Ultrafast Au(III)-Mediated Arylation of Cysteine
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(18), С. 12365 - 12374
Опубликована: Апрель 24, 2024
Through
mechanistic
work
and
rational
design,
we
have
developed
the
fastest
organometallic
abiotic
Cys
bioconjugation.
As
a
result,
Au(III)
bioconjugation
reagents
enable
selective
labeling
of
moieties
down
to
picomolar
concentrations
allow
for
rapid
construction
complex
heterostructures
from
peptides,
proteins,
oligonucleotides.
This
showcases
how
chemistry
can
be
interfaced
with
biomolecules
lead
range
reactivities
that
are
largely
unmatched
by
classical
organic
tools.
Язык: Английский
Organometallic Oxidative Addition Complexes for S-Arylation of Free Cysteines
Bioconjugate Chemistry,
Год журнала:
2024,
Номер
35(7), С. 883 - 889
Опубликована: Июнь 24, 2024
Development
of
bioconjugation
strategies
to
efficiently
modify
biomolecules
is
key
importance
for
fundamental
and
translational
scientific
studies.
Cysteine
Язык: Английский
Harnessing the hydrolytic stability of poly(2-oxazine) living chain-ends for direct aqueous bioconjugations
European Polymer Journal,
Год журнала:
2025,
Номер
unknown, С. 113842 - 113842
Опубликована: Фев. 1, 2025
Язык: Английский
Post-synthetic Chemical Functionalization of Peptides
Elsevier eBooks,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
Язык: Английский
Study of uricase-polynorbornene conjugates derived from grafting-from ring-opening metathesis polymerization
Journal of Materials Chemistry B,
Год журнала:
2024,
Номер
12(8), С. 2197 - 2206
Опубликована: Янв. 1, 2024
Grafting-from
ROMP-derived
polynorbornene-based
UO
conjugates
retain
bioactivity,
improves
stability,
and
evades
anti-PEG
recognition
could
be
a
potential
PEG
alternative.
Язык: Английский
Facile Access to Branched Multispecific Proteins
Bioconjugate Chemistry,
Год журнала:
2024,
Номер
35(7), С. 954 - 962
Опубликована: Июнь 16, 2024
Approaches
that
leverage
orthogonal
chemical
reactions
to
generate
protein–protein
conjugates
have
expanded
access
bespoke
chimeras.
Although
the
literature
is
replete
with
examples
of
semisynthesis
bispecific
proteins,
few
methods
exist
for
protein
higher
complexity
(i.e.,
greater
than
two-protein
fusions).
The
recent
emergence
trispecific
cell
engagers
immune
redirection
therapies
necessitates
development
construction
proteins
would
otherwise
be
inaccessible
via
natural
synthesis.
Here,
we
demonstrate
3-bromo-5-methylene
pyrrolone
(3Br-5MP)
can
used
effect
facile
synthesis
peptides
and
exquisite
control
over
addition
each
monomer.
multimeric
complexes
maintain
epitope
functionality
both
in
human
cells
upon
immobilization.
We
anticipate
using
this
3Br-5MP
will
broad
utility
basic
science
research
quicken
pace
establish
novel,
therapies.
Язык: Английский