Using an azobenzene cross-linker to either increase or decrease peptide helix content upon trans-to-cis photoisomerization.
about
Light-activated ion channels for remote control of neuronal firingSpectroscopic studies of protein folding: linear and nonlinear methodsFolding and unfolding of a photoswitchable peptide from picoseconds to microseconds.Controlling the enzymatic activity of a restriction enzyme by light.Alpha-helix formation in a photoswitchable peptide tracked from picoseconds to microseconds by time-resolved IR spectroscopy.Synthesis of cell-permeable stapled BH3 peptide-based Mcl-1 inhibitors containing simple aryl and vinylaryl cross-linkers.Mechanisms of photoswitch conjugation and light activation of an ionotropic glutamate receptor.Bis-azobenzene crosslinkers for photocontrol of peptide structure.Azobenzene photoswitches for biomolecules.An enhanced functional interrogation/manipulation of intracellular signaling pathways with the peptide 'stapling' technology.Constrained peptides as miniature protein structuresReview stapling peptides using cysteine crosslinking.Facile synthesis of stapled, structurally reinforced peptide helices via a photoinduced intramolecular 1,3-dipolar cycloaddition reaction.Optimizing the Photocontrol of bZIP Coiled Coils with Azobenzene Crosslinkers: Role of the Crosslinking Site.Chiral tether-mediated stabilization and helix-sense control of complementary metallo-double helices.A stable miniature protein with oxaloacetate decarboxylase activity.The effect of azobenzene cross-linker position on the degree of helical peptide photo-control.Bidirectional photocontrol of peptide conformation with a bridged azobenzene derivative.Remote control over folding by light.Azobenzene photocontrol of peptides and proteins.A biomimetic molecular switch at work: coupling photoisomerization dynamics to peptide structural rearrangement.Synthesis of directly linked diazine isosteres of pyrrole-polyamide that photochemically cleave DNA.Selective photoregulation of the activity of glycogen synthase and glycogen phosphorylase, two key enzymes in glycogen metabolism.
P2860
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P2860
Using an azobenzene cross-linker to either increase or decrease peptide helix content upon trans-to-cis photoisomerization.
description
2002 nî lūn-bûn
@nan
2002 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մարտին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Using an azobenzene cross-link ...... ans-to-cis photoisomerization.
@ast
Using an azobenzene cross-link ...... ans-to-cis photoisomerization.
@en
type
label
Using an azobenzene cross-link ...... ans-to-cis photoisomerization.
@ast
Using an azobenzene cross-link ...... ans-to-cis photoisomerization.
@en
prefLabel
Using an azobenzene cross-link ...... ans-to-cis photoisomerization.
@ast
Using an azobenzene cross-link ...... ans-to-cis photoisomerization.
@en
P1476
Using an azobenzene cross-link ...... rans-to-cis photoisomerization
@en
P2093
Daniel G Flint
Janet R Kumita
P304
P356
10.1016/S1074-5521(02)00109-6
P577
2002-03-01T00:00:00Z