The Journal of Physical Chemistry B,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 7, 2025
As
one
of
nature's
most
fundamental
blueprints
and
due
to
its
critical
role
in
life
processes,
DNA
has
naturally
become
the
cornerstone
numerous
research
efforts.
One
particularly
intriguing
area
study
is
understanding
how
small
molecules
interact
with
nucleic
acids.
In
this
study,
we
investigated
interaction
between
plant-derived
indole
alkaloid
Raubasine
(Ajmalicine;
AJM)
Salmon
Testes
(ST)
using
biophysical
computational
techniques.
A
hyperchromic
shift
fluorescence
intensity
indicated
effective
binding
AJM
ST
DNA.
The
constant
was
order
105
M–1
a
single
preferential
mode.
Thermodynamic
analysis
revealed
that
exothermic
driven
by
positive
entropy
negative
enthalpy.
salt-dependent
indicates
involvement
nonpolyelectrolytic
forces
interaction.
Studies
iodide
quenching,
urea
denaturation,
dye
displacement,
molecular
docking
further
support
binds
through
groove
binding.
Structural
perturbation
evident
from
circular
dichroism.
stability
AJM–DNA
complex
confirmed
dynamics
simulations.
Prolonged
elevated
blood
glucose
levels
induce
nonenzymatic
glycation
DNA,
resulting
DNA–AGE
(advanced
end-products)
formation
free
radical
production,
which
disrupts
structure.
We
explored
ST-DNA
suppression
AJM.
DNA–AGEs
vitro
were
characterized
UV–vis
spectroscopy.
inhibition
assessed
changes
AGEs
intensity,
gel
electrophoresis
patterns,
antioxidant
activity,
highlighting
ability
target
glycated
sites
or
neutralize
radicals
generated
during
glycation.
Our
findings
reveal
AJM's
potential
prevent
AGEs,
may
offer
promising
avenues
for
targeted
therapies
against
glycation-related
diseases
such
as
diabetes,
neurodegeneration,
cancer.
The Journal of Physical Chemistry B,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 5, 2025
Lobeline
(LOB)
is
a
bioactive
alkaloid
known
for
its
neuroprotective
and
cognitive-enhancing
properties,
particularly
in
mitigating
oxidative
stress
inflammation
associated
with
neurodegenerative
diseases.
While
LOB
has
been
studied
pharmacological
roles
CNS
disorders,
substance
abuse
treatment,
smoking
cessation,
molecular
interactions
proteins
potential
antiamyloid,
antiglycation,
antioxidant
properties
remain
largely
unexplored.
This
study
addresses
this
gap
by
analyzing
ovalbumin
(OVA)
through
advanced
biophysical
computational
techniques
to
elucidate
therapeutic
inform
drug
development.
Fluorescence
spectroscopy
confirmed
static
quenching
mechanism
binding
constant
(Kb)
of
105
M-1
monopreferential
site
OVA
LOB.
Isothermal
titration
calorimetry
(ITC)
indicated
an
exothermic,
entropy-driven
interaction,
while
differential
scanning
(DSC)
demonstrated
LOB-induced
stabilization
OVA.
Synchronous
fluorescence
red
edge
excitation
shift
highlighted
LOB's
effect
on
Trp
Tyr
residues,
circular
dichroism
(CD)
conformational
changes
Molecular
modeling
(docking
dynamic
simulation)
corroborated
the
experimental
findings.
Turbidity,
thioflavin
T
(ThT),
nile
(NR),
8-anilinonaphthalene-1-sulfonic
acid
(ANS),
CD,
morphological
studies
fibril
formation,
aggregation
was
shown
be
inhibited
ligand
vitro.
Additionally,
d-fructose
used
glycate
protein,
creating
model
examine
antiglycation
effects
These
aspects
are
essential
advancing
targeted
design
delivery
systems,
as
they
provide
vital
insights
into
modern
biochemical
research.
ACS Applied Bio Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 18, 2024
Oligomers
and
amyloid
fibrils
formed
at
different
stages
of
protein
aggregation
are
important
biomarkers
for
a
variety
neurodegenerative
diseases
including
Alzheimer's
Parkinson's
diseases.
The
development
probes
the
sensitive
detection
oligomeric
species
is
early
stage
diagnosis
amyloidogenic
Many
small
molecular
dyes
have
been
developed
to
probe
dynamic
growth
fibrils.
However,
there
lack
discriminatory
strategies
monitor
dynamics
both
oligomers
based
on
differential
modulation
photophysical
properties
single
dye.
Here
we
report
pyrene-based
intramolecular
charge
transfer
(ICT)
dye
with
large
Stokes
shifted
red-emitting
induced
emission
(AIE)
monitoring
populations
during
hen
egg
white
lysozyme
(HEWL)
protein.
At
aggregation,
accumulation
HEWL
results
in
rapid
substantial
increase
red
AIE
intensity
660
nm.
Later,
as
transform
into
mature
fibrils,
exhibits
distinct
change.
Binding
strongly
suppresses
enhances
ICT
emission.
This
evidenced
by
gradual
decrease
(∼660
nm)
an
LE
(∼490
(∼540
intensities
later
aggregation.
Thus,
provides
simultaneous
measurements
population
also
enables
imaging
simultaneously
using
channels
super-resolution
confocal
fluorescence
microscopy.
The Journal of Physical Chemistry B,
Journal Year:
2024,
Volume and Issue:
128(18), P. 4283 - 4300
Published: April 29, 2024
Kidney-associated
human
lysozyme
amyloidosis
leads
to
renal
impairments;thus,
patients
are
often
prescribed
furosemide.
Based
on
this
fact,
the
effect
of
furosemide
induced
fibrillation,
in
vitro,
is
evaluated
by
spectroscopic,
calorimetric,
computational,
and
cellular-based
assays/methods.
Results
show
that
increases
lag
phase
decreases
apparent
rate
aggregation
lysozyme,
thereby
decelerating
nucleation
amyloid
fibril
formation,
as
confirmed
decrease
level
Thioflavin-T
fluorescence.
Fewer
entities
hydrodynamic
radii
∼171
nm
instead
fibrils
(∼412
nm)
detected
presence
dynamic
light
scattering.
Moreover,
extent
conversion
α/β
structure
into
a
predominant
β-sheet.
The
isothermal
titration
calorimetry
established
forms
complex
with
which
was
also
through
fluorescence
quenching
computational
studies.
Also,
lytic
activity
inhibited
competitively
due
involvement
amino
acid
residues
active
site
catalysis,
well
formation.
Conclusively,
interacts
Gln58,
Ile59,
Asn60,
Ala108,
Trp109
aggregation-prone
regions
2
4
masking
its
sites
generating
only
lower-order
less
toxic
red
blood
cells
than
fibrils.
Thus,
slows
progression
fibrillation
lysozyme.
The Journal of Physical Chemistry B,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 5, 2024
Misfolding
and
amyloid
fibrillogenesis
of
proteins
have
close
relationships
with
several
neurodegenerative
diseases.
The
present
work
investigates
the
inhibitive
activities
ankaflavin
(AK)
monascin
(MS),
two
yellow
pigments
separated
from
Journal of Biomolecular Structure and Dynamics,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 13
Published: Nov. 25, 2024
The
prolific
role
of
bioactive
ligands
in
interacting
with
a
variety
proteins
has
become
focal
point
interest
pharmacokinetics
and
pharmacodynamics,
thus
sparking
substantial
enthusiasm
within
the
realm
medicinal
chemistry.
reversible
binding
small
molecules
is
characteristic
feature,
it's
essential
to
investigate
these
interactions
understand
their
mode
mechanism
action
human
body.
Therefore,
primary
objective
present
study
underlying
by
which
yohimbine
(Yoh)
interacts
protein
myoglobin
(Mb),
employing
both