bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 23, 2023
Motivation:
Charged
amino
acid
residues
on
the
spike
protein
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
have
been
shown
to
influence
its
binding
different
cell
surface
receptors,
non-specific
electrostatic
interactions
with
environment,
and
structural
stability
conformation.
It
is
therefore
important
obtain
a
good
understanding
mutations
that
affect
total
charge
which
arisen
across
SARS-CoV-2
lineages
during
course
virus'
evolution.
Results:
We
analyse
change
in
number
ionizable
acids
corresponding
proteins
almost
2200
emerged
over
span
pandemic.
Our
results
show
previously
observed
trend
toward
an
increase
positive
variants
concern
has
essentially
stopped
emergence
early
omicron
variants.
Furthermore,
recently
greater
diversity
terms
their
composition
acids.
also
demonstrate
patterns
are
characteristic
related
within
broader
clade
division
phylogenetic
tree.
Due
ubiquity
biological
our
findings
relevant
for
broad
range
studies
dealing
environment.
Availability:
The
data
underlying
article
available
online
Supplementary
Material.
Journal of Medical Virology,
Journal Year:
2023,
Volume and Issue:
95(10)
Published: Oct. 1, 2023
The
on-going
emergence
of
the
Omicron
BA.2.86
variant
is
one
major
events
in
SARS-CoV-2
genetic
evolution
that
remain
enigmatic
regarding
overall
virus
mutation
rate,
together
with
initial
variant,
BA.1.
Indeed,
genomes
lineage,
an
offspring
second
subvariant,
BA.2,
harbor
39
additional
mutations
spike
compared
to
this
ancestor.
Here
we
comment
on
phylogeny
BA.2.86,
positions,
and
frequencies
other
SARS-CoV-2,
its
spike,
structural
model
protein
concentrates
most
mutations.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(12), P. 1836 - 1836
Published: Nov. 27, 2024
Most
studies
on
the
docking
of
ivermectin
spike
protein
SARS-CoV-2
concern
receptor
binding
domain
(RBD)
and,
more
precisely,
RBD
interface
recognized
by
ACE2
receptor.
The
N-terminal
(NTD),
which
controls
initial
attachment
virus
to
lipid
raft
gangliosides,
has
not
received
attention
it
deserves.
In
this
study,
we
combined
molecular
modeling
and
physicochemical
approaches
analyze
mode
interaction
with
NTD-facing
rafts
host
cell
membrane.
We
characterize
a
area
that
presents
point
mutations
deletions
in
successive
variants
from
strain
omicron
KP.3
circulating
many
countries
2024.
show
exceptional
flexibility,
allowing
drug
bind
all
tested.
energy
is
specific
each
variant,
classification
according
their
affinity
for
following
ascending
order:
Omicron
<
Delta
BA.5
Alpha
Wuhan
(B.1)
BA.1.
site
subject
important
variations
NTD,
including
Y144
deletion.
It
overlaps
ganglioside
as
demonstrated
studies.
These
results
suggest
new
mechanism
antiviral
action
based
competitive
inhibition
rafts.
current
variant
still
ivermectin,
although
an
slightly
lower
than
strain.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 23, 2023
Motivation:
Charged
amino
acid
residues
on
the
spike
protein
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
have
been
shown
to
influence
its
binding
different
cell
surface
receptors,
non-specific
electrostatic
interactions
with
environment,
and
structural
stability
conformation.
It
is
therefore
important
obtain
a
good
understanding
mutations
that
affect
total
charge
which
arisen
across
SARS-CoV-2
lineages
during
course
virus'
evolution.
Results:
We
analyse
change
in
number
ionizable
acids
corresponding
proteins
almost
2200
emerged
over
span
pandemic.
Our
results
show
previously
observed
trend
toward
an
increase
positive
variants
concern
has
essentially
stopped
emergence
early
omicron
variants.
Furthermore,
recently
greater
diversity
terms
their
composition
acids.
also
demonstrate
patterns
are
characteristic
related
within
broader
clade
division
phylogenetic
tree.
Due
ubiquity
biological
our
findings
relevant
for
broad
range
studies
dealing
environment.
Availability:
The
data
underlying
article
available
online
Supplementary
Material.