Efficient Generation of Genome-wide Libraries for Protein-ligand Screens Using Gibson Assembly.

Genome-wide library Genomics Gibson assembly High-throughput screen Nanopore sequencing Protozoan Trypanosoma Yeast surface display

Journal

Bio-protocol
ISSN: 2331-8325
Titre abrégé: Bio Protoc
Pays: United States
ID NLM: 101635102

Informations de publication

Date de publication:
20 Nov 2022
Historique:
received: 15 07 2022
revised: 24 08 2022
accepted: 23 09 2022
entrez: 19 12 2022
pubmed: 20 12 2022
medline: 20 12 2022
Statut: epublish

Résumé

Genome-wide screens using yeast or phage displays are powerful tools for identifying protein-ligand interactions, including drug or vaccine targets, ligand receptors, or protein-protein interactions. However, assembling libraries for genome-wide screens can be challenging and often requires unbiased cloning of 10

Identifiants

pubmed: 36532687
doi: 10.21769/BioProtoc.4558
pii: e4558
pmc: PMC9724014
pii:
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

Copyright © 2022 The Authors; exclusive licensee Bio-protocol LLC.

Déclaration de conflit d'intérêts

Competing interests The authors declare that they have no conflicts of interest with the contents of this article.

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Auteurs

Tamara Sternlieb (T)

Institute of Parasitology, McGill University, Ste Anne de Bellevue, QC H9X 3V9, Canada.

Mira Loock (M)

Institute of Parasitology, McGill University, Ste Anne de Bellevue, QC H9X 3V9, Canada.

Mengjin Gao (M)

Institute of Parasitology, McGill University, Ste Anne de Bellevue, QC H9X 3V9, Canada.

Igor Cestari (I)

Institute of Parasitology, McGill University, Ste Anne de Bellevue, QC H9X 3V9, Canada.
Division of Experimental Medicine, McGill University, Montreal, QC, H4A 3J1, Canada.

Classifications MeSH