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Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins

Herein, we report a selection approach to enrich ligands from DNA-encoded libraries (DELs) based on proximity to an enzymatic tag on the target protein. This method involves uncaging or installation of a biotin purification tag on the DNA construct either through photodeprotection of a protected bio...

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Detalles Bibliográficos
Autores principales: Cai, Bo, Mhetre, Amol B., Krusemark, Casey J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811540/
https://www.ncbi.nlm.nih.gov/pubmed/36687357
http://dx.doi.org/10.1039/d2sc05495g
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author Cai, Bo
Mhetre, Amol B.
Krusemark, Casey J.
author_facet Cai, Bo
Mhetre, Amol B.
Krusemark, Casey J.
author_sort Cai, Bo
collection PubMed
description Herein, we report a selection approach to enrich ligands from DNA-encoded libraries (DELs) based on proximity to an enzymatic tag on the target protein. This method involves uncaging or installation of a biotin purification tag on the DNA construct either through photodeprotection of a protected biotin group using a light emitting protein tag (nanoluciferase) or by acylation using an engineered biotin ligase (UltraID). This selection does not require purification of the target protein and results in improved recovery and enrichment of DNA-linked ligands. This approach should serve as a general and convenient tool for molecular discovery with DELs.
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spelling pubmed-98115402023-01-20 Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins Cai, Bo Mhetre, Amol B. Krusemark, Casey J. Chem Sci Chemistry Herein, we report a selection approach to enrich ligands from DNA-encoded libraries (DELs) based on proximity to an enzymatic tag on the target protein. This method involves uncaging or installation of a biotin purification tag on the DNA construct either through photodeprotection of a protected biotin group using a light emitting protein tag (nanoluciferase) or by acylation using an engineered biotin ligase (UltraID). This selection does not require purification of the target protein and results in improved recovery and enrichment of DNA-linked ligands. This approach should serve as a general and convenient tool for molecular discovery with DELs. The Royal Society of Chemistry 2022-11-15 /pmc/articles/PMC9811540/ /pubmed/36687357 http://dx.doi.org/10.1039/d2sc05495g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Cai, Bo
Mhetre, Amol B.
Krusemark, Casey J.
Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins
title Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins
title_full Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins
title_fullStr Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins
title_full_unstemmed Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins
title_short Selection methods for proximity-dependent enrichment of ligands from DNA-encoded libraries using enzymatic fusion proteins
title_sort selection methods for proximity-dependent enrichment of ligands from dna-encoded libraries using enzymatic fusion proteins
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811540/
https://www.ncbi.nlm.nih.gov/pubmed/36687357
http://dx.doi.org/10.1039/d2sc05495g
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