Fine Sampling of Sequence Space for Membrane Protein Structural Biology.
high throughput biology
integral membrane proteins
protein expression
protein purification
structural biology
structural genomics
Journal
Journal of molecular biology
ISSN: 1089-8638
Titre abrégé: J Mol Biol
Pays: Netherlands
ID NLM: 2985088R
Informations de publication
Date de publication:
23 07 2021
23 07 2021
Historique:
received:
26
03
2021
revised:
12
05
2021
accepted:
12
05
2021
pubmed:
23
5
2021
medline:
21
9
2021
entrez:
22
5
2021
Statut:
ppublish
Résumé
We describe an enhancement of traditional genomics-based approaches to improve the success of structure determination of membrane proteins. Following a broad screen of sequence space to identify initial expression-positive targets, we employ a second step to select orthologs with closely related sequences to these hits. We demonstrate that a greater percentage of these latter targets express well and are stable in detergent, increasing the likelihood of identifying candidates that will ultimately yield structural information.
Identifiants
pubmed: 34022208
pii: S0022-2836(21)00273-4
doi: 10.1016/j.jmb.2021.167055
pmc: PMC8286341
mid: NIHMS1706670
pii:
doi:
Substances chimiques
Bacterial Proteins
0
Membrane Proteins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
167055Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM132120
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM098617
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM107462
Pays : United States
Organisme : NIGMS NIH HHS
ID : P41 GM116799
Pays : United States
Organisme : NIGMS NIH HHS
ID : U54 GM095315
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Competing Interests The authors declare no competing interests.
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