About: Functionalised staple linkages for modulating the cellular activity of stapled peptides

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована у 2014 (uk) im Januar 2014 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57540612-2D70F967-91AC-414C-B770-49C0848A73AF
publication date	2014-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q57540612-C144020D-DF24-4454-BF24-064C85AF43AB
cites work	Bioorthogonal chemistry: fishing for selectivity in a sea of functionality
author name string	wds:Q57540612-0CA22D53-977A-45AC-8C12-AAE961099F7E wds:Q57540612-14153741-1621-491D-9776-B62B95D20853 wds:Q57540612-14337EBB-D898-4D65-806B-9EB59F1724A4 wds:Q57540612-238FC7B3-60E1-4D79-9841-23BAEBDD01E3 wds:Q57540612-2A596D42-2137-48CE-BD93-C06DD96A69F1 wds:Q57540612-401D6D2D-6DC7-47D7-953B-8CE89FC8087E wds:Q57540612-630E0803-976C-4580-AB5A-506028B87AB5 wds:Q57540612-78FE796C-F8E9-49A5-9219-D983EC1C2D1D wds:Q57540612-816B86AA-43F7-436D-881E-D00A50AD33BE wds:Q57540612-A3361BBB-57FB-49A0-906B-3E0064B4551F wds:Q57540612-B90B6F05-7F98-4981-9C76-8562926F92E6 wds:Q57540612-CA773F8B-F826-4203-A86E-08B2081DEFC7 wds:Q57540612-CC47211E-0523-48F0-A53B-D5B81E7D77B6 wds:Q57540612-FC7EE1E2-0537-4E3F-AA20-676FEE94122D
author name string	Marko Hyvönen Chandra Verma Peterson de Andrade Luca Laraia David R. Spring Christopher J. Brown Niklas Sköld Tze Jing Sum David P. Lane Ashok R. Venkitaraman Laura S. Itzhaki Pamela J. E. Rowling Soo-Tng Quah Thomas L. Joseph
rdfs:label	Functionalised staple linkages for modulating the cellular activity of stapled peptides (en) Functionalised staple linkages for modulating the cellular activity of stapled peptides (nl)
skos:prefLabel	Functionalised staple linkages for modulating the cellular activity of stapled peptides (en) Functionalised staple linkages for modulating the cellular activity of stapled peptides (nl)
name	Functionalised staple linkages for modulating the cellular activity of stapled peptides (en) Functionalised staple linkages for modulating the cellular activity of stapled peptides (nl)
author	wds:Q57540612-4859537C-48DD-4C2D-8DD8-F5EB2E7E3FEF wds:Q57540612-EE8AE353-3EE5-4184-BDA4-9179ECE25C26
author	Yu Heng Lau Maxim Rossmann
title	wds:Q57540612-3876439D-A6EE-490B-A9F7-5495C0A82F4E
title	Functionalised staple linkages for modulating the cellular activity of stapled peptides (en)
page(s)	wds:Q57540612-B08E628B-D2AD-4FCA-B18D-EAC761A124B6
page(s)	1804-1809
instance of	wds:Q57540612-CE25A776-6EF1-4D9E-A17F-5ACA355BDC20
instance of	scholarly article
published in	wds:Q57540612-C0804342-57DA-4DDD-AD8E-8B4D5434AA22
published in	Chemical Science
issue	wds:Q57540612-6514E049-384B-4BE3-B762-1F97D1679195
volume	wds:Q57540612-6400D649-192B-4D1F-BC86-175134062C85
issue	5
volume	5
DOI	wds:Q57540612-F1A595C5-1733-40B4-BC68-AC86A4791B07
DOI	http://dx.doi.org/10.1039/C4SC00045E
DOI	10.1039/C4SC00045E
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57540612
is cites work of	Double Strain-Promoted Macrocyclization for the Rapid Selection of Cell-Active Stapled Peptides Investigating peptide sequence variations for 'double-click' stapled p53 peptides A two-component 'double-click' approach to peptide stapling. Structure-Based Design of Inhibitors of Protein-Protein Interactions: Mimicking Peptide Binding Epitopes. Linear aliphatic dialkynes as alternative linkers for double-click stapling of p53-derived peptides An In-tether Chiral Center Modulates the Helicity, Cell Permeability, and Target Binding Affinity of a Peptide. A New Methodology for Incorporating Chiral Linkers into Stapled Peptides Development of a Multifunctional Benzophenone Linker for Peptide Stapling and Photoaffinity Labelling Modulating protein-protein interactions: the potential of peptides Acetone-Linked Peptides: A Convergent Approach for Peptide Macrocyclization and Labeling Oxidative diversification of amino acids and peptides by small-molecule iron catalysis Development of cell-penetrating peptide-based drug leads to inhibit MDMX:p53 and MDM2:p53 interactions. An in-tether chiral center modulates the proapoptotic activity of the KLA peptide. Stapling of unprotected helical peptides via photo-induced intramolecular thiol-yne hydrothiolation. Application of Thiol-yne/Thiol-ene Reactions for Peptide and Protein Macrocyclizations. Phage-displayed macrocyclic glycopeptide libraries Crosslinked Aspartic Acids as Helix-Nucleating Templates. Hydrocarbon constrained peptides - understanding preorganisation and binding affinity Double quick, double click reversible peptide "stapling". Divergent unprotected peptide macrocyclisation by palladium-mediated cysteine arylation. The future perspectives of natural materials for pulmonary drug delivery and lung tissue engineering Development of Cell-Permeable, Non-Helical Constrained Peptides to Target a Key Protein-Protein Interaction in Ovarian Cancer Development of Cell-Permeable, Non-Helical Constrained Peptides to Target a Key Protein-Protein Interaction in Ovarian Cancer Improving cell penetration of helical peptides stabilized by N-terminal crosslinked aspartic acids. Bridged Analogues for p53-Dependent Cancer Therapy Obtained by S-Alkylation Chiral Sulfoxide-Induced Single Turn Peptide α-Helicity. Stabilization of peptides against proteolysis through disulfide-bridged conjugation with synthetic aromatics. Targeting the Genome-Stability Hub Ctf4 by Stapled-Peptide Design. Diversity-Oriented Peptide Stapling: A Third Generation Copper-Catalysed Azide-Alkyne Cycloaddition Stapling and Functionalisation Strategy. Bioconjugation - using selective chemistry to enhance the properties of proteins and peptides as therapeutics and carriers Effect of Stapling Architecture on Physiochemical Properties and Cell Permeability of Stapled α-Helical Peptides: A Comparative Study. Locking Interconversion of Aromatic Oligoamide Foldamers by Intramolecular Side-chain Crosslinking: toward Absolute Control of Helicity in Synthetic Aromatic Foldamers. An enhanced functional interrogation/manipulation of intracellular signaling pathways with the peptide 'stapling' technology Receptor-templated stapling of intrinsically disordered peptide ligands. Enhanced Permeability and Binding Activity of Isobutylene-Grafted Peptides. A proline-derived transannular N-cap for nucleation of short α-helical peptides. Azide-rich peptides via an on-resin diazotransfer reaction

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