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Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications

[Image: see text] Protein prenylation is a ubiquitous covalent post-translational modification found in all eukaryotic cells, comprising attachment of either a farnesyl or a geranylgeranyl isoprenoid. It is essential for the proper cellular activity of numerous proteins, including Ras family GTPases...

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Autores principales: Palsuledesai, Charuta C., Distefano, Mark D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301080/
https://www.ncbi.nlm.nih.gov/pubmed/25402849
http://dx.doi.org/10.1021/cb500791f
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author Palsuledesai, Charuta C.
Distefano, Mark D.
author_facet Palsuledesai, Charuta C.
Distefano, Mark D.
author_sort Palsuledesai, Charuta C.
collection PubMed
description [Image: see text] Protein prenylation is a ubiquitous covalent post-translational modification found in all eukaryotic cells, comprising attachment of either a farnesyl or a geranylgeranyl isoprenoid. It is essential for the proper cellular activity of numerous proteins, including Ras family GTPases and heterotrimeric G-proteins. Inhibition of prenylation has been extensively investigated to suppress the activity of oncogenic Ras proteins to achieve antitumor activity. Here, we review the biochemistry of the prenyltransferase enzymes and numerous isoprenoid analogs synthesized to investigate various aspects of prenylation and prenyltransferases. We also give an account of the current status of prenyltransferase inhibitors as potential therapeutics against several diseases including cancers, progeria, aging, parasitic diseases, and bacterial and viral infections. Finally, we discuss recent progress in utilizing protein prenylation for site-specific protein labeling for various biotechnology applications.
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spelling pubmed-43010802015-11-17 Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications Palsuledesai, Charuta C. Distefano, Mark D. ACS Chem Biol [Image: see text] Protein prenylation is a ubiquitous covalent post-translational modification found in all eukaryotic cells, comprising attachment of either a farnesyl or a geranylgeranyl isoprenoid. It is essential for the proper cellular activity of numerous proteins, including Ras family GTPases and heterotrimeric G-proteins. Inhibition of prenylation has been extensively investigated to suppress the activity of oncogenic Ras proteins to achieve antitumor activity. Here, we review the biochemistry of the prenyltransferase enzymes and numerous isoprenoid analogs synthesized to investigate various aspects of prenylation and prenyltransferases. We also give an account of the current status of prenyltransferase inhibitors as potential therapeutics against several diseases including cancers, progeria, aging, parasitic diseases, and bacterial and viral infections. Finally, we discuss recent progress in utilizing protein prenylation for site-specific protein labeling for various biotechnology applications. American Chemical Society 2014-11-17 2015-01-16 /pmc/articles/PMC4301080/ /pubmed/25402849 http://dx.doi.org/10.1021/cb500791f Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Palsuledesai, Charuta C.
Distefano, Mark D.
Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
title Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
title_full Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
title_fullStr Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
title_full_unstemmed Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
title_short Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
title_sort protein prenylation: enzymes, therapeutics, and biotechnology applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301080/
https://www.ncbi.nlm.nih.gov/pubmed/25402849
http://dx.doi.org/10.1021/cb500791f
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