated
Multiphoton
Absorption
(MPA)‐excited
Black
Phosphorus
Quantum
Dots
(BPQDs)
under
femto‐second
laser
irradiation.
innovative
method
not
only
allows
excitation
lower
energy
but
also
enhances
overall
efficiency.
The
integration
of
complementary
RNA
sequences
facilitates
high‐efficiency,
site‐selective
DNA
cleavage
system,
named
“TADPOLE”
(Targeted
Precision
Oriented
Laser
Excision).
Beyond
its
precision
targeting
arbitrary
using
quantum
dots,
TADPOLE
harnesses
unique
multiphoton
absorption
property
BPQDs,
enabling
lower‐energy
light
sources
suitable
for
vivo
applications
future.
Moreover,
approach
integrates
guiding
and
ultrafast
technology
to
provide
control
over
local
ROS
generation
minimal
heat
production.
guarantees
site‐specific
while
mitigating
risk
damage
non‐targeted
sequences.
In
summary,
this
catalyzes
advancements
enzyme‐free
technologies,
transformative
implications
genetic
engineering,
biotechnology,
medicine.
holistic
precision,
versatility,
endurance
presented
open
new
avenues
targeted
gene
therapies
related
fields.
Cell,
Год журнала:
2024,
Номер
187(13), С. 3249 - 3261.e14
Опубликована: Май 22, 2024
Thermostable
clustered
regularly
interspaced
short
palindromic
repeats
(CRISPR)
and
CRISPR-associated
(Cas9)
enzymes
could
improve
genome-editing
efficiency
delivery
due
to
extended
protein
lifetimes.
However,
initial
experimentation
demonstrated
Geobacillus
stearothermophilus
Cas9
(GeoCas9)
be
virtually
inactive
when
used
in
cultured
human
cells.
Laboratory-evolved
variants
of
GeoCas9
overcome
this
natural
limitation
by
acquiring
mutations
the
wedge
(WED)
domain
that
produce
>100-fold-higher
levels.
Cryoelectron
microscopy
(cryo-EM)
structures
wild-type
improved
(iGeoCas9)
reveal
contacts
between
WED
iGeoCas9
DNA
substrates.
Biochemical
analysis
shows
accelerates
unwinding
capture
substrates
under
magnesium-restricted
conditions
typical
mammalian
but
not
bacterial
These
findings
enabled
rational
engineering
other
orthologs
enhance
levels,
pointing
a
general
strategy
for
editing
enzyme
improvement.
Together,
these
results
uncover
new
role
demonstrate
how
accelerated
target
dramatically
improves
Cas9-induced
activity.
Journal of Chromatography A,
Год журнала:
2024,
Номер
1722, С. 464862 - 464862
Опубликована: Апрель 1, 2024
The
21st
century
has
been
particularly
productive
for
the
biopharmaceutical
industry,
with
introduction
of
several
classes
innovative
therapeutics,
such
as
monoclonal
antibodies
and
related
compounds,
gene
therapy
products,
RNA-based
modalities.
All
these
new
molecules
are
susceptible
to
aggregation
fragmentation,
which
necessitates
a
size
variant
analysis
their
comprehensive
characterization.
Size
exclusion
chromatography
(SEC)
is
one
reference
techniques
that
can
be
applied.
analytical
mAbs
now
well
established
some
them
emerging
newer
In
this
context,
objective
review
article
is:
i)
provide
short
historical
background
on
SEC,
ii)
suggest
clear
guidelines
selection
packing
material
mobile
phase
successful
method
development
in
modern
SEC;
iii)
highlight
recent
advances
use
narrow-bore
micro-bore
columns,
ultra-wide
pore
low-adsorption
column
hardware.
Some
important
innovations,
recycling
coupling
SEC
mass
spectrometry,
alternative
detectors
charge
detection
spectrometry
photometry
also
described.
addition,
discusses
multidimensional
setups
shows
most
at
preparative
scale.
third
part
article,
possibility
characterization
modalities
reviewed.
final
summary
opportunities
limitations
different
products.
Trends in Microbiology,
Год журнала:
2024,
Номер
32(12), С. 1229 - 1240
Опубликована: Июнь 5, 2024
Recent
studies
of
dynamic
interactions
between
epigenetic
modifications
a
host
organism
and
the
composition
or
activity
its
associated
gut
microbiota
suggest
an
opportunity
for
to
shape
microbiome
through
alterations
that
lead
changes
in
gene
expression
noncoding
RNA
activity.
We
use
insights
from
microbiota-induced
review
potential
epigenetically
regulate
microbiome,
which
bidirectional
'epigenome–microbiome
axis'
emerges.
This
axis
embeds
environmentally
induced
variation,
may
influence
adaptive
evolution
host–microbe
interactions.
furthermore
present
our
perspective
on
how
epigenome–microbiome
can
be
understood
investigated
within
holo-omic
framework
with
applications
applied
health
food
sciences.
Environmental Technology & Innovation,
Год журнала:
2024,
Номер
34, С. 103625 - 103625
Опубликована: Апрель 4, 2024
Contaminants,
such
as
nucleic
acids
or
toxic
small
molecules,
threaten
both
human
health
and
ecosystems
when
they
infiltrate
the
environment.
The
precise
highly
sensitive
identification
of
contaminants
holds
paramount
importance
across
diverse
domains,
including
safeguarding
food
integrity,
facilitating
clinical
diagnostics,
monitoring
environmental
conditions.
Traditional
methodologies,
encompassing
spectroscopy,
chromatography,
sequencing,
metagenomics,
have
conventionally
served
pivotal
roles
in
detection
processes.
Nevertheless,
these
methods
encountered
recurring
challenges
related
to
sensitivity,
specificity,
portability.
This
review
focuses
on
groundbreaking
CRISPR/Cas12-based
biosensors.
These
biosensors
leverage
incredible
precision
programmability
CRISPR/Cas
system
recognize
specific
targets.
Here,
we
comprehensively
assess
fundamental
mechanisms
that
enable
detection,
ranging
from
guide
RNA
design
collateral
cleavage.
versatility
CRISPR/Cas12
becomes
evident
through
their
applications.
applications
encompass
medical
safety,
monitoring.
transition
conventional
ultimately
represents
a
significant
milestone
contaminant
detection.
By
incorporating
molecular
biology,
nanotechnology,
bioinformatics,
potential
reshape
landscape
water
CRIPSR-Cas
diagnostics
is
transformative
technology
paves
way
for
safer
healthier
future
environment
life.
Nucleic Acids Research,
Год журнала:
2024,
Номер
52(4), С. e19 - e19
Опубликована: Янв. 5, 2024
Abstract
A
synthetic
biology
toolkit,
exploiting
clustered
regularly
interspaced
short
palindromic
repeats
(CRISPR)
and
modified
CRISPR-associated
protein
(Cas)
base-editors,
was
developed
for
genome
engineering
in
Gram-negative
bacteria.
Both
a
cytidine
base-editor
(CBE)
an
adenine
(ABE)
have
been
optimized
precise
single-nucleotide
modification
of
plasmid
targets.
CBE
comprises
deaminase
conjugated
to
Cas9
nickase
from
Streptococcus
pyogenes
(SpnCas9),
resulting
C→T
(or
G→A)
substitutions.
Conversely,
ABE
consists
fused
SpnCas9
A→G
T→C)
editing.
Several
nucleotide
substitutions
were
achieved
using
these
plasmid-borne
base-editing
systems
novel
protospacer
adjacent
motif
(PAM)-relaxed
(SpRY)
variant.
Base-editing
validated
Pseudomonas
putida
other
bacteria
by
inserting
premature
STOP
codons
into
target
genes,
thereby
inactivating
both
fluorescent
proteins
metabolic
(antibiotic-resistance)
functions.
The
functional
knockouts
obtained
via
reverted
the
wild-type
genotype
ABE.
Additionally,
series
induction-responsive
vectors
facilitate
curing
platform
single
cultivation
step,
simplifying
complex
strain
programs
without
relying
on
homologous
recombination
yielding
plasmid-free,
bacterial
cells.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Фев. 26, 2024
The
delivery
of
CRISPR
ribonucleoproteins
(RNPs)
for
genome
editing
in
vitro
and
vivo
has
important
advantages
over
other
methods,
including
reduced
off-target
immunogenic
effects.
However,
effective
RNPs
remains
challenging
certain
cell
types
due
to
low
efficiency
toxicity.
To
address
these
issues,
we
engineer
self-deliverable
that
can
promote
efficient
cellular
uptake
carry
out
robust
without
the
need
helper
materials
or
biomolecules.
Screening
cell-penetrating
peptides
(CPPs)
fused
CRISPR-Cas9
protein
identifies
potent
constructs
capable
neural
progenitor
cells.
Further
engineering
fusion
proteins
establishes
a
C-terminal
Cas9
with
three
copies
A22p,
peptide
derived
from
human
semaphorin-3a,
exhibits
substantially
improved
efficacy
compared
constructs.
We
find
generate
edits
clinically
relevant
genes
when
injected
directly
into
mouse
striatum.
Overall,
provide
facile
platform
vivo.
CRISPR/Cas-derived
base
editor
enables
precise
editing
of
target
sites
and
has
been
widely
used
for
basic
research
crop
genetic
improvement.
However,
the
efficiency
editors
at
different
targets
varies
greatly.
Plant Biotechnology Journal,
Год журнала:
2024,
Номер
22(5), С. 1198 - 1205
Опубликована: Фев. 27, 2024
Plants
have
evolved
a
multi-layered
immune
system
to
fight
off
pathogens.
However,
activation
is
costly
and
often
associated
with
growth
development
penalty.
In
crops,
yield
the
main
breeding
target
usually
affected
by
high
disease
resistance.
Therefore,
proper
balance
between
defence
critical
for
achieving
efficient
crop
improvement.
This
review
highlights
recent
advances
in
attempts
designed
alleviate
trade-offs
resistance
crops
mediated
(R)
genes,
susceptibility
(S)
genes
pleiotropic
genes.
We
also
provide
an
update
on
strategies
optimizing
growth-defence
breed
future
desirable
yield.