Click and Release Chemistry for Activity-Based Purification of β-Lactam Targets.


Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
17 May 2021
Historique:
received: 21 02 2021
pubmed: 2 4 2021
medline: 22 5 2021
entrez: 1 4 2021
Statut: ppublish

Résumé

β-Lactams, the cornerstone of antibiotherapy, inhibit multiple and partially redundant targets referred to as transpeptidases or penicillin-binding proteins. These enzymes catalyze the essential cross-linking step of the polymerization of cell wall peptidoglycan. The understanding of the mechanisms of action of β-lactams and of resistance to these drugs requires the development of reliable methods to characterize their targets. Here, we describe an activity-based purification method of β-lactam targets based on click and release chemistry. We synthesized alkyne-carbapenems with suitable properties with respect to the kinetics of acylation of a model target, the Ldt

Identifiants

pubmed: 33792096
doi: 10.1002/chem.202100653
doi:

Substances chimiques

Anti-Bacterial Agents 0
Carbapenems 0
Penicillin-Binding Proteins 0
Peptidoglycan 0
beta-Lactams 0
Peptidyl Transferases EC 2.3.2.12

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7687-7695

Subventions

Organisme : Ecole doctorale MTCI

Informations de copyright

© 2021 Wiley-VCH GmbH.

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Auteurs

Saidbakhrom Saidjalolov (S)

Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, UMR 8601 CNRS, Université de Paris, 45, rue des saints-pères, Paris, 75006, France.

Emmanuelle Braud (E)

Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, UMR 8601 CNRS, Université de Paris, 45, rue des saints-pères, Paris, 75006, France.

Zainab Edoo (Z)

INSERM UMRS 1138, Sorbonne Universités, UPMC Univ Paris 06, Sorbonne Paris Cité, Université de Paris, Centre de recherche des Cordeliers, Paris, 75006, France.

Laura Iannazzo (L)

Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, UMR 8601 CNRS, Université de Paris, 45, rue des saints-pères, Paris, 75006, France.

Filippo Rusconi (F)

PAPPSO, Université Paris-Saclay, INRAE, CNRS, AgroParisTech GQE - Le Moulon, Gif-sur-Yvette, 91190, France.

Margaux Riomet (M)

Université Paris Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, 91191, France.

Antoine Sallustrau (A)

Université Paris Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, 91191, France.

Frédéric Taran (F)

Université Paris Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, 91191, France.

Michel Arthur (M)

INSERM UMRS 1138, Sorbonne Universités, UPMC Univ Paris 06, Sorbonne Paris Cité, Université de Paris, Centre de recherche des Cordeliers, Paris, 75006, France.

Matthieu Fonvielle (M)

INSERM UMRS 1138, Sorbonne Universités, UPMC Univ Paris 06, Sorbonne Paris Cité, Université de Paris, Centre de recherche des Cordeliers, Paris, 75006, France.

Mélanie Etheve-Quelquejeu (M)

Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, UMR 8601 CNRS, Université de Paris, 45, rue des saints-pères, Paris, 75006, France.

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