Site-selective protein-modification chemistry for basic biology and drug development

A wide range of different aqueous chemistries for the site-selective modification of proteins have been described over the past decade. This Perspective discusses the scope and potential of chemical site-selective protein-modification methods in the context of their biological and therapeutic applic...

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Veröffentlicht in:Nature chemistry 2016-02, Vol.8 (2), p.103-113
Hauptverfasser: Krall, Nikolaus, da Cruz, Filipa P., Boutureira, Omar, Bernardes, Gonçalo J. L.
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Sprache:eng
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Zusammenfassung:A wide range of different aqueous chemistries for the site-selective modification of proteins have been described over the past decade. This Perspective discusses the scope and potential of chemical site-selective protein-modification methods in the context of their biological and therapeutic applications. Nature has produced intricate machinery to covalently diversify the structure of proteins after their synthesis in the ribosome. In an attempt to mimic nature, chemists have developed a large set of reactions that enable post-expression modification of proteins at pre-determined sites. These reactions are now used to selectively install particular modifications on proteins for many biological and therapeutic applications. For example, they provide an opportunity to install post-translational modifications on proteins to determine their exact biological roles. Labelling of proteins in live cells with fluorescent dyes allows protein uptake and intracellular trafficking to be tracked and also enables physiological parameters to be measured optically. Through the conjugation of potent cytotoxicants to antibodies, novel anti-cancer drugs with improved efficacy and reduced side effects may be obtained. In this Perspective, we highlight the most exciting current and future applications of chemical site-selective protein modification and consider which hurdles still need to be overcome for more widespread use.
ISSN:1755-4330
1755-4349
DOI:10.1038/nchem.2393