Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 23, 2025
Introduction
T-cell
receptors
(TCRs)
play
a
critical
role
in
the
immune
response
by
recognizing
specific
ligand
peptides
presented
major
histocompatibility
complex
(MHC)
molecules.
Accurate
prediction
of
peptide
binding
to
TCRs
is
essential
for
advancing
immunotherapy,
vaccine
design,
and
understanding
mechanisms
autoimmune
disorders.
Methods
This
study
presents
theoretical
approach
that
explores
impact
feature
selection
techniques
on
enhancing
predictive
accuracy
models
tailored
TCRs.
To
evaluate
our
across
different
TCR
systems,
we
utilized
dataset
includes
libraries
tested
against
three
distinct
murine
A
broad
range
physicochemical
properties,
including
amino
acid
composition,
dipeptide
tripeptide
features,
were
integrated
into
machine
learning-based
framework
identify
key
properties
contributing
affinity.
Results
Our
analysis
reveals
leveraging
optimized
subsets
not
only
simplifies
model
complexity
but
also
enhances
performance,
enabling
more
precise
identification
interactions.
The
results
method
are
consistent
with
findings
from
hybrid
approaches
utilize
both
sequence
structural
data
as
input
well
experimental
data.
Discussion
highlights
peptide-TCR
interactions,
providing
quantitative
tool
uncovering
molecular
assisting
design
advanced
targeted
therapeutics.
Nucleic Acids Research,
Journal Year:
2023,
Volume and Issue:
51(W1), P. W569 - W576
Published: May 4, 2023
Abstract
The
cellular
immune
system,
which
is
a
critical
component
of
human
immunity,
uses
T
cell
receptors
(TCRs)
to
recognize
antigenic
proteins
in
the
form
peptides
presented
by
major
histocompatibility
complex
(MHC)
proteins.
Accurate
definition
structural
basis
TCRs
and
their
engagement
peptide–MHCs
can
provide
insights
into
normal
aberrant
help
guide
design
vaccines
immunotherapeutics.
Given
limited
amount
experimentally
determined
TCR–peptide–MHC
structures
vast
within
each
individual
as
well
targets,
accurate
computational
modeling
approaches
are
needed.
Here,
we
report
update
our
web
server,
TCRmodel,
was
originally
developed
model
unbound
from
sequence,
now
complexes
utilizing
several
adaptations
AlphaFold.
This
method,
named
TCRmodel2,
allows
users
submit
sequences
through
an
easy-to-use
interface
shows
similar
or
greater
accuracy
than
AlphaFold
other
methods
based
on
benchmarking.
It
generate
models
15
minutes,
output
provided
with
confidence
scores
integrated
molecular
viewer.
TCRmodel2
available
at
https://tcrmodel.ibbr.umd.edu.
npj Vaccines,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Jan. 20, 2024
Computer-aided
discovery
of
vaccine
targets
has
become
a
cornerstone
rational
design.
In
this
article,
I
discuss
how
Machine
Learning
(ML)
can
inform
and
guide
key
computational
steps
in
design
concerned
with
the
identification
B
T
cell
epitopes
correlates
protection.
provide
examples
ML
models,
as
well
types
data
predictions
for
which
they
are
built.
argue
that
interpretable
potential
to
improve
immunogens
also
tool
scientific
discovery,
by
helping
elucidate
molecular
processes
underlying
vaccine-induced
immune
responses.
outline
limitations
challenges
terms
availability
method
development
need
be
addressed
bridge
gap
between
advances
their
translational
application
Proceedings of the National Academy of Sciences,
Journal Year:
2024,
Volume and Issue:
121(24)
Published: June 5, 2024
The
accurate
prediction
of
binding
between
T
cell
receptors
(TCR)
and
their
cognate
epitopes
is
key
to
understanding
the
adaptive
immune
response
developing
immunotherapies.
Current
methods
face
two
significant
limitations:
shortage
comprehensive
high-quality
data
bias
introduced
by
selection
negative
training
commonly
used
in
supervised
learning
approaches.
We
propose
a
method,
Transformer-based
Unsupervised
Language
model
for
Interacting
Peptides
(TULIP),
that
addresses
both
limitations
leveraging
incomplete
unsupervised
using
transformer
architecture
language
models.
Our
flexible
integrates
all
possible
sources,
regardless
quality
or
completeness.
demonstrate
existence
sampling
procedure
previous
approaches,
emphasizing
need
an
approach.
TULIP
recognizes
specific
TCRs
epitope,
performing
well
on
unseen
epitopes.
outperforms
state-of-the-art
models
offers
promising
direction
development
more
TCR
epitope
recognition
Journal of Chemical Theory and Computation,
Journal Year:
2023,
Volume and Issue:
19(16), P. 5315 - 5333
Published: Aug. 1, 2023
The
design
of
new
biomolecules
able
to
harness
immune
mechanisms
for
the
treatment
diseases
is
a
prime
challenge
computational
and
simulative
approaches.
For
instance,
in
recent
years,
antibodies
have
emerged
as
an
important
class
therapeutics
against
spectrum
pathologies.
In
cancer,
immune-inspired
approaches
are
witnessing
surge
thanks
better
understanding
tumor-associated
antigens
their
engagement
or
evasion
from
human
system.
Here,
we
provide
summary
main
state-of-the-art
that
used
antigens,
parallel,
review
key
methodologies
epitope
identification
both
B-
T-cell
mediated
responses.
A
special
focus
devoted
description
structure-
physics-based
models,
privileged
over
purely
sequence-based
We
discuss
implications
novel
methods
engineering
with
tailored
immunological
properties
possible
therapeutic
uses.
Finally,
highlight
extraordinary
challenges
opportunities
presented
by
integration
emerging
Artificial
Intelligence
technologies
prediction
epitopes,
antibodies.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(20)
Published: May 15, 2024
Reliable
prediction
of
T
cell
specificity
against
antigenic
signatures
is
a
formidable
task,
complicated
by
the
immense
diversity
receptor
and
antigen
sequence
space
resulting
limited
availability
training
sets
for
inferential
models.
Recent
modeling
efforts
have
demonstrated
advantage
incorporating
structural
information
to
overcome
need
extensive
data,
yet
disentangling
heterogeneous
TCR-antigen
interface
accurately
predict
MHC-allele-restricted
TCR-peptide
interactions
has
remained
challenging.
Here,
we
present
RACER-m,
coarse-grained
model
leveraging
key
biophysical
from
publicly
available
crystal
structures.
Explicit
inclusion
content
substantially
reduces
required
number
examples
maintains
reliable
predictions
TCR-recognition
sensitivity
across
diverse
biological
contexts.
Our
capably
identifies
biophysically
meaningful
point-mutant
peptides
that
affect
binding
affinity,
distinguishing
its
ability
in
predicting
TCR
point-mutants
alternative
sequence-based
methods.
Its
application
broadly
applicable
studies
involving
both
closely
related
structurally
pairs.