About: Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation

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About: Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation Goto Sponge NotDistinct Permalink

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scientific article published on 07 July 2011

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2011 (uk) article scientifique publié en 2011 (fr) im August 2011 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 07 July 2011 (en) artículu científicu espublizáu en xunetu de 2011 (ast)
publication date	wds:Q59319678-87BD6F49-0BB6-437F-A3AE-29F7B4FAABC1
publication date	2011-07-07 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59319678-3129804F-00D0-4C31-ACDD-B4E995D217E7
language of work or name	English
cites work	wds:Q59319678-795D9BEC-6013-4916-B083-909B78989373
cites work	A Comparative Study of Bioorthogonal Reactions with Azides
author name string	wds:Q59319678-228262A8-B949-43DE-A593-F3798BF45428 wds:Q59319678-61D22959-44A5-4A0D-B91B-9C731D97DA53 wds:Q59319678-6FDFB134-DC7A-4B38-9E71-C6B76A7F78EF wds:Q59319678-7304E1E0-D6FA-4C28-B4EF-516F80A68B7F wds:Q59319678-C26C6CA3-EC1A-4AE7-AA69-9015841F325F
author name string	Matthew Holt Tom W Muir Jason W Chin Thomas Elliott Duy P Nguyen
rdfs:label	Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation (en) Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation (nl)
skos:prefLabel	Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation (en) Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation (nl)
name	Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation (en) Genetically Encoded 1,2-Aminothiols Facilitate Rapid and Site-Specific Protein Labeling via a Bio-orthogonal Cyanobenzothiazole Condensation (nl)
title	wds:Q59319678-9E9EB48F-2C8D-4A9A-9949-6325E121982C
title	Genetically encoded 1,2-aminothiols facilitate rapid and site-specific protein labeling via a bio-orthogonal cyanobenzothiazole condensation (en)
page(s)	wds:Q59319678-16D65B23-A3D3-41BB-AB8F-63B2E15B4E58
page(s)	11418-11421
instance of	wds:Q59319678-258E6E21-0162-4085-B698-C2DE24A26510
instance of	scholarly article
PubMed ID	wds:Q59319678-075F4DA3-DDDC-4716-A8A7-7824C9FA8912
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21736333
PubMed ID	21736333
published in	wds:Q59319678-F8E27DE8-1574-450F-B66B-082EA20A4C62
published in	Journal of the American Chemical Society
issue	wds:Q59319678-67227E44-BDD6-49BA-BE64-F33D486ED2CE
volume	wds:Q59319678-B9F2EF76-F233-49A9-BAEF-BB9628928BAB
issue	30
volume	133
DOI	wds:Q59319678-6F7B57EB-2C5C-40B2-B902-68302D2B9ACC
DOI	http://dx.doi.org/10.1021/JA203111C
DOI	10.1021/JA203111C
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59319678
is cites work of	Genetic Encoding of bicyclononynes and trans-cyclooctenes for site-specific protein labeling in vitro and in live mammalian cells via rapid fluorogenic Diels-Alder reactions Ribosomal Synthesis of Macrocyclic Peptides in Vitro and in Vivo Mediated by Genetically Encoded Aminothiol Unnatural Amino Acids Transition metal-mediated bioorthogonal protein chemistry in living cells. Designer proteins: applications of genetic code expansion in cell biology Expanding the genetic code of an animal Designing logical codon reassignment - Expanding the chemistry in biology Strategy for dual-analyte luciferin imaging: in vivo bioluminescence detection of hydrogen peroxide and caspase activity in a murine model of acute inflammation A biocompatible in vivo ligation reaction and its application for noninvasive bioluminescent imaging of protease activity in living mice. Site-specific antibody-drug conjugates: the nexus of bioorthogonal chemistry, protein engineering, and drug development Selective RNA versus DNA G-quadruplex targeting by in situ click chemistry. Labeling proteins with fluorophore/thioamide Förster resonant energy transfer pairs by combining unnatural amino acid mutagenesis and native chemical ligation A genetically encoded acrylamide functionality Genetically encoded norbornene directs site-specific cellular protein labelling via a rapid bioorthogonal reaction Protein conjugation with genetically encoded unnatural amino acids Application of the protein semisynthesis strategy to the generation of modified chromatin Sequence-Specific 2-Cyanobenzothiazole Ligation Strain-promoted sydnone bicyclo-[6.1.0]-nonyne cycloaddition†Electronic supplementary information (ESI) available: Full experimental details, (1)H/(13)C NMR spectral data, protein synthesis and purification. See DOI: 10.1039/c3sc53332h Genetically encoded tetrazine amino acid directs rapid site-specific in vivo bioorthogonal ligation with trans-cyclooctenes Pyrrolysyl-tRNA synthetase: an ordinary enzyme but an outstanding genetic code expansion tool An asymmetric synthesis of L-pyrrolysine Specific and quantitative labeling of biomolecules using click chemistry Concerted, rapid, quantitative, and site-specific dual labeling of proteins Comparison of strategies for non-perturbing labeling of α-synuclein to study amyloidogenesis Cell-free co-production of an orthogonal transfer RNA activates efficient site-specific non-natural amino acid incorporation. Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation. A novel approach to the site-selective dual labelling of a protein via chemoselective cysteine modification. Targeting the N terminus for site-selective protein modification Site-specific protection and dual labeling of human epidermal growth factor (hEGF) for targeting, imaging, and cargo delivery. Economical and scalable synthesis of 6-amino-2-cyanobenzothiazole A simple bioluminescent method for measuring D-amino acid oxidase activity Cysteine-Mediated Intracellular Building of Luciferin to Enhance Probe Retention and Fluorescence Turn-On. Proline editing: a general and practical approach to the synthesis of functionally and structurally diverse peptides. Analysis of steric versus stereoelectronic effects of 4-substituted prolines on conformation within peptides Chemical Methodology for Labelling and Bioconjugation Visualizing biologically active small molecules in cells using click chemistry Fast and selective labeling of N-terminal cysteines at neutral pH via thiazolidino boronate formation. Multiple site-selective insertions of noncanonical amino acids into sequence-repetitive polypeptides. Rapid and specific post-synthesis modification of DNA through a biocompatible condensation of 1,2-aminothiols with 2-cyanobenzothiazole. Bioconjugation of therapeutic proteins and enzymes using the expanded set of genetically encoded amino acids Site-specific immobilization of biomolecules by a biocompatible reaction between terminal cysteine and 2-cyanobenzothiazole. Experimental challenges of sense codon reassignment: an innovative approach to genetic code expansion Genetically encoded libraries of nonstandard peptides A molecular engineering toolbox for the structural biologist. Recent developments of genetically encoded optical sensors for cell biology Pyrrolysine Amber Stop-Codon Suppression: Development and Applications. Genetic incorporation of 1,2-aminothiol functionality for site-specific protein modification via thiazolidine formation. A need for speed: genetic encoding of rapid cycloaddition chemistries for protein labelling in living cells. Multiply labeling proteins for studies of folding and stability Orthogonal Protein Translation Using Pyrrolysyl-tRNA Synthetases for Single- and Multiple-Noncanonical Amino Acid Mutagenesis. Computation-Guided Rational Design of a Peptide Motif That Reacts with Cyanobenzothiazoles via Internal Cysteine-Lysine Relay Chemically-defined lactose-based autoinduction medium for site-specific incorporation of non-canonical amino acids into proteins. Micelle-Enhanced Bioorthogonal Labeling of Genetically Encoded Azido Groups on the Lipid-Embedded Surface of a GPCR. A biocompatible "split luciferin" reaction and its application for non-invasive bioluminescent imaging of protease activity in living animals

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