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Open AccessJournal ArticleDOI

Chemical reporters for biological discovery

Markus Grammel, +1 more
- 01 Aug 2013 - 
- Vol. 9, Iss: 8, pp 475-484
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TLDR
How chemical reporters in conjunction with bioorthogonal labeling methods can be used to image and retrieve nucleic acids, proteins, glycans, lipids and other metabolites in vitro, in cells as well as in whole organisms is reviewed.
Abstract
Functional tools are needed to understand complex biological systems. Here we review how chemical reporters in conjunction with bioorthogonal labeling methods can be used to image and retrieve nucleic acids, proteins, glycans, lipids and other metabolites in vitro, in cells as well as in whole organisms. By tagging these biomolecules, researchers can now monitor their dynamics in living systems and discover specific substrates of cellular pathways. These advances in chemical biology are thus providing important tools to characterize biological pathways and are poised to facilitate our understanding of human diseases.

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Illuminating biological processes through site-specific protein labeling

TL;DR: This tutorial review introduces various strategies for site-specific protein labeling that utilize artificial peptide sequences or genetically encoded UAAs as the labeling handle and introduces the recently emerged dual site- specific protein labeling strategies.
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Illumination of growth, division and secretion by metabolic labeling of the bacterial cell surface

TL;DR: This review describes aspects of bacterial growth, division and secretion that have recently been uncovered by metabolic labeling of the cell envelope and discusses the potential of these techniques for translational applications.
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Global, in situ, site-specific analysis of protein S-sulfenylation

TL;DR: This protocol describes global, in situ, site-specific analysis of protein S-sulfenylation using sulfenic acid–specific chemical probes and mass spectrometry (MS)-based proteomics and outlines strategies for quantitative analysis of this modification in cells responding to redox perturbations.
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Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells

TL;DR: A versatile light-controlled bioorthogonal catalyst built by modifying macroporous silica-Pd0 with supramolecular complex of azobenzene and β-cyclodextrin that can be regulated by light-induced structural changes, mimicking allosteric regulation mechanism of bio-enzymes.
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Optimized Tetrazine Derivatives for Rapid Bioorthogonal Decaging in Living Cells

TL;DR: 3,6-substituted TZ derivatives showed remarkably enhanced decaging rates, enabling rapid iDA-mediated protein activation in living cells and promoted us to design and test unsymmetric TZs bearing an EWG group and a small non-EWG group at the 3- and 6-position.
References
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Journal ArticleDOI

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TL;DR: In this paper, a set of powerful, highly reliable, and selective reactions for the rapid synthesis of useful new compounds and combinatorial libraries through heteroatom links (C-X-C), an approach called click chemistry is defined, enabled, and constrained by a handful of nearly perfect "springloaded" reactions.
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Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine

TL;DR: This study raises the possibility that DNA demethylation may occur through Tet-catalyzed oxidation followed by decarboxylation, and identifies two previously unknown cytosine derivatives in genomic DNA as the products of Tet proteins.
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Tet-Mediated Formation of 5-Carboxylcytosine and Its Excision by TDG in Mammalian DNA

TL;DR: It is demonstrated that 5mC and 5hmC in DNA are oxidized to 5-carboxylcytosine (5caC) by Tet dioxygenases in vitro and in cultured cells, suggesting that oxidation of 5m C by Tet proteins followed by TDG-mediated base excision of 5caC constitutes a pathway for active DNA demethylation.
Journal ArticleDOI

1,3-Dipolar Cycloadditions. Past and Future†

TL;DR: In contrast to the very large number of special methods applicable to syntheses in the heterocyclic series, relatively few general methods are available as discussed by the authors, and the 1,3-dipolar addition offers a remarkably wide range of utility in the synthesis of five-membered heterocycles.
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