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Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes
Posttranslational attachment of lipids to proteins is important for many cellular functions, and the enzymes responsible for these modifications are implicated in many diseases, from cancer to neurodegeneration. Lipid transferases and hydrolases are increasingly tractable therapeutic targets, but pr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855259/ https://www.ncbi.nlm.nih.gov/pubmed/31762980 http://dx.doi.org/10.1039/c9sc01785b |
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author | Lanyon-Hogg, Thomas Ritzefeld, Markus Sefer, Lea Bickel, Jasmine K. Rudolf, Amalie F. Panyain, Nattawadee Bineva-Todd, Ganka Ocasio, Cory A. O'Reilly, Nicola Siebold, Christian Magee, Anthony I. Tate, Edward W. |
author_facet | Lanyon-Hogg, Thomas Ritzefeld, Markus Sefer, Lea Bickel, Jasmine K. Rudolf, Amalie F. Panyain, Nattawadee Bineva-Todd, Ganka Ocasio, Cory A. O'Reilly, Nicola Siebold, Christian Magee, Anthony I. Tate, Edward W. |
author_sort | Lanyon-Hogg, Thomas |
collection | PubMed |
description | Posttranslational attachment of lipids to proteins is important for many cellular functions, and the enzymes responsible for these modifications are implicated in many diseases, from cancer to neurodegeneration. Lipid transferases and hydrolases are increasingly tractable therapeutic targets, but present unique challenges for high-throughput biochemical enzyme assays which hinder development of new inhibitors. We present Acylation-coupled Lipophilic Induction of Polarisation (Acyl-cLIP) as the first universally applicable biochemical lipidation assay, exploiting the hydrophobic nature of lipidated peptides to drive a polarised fluorescence readout. Acyl-cLIP allows sensitive, accurate, real-time measurement of S- or N-palmitoylation, N-myristoylation, S-farnesylation or S-geranylgeranylation. Furthermore, it is applicable to transfer and hydrolysis reactions, and we demonstrate its extension to a high-throughput screening format. We anticipate that Acyl-cLIP will greatly expedite future drug discovery efforts against these challenging targets. |
format | Online Article Text |
id | pubmed-6855259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-68552592019-11-22 Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes Lanyon-Hogg, Thomas Ritzefeld, Markus Sefer, Lea Bickel, Jasmine K. Rudolf, Amalie F. Panyain, Nattawadee Bineva-Todd, Ganka Ocasio, Cory A. O'Reilly, Nicola Siebold, Christian Magee, Anthony I. Tate, Edward W. Chem Sci Chemistry Posttranslational attachment of lipids to proteins is important for many cellular functions, and the enzymes responsible for these modifications are implicated in many diseases, from cancer to neurodegeneration. Lipid transferases and hydrolases are increasingly tractable therapeutic targets, but present unique challenges for high-throughput biochemical enzyme assays which hinder development of new inhibitors. We present Acylation-coupled Lipophilic Induction of Polarisation (Acyl-cLIP) as the first universally applicable biochemical lipidation assay, exploiting the hydrophobic nature of lipidated peptides to drive a polarised fluorescence readout. Acyl-cLIP allows sensitive, accurate, real-time measurement of S- or N-palmitoylation, N-myristoylation, S-farnesylation or S-geranylgeranylation. Furthermore, it is applicable to transfer and hydrolysis reactions, and we demonstrate its extension to a high-throughput screening format. We anticipate that Acyl-cLIP will greatly expedite future drug discovery efforts against these challenging targets. Royal Society of Chemistry 2019-07-01 /pmc/articles/PMC6855259/ /pubmed/31762980 http://dx.doi.org/10.1039/c9sc01785b Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Lanyon-Hogg, Thomas Ritzefeld, Markus Sefer, Lea Bickel, Jasmine K. Rudolf, Amalie F. Panyain, Nattawadee Bineva-Todd, Ganka Ocasio, Cory A. O'Reilly, Nicola Siebold, Christian Magee, Anthony I. Tate, Edward W. Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes |
title | Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes
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title_full | Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes
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title_fullStr | Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes
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title_full_unstemmed | Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes
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title_short | Acylation-coupled lipophilic induction of polarisation (Acyl-cLIP): a universal assay for lipid transferase and hydrolase enzymes
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title_sort | acylation-coupled lipophilic induction of polarisation (acyl-clip): a universal assay for lipid transferase and hydrolase enzymes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855259/ https://www.ncbi.nlm.nih.gov/pubmed/31762980 http://dx.doi.org/10.1039/c9sc01785b |
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