Drug Target Engagement Using Coupled Cellular Thermal Shift Assay-Acoustic Reverse-Phase Protein Array.


Journal

SLAS discovery : advancing life sciences R & D
ISSN: 2472-5560
Titre abrégé: SLAS Discov
Pays: United States
ID NLM: 101697563

Informations de publication

Date de publication:
02 2020
Historique:
pubmed: 31 12 2019
medline: 17 7 2021
entrez: 31 12 2019
Statut: ppublish

Résumé

In the last 5 years, cellular thermal shift assay (CETSA), a technology based on ligand-induced changes in protein thermal stability, has been increasingly used in drug discovery to address the fundamental question of whether drug candidates engage their intended target in a biologically relevant setting. To analyze lysates from cells submitted to increasing temperature, the detection and quantification of the remaining soluble protein can be achieved using quantitative mass spectrometry, Western blotting, or AlphaScreen techniques. Still, these approaches can be time- and cell-consuming. To cope with limitations of throughput and protein amount requirements, we developed a new coupled assay combining the advantages of a nanoacoustic transfer system and reverse-phase protein array technology within CETSA experiments. We validated the technology to assess engagement of inhibitors of insulin-degrading enzyme (IDE), an enzyme involved in diabetes and Alzheimer's disease. CETSA-acoustic reverse-phase protein array (CETSA-aRPPA) allows simultaneous analysis of many conditions and drug-target engagement with a small sample size, in a rapid, cost-effective, and biological material-saving manner.

Identifiants

pubmed: 31885312
doi: 10.1177/2472555219897256
pii: S2472-5552(22)06539-X
doi:

Substances chimiques

Ligands 0
Pharmaceutical Preparations 0
Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

207-214

Auteurs

Adrien Herledan (A)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.

Marine Andres (M)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.
European Genomic Institute for Diabetes, EGID, University of Lille, Lille, France.

Aurore Lejeune-Dodge (A)

Labcyte Inc., San Jose, CA, USA.

Florence Leroux (F)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.
European Genomic Institute for Diabetes, EGID, University of Lille, Lille, France.

Alexandre Biela (A)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.

Catherine Piveteau (C)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.

Sandrine Warenghem (S)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.

Cyril Couturier (C)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.

Benoit Deprez (B)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.
European Genomic Institute for Diabetes, EGID, University of Lille, Lille, France.

Rebecca Deprez-Poulain (R)

University of Lille, Inserm, Institut Pasteur de Lille, U1177-Drugs and Molecules for Living Systems, Lille, France.
European Genomic Institute for Diabetes, EGID, University of Lille, Lille, France.
Institut Universitaire de France (IUF), Paris, France.

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