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Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities

Recently, peptide microarrays have been used to distinguish proteins, antibodies, viruses, and bacteria based on their binding to random sequence peptides. We reported on the use of peptide arrays to identify enzyme modulators that involve screening an array of 10,000 defined and addressable peptide...

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Detalles Bibliográficos
Autor principal: Fu, Jinglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487955/
https://www.ncbi.nlm.nih.gov/pubmed/28445435
http://dx.doi.org/10.3390/microarrays6020008
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author Fu, Jinglin
author_facet Fu, Jinglin
author_sort Fu, Jinglin
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description Recently, peptide microarrays have been used to distinguish proteins, antibodies, viruses, and bacteria based on their binding to random sequence peptides. We reported on the use of peptide arrays to identify enzyme modulators that involve screening an array of 10,000 defined and addressable peptides on a microarray. Primary peptides were first selected to inhibit the enzyme at low μM concentrations. Then, new peptides were found to only bind strongly with the enzyme–inhibitor complex, but not the native enzyme. These new peptides served as secondary inhibitors that enhanced the inhibition of the enzyme together with the primary peptides. Without the primary peptides, the secondary effect peptides had little effect on the enzyme activity. Conversely, we also selected peptides that recovered the activities of inhibited enzyme–peptide complex. The selection of cooperative peptide pairs will provide a versatile toolkit for modulating enzyme functions, which may potentially be applied to drug discovery and biocatalysis.
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spelling pubmed-54879552017-06-30 Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities Fu, Jinglin Microarrays (Basel) Article Recently, peptide microarrays have been used to distinguish proteins, antibodies, viruses, and bacteria based on their binding to random sequence peptides. We reported on the use of peptide arrays to identify enzyme modulators that involve screening an array of 10,000 defined and addressable peptides on a microarray. Primary peptides were first selected to inhibit the enzyme at low μM concentrations. Then, new peptides were found to only bind strongly with the enzyme–inhibitor complex, but not the native enzyme. These new peptides served as secondary inhibitors that enhanced the inhibition of the enzyme together with the primary peptides. Without the primary peptides, the secondary effect peptides had little effect on the enzyme activity. Conversely, we also selected peptides that recovered the activities of inhibited enzyme–peptide complex. The selection of cooperative peptide pairs will provide a versatile toolkit for modulating enzyme functions, which may potentially be applied to drug discovery and biocatalysis. MDPI 2017-04-26 /pmc/articles/PMC5487955/ /pubmed/28445435 http://dx.doi.org/10.3390/microarrays6020008 Text en © 2017 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fu, Jinglin
Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities
title Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities
title_full Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities
title_fullStr Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities
title_full_unstemmed Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities
title_short Microarray Selection of Cooperative Peptides for Modulating Enzyme Activities
title_sort microarray selection of cooperative peptides for modulating enzyme activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487955/
https://www.ncbi.nlm.nih.gov/pubmed/28445435
http://dx.doi.org/10.3390/microarrays6020008
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