Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 24, 2025
Glycans
are
intrinsically
flexible
molecules
that
can
adopt
many
conformations.
These
often
carry
ionic
functional
groups
influence
glycan's
conformational
preferences,
dynamics,
and
aggregation
tendencies.
Inspired
by
these
mechanisms,
we
have
engineered
a
glycan
sequence
whose
secondary
structure
be
precisely
manipulated
using
groups.
We
strategically
incorporated
substituents
into
adopting
hairpin
conformation.
Complementary
stabilized
the
closed
conformers,
while
repulsions
shifted
populations
toward
open
forms.
External
stimuli,
such
as
pH
variations
or
enzyme
addition,
enabled
us
to
dynamically
control
hairpin's
opening
closing.
Additionally,
changes
in
protonation
states
led
aggregation,
suggesting
opportunities
for
creation
of
responsive
glycan-based
materials.
Chemical Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Continuous
porous
aromatic
framework
membranes
were
designed
and
constructed
to
achieve
the
first
example
of
ion
conductive
frameworks
continuous
that
dynamically
respond
chemical
acid/base
stimulus.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
The
chirality
of
helical
polypeptides
is
correlated
to
that
their
constituent
amino
acid
residues.
For
with
non-natural
backbones,
however,
such
correlations
are
less
clear.
Here,
circular
double
helices
torus
knot/link
topologies
were
assembled
from
metal-peptide
chains
composed
Ag(I)
ions
and
ditopic
tripeptides
Gly-Gly-Ala
Gly-Ala-Gly
sequences.
We
found
the
structures
determined
by
l-Ala's
dihedral
angles.
A
tubular
dimeric
structure
an
M21L14
composition
was
further
achieved
via
additional
metal
cross-linking,
showing
rational
design
potential
for
artificial
peptide
helices.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 24, 2025
Glycans
are
intrinsically
flexible
molecules
that
can
adopt
many
conformations.
These
often
carry
ionic
functional
groups
influence
glycan's
conformational
preferences,
dynamics,
and
aggregation
tendencies.
Inspired
by
these
mechanisms,
we
have
engineered
a
glycan
sequence
whose
secondary
structure
be
precisely
manipulated
using
groups.
We
strategically
incorporated
substituents
into
adopting
hairpin
conformation.
Complementary
stabilized
the
closed
conformers,
while
repulsions
shifted
populations
toward
open
forms.
External
stimuli,
such
as
pH
variations
or
enzyme
addition,
enabled
us
to
dynamically
control
hairpin's
opening
closing.
Additionally,
changes
in
protonation
states
led
aggregation,
suggesting
opportunities
for
creation
of
responsive
glycan-based
materials.