Dynamic Compound-Dependent Acoustic Transfer to Investigate Inhibitor Reversibility

Automated mechanism of action studies are introducing the need for tailored compound delivery, which can be challenging for standard compound management procedures. Jump dilution assays investigating inhibitor reversibility require compound delivery at specific volumes to assay specific concentrations of 10 × IC50 for each inhibitor. Creating custom-made source plates with unique compound concentrations to dispense a uniform single volume can be prohibitively slow. A broadly applicable tool that enables on-the fly dispensing of variable amounts of stock concentrations was developed using the Acoustic Transfer System (ATS). The Dynamic Transfer Modification Program (DTMP) is an integrated LabVIEW program used to automate customized volume transfers from each well based on compound identity within a given source plate. A jump dilution investigating the time-dependent inhibition of the enzyme dipeptidyl peptidase-4 (DPP4) with multiple inhibitors is described here to demonstrate the delivery of specific volumes of various compounds in a high-throughput manner. The ability to automate this process allows for the characterization of inhibitor reversibility earlier in the drug discovery process, resulting in better informed lead candidate selection.

Medienart:

E-Artikel

Erscheinungsjahr:

2017

Erschienen:

2017

Enthalten in:

Zur Gesamtaufnahme - volume:22

Enthalten in:

SLAS technology - 22(2017), 5 vom: 20. Okt., Seite 485-492

Sprache:

Englisch

Beteiligte Personen:

Nothstein, Jennifer [VerfasserIn]
MacColl, Elisabeth [VerfasserIn]
Zuck, Paul [VerfasserIn]
Cassaday, Jason [VerfasserIn]
Uebele, Victor N [VerfasserIn]
Hermes, Jeffrey D [VerfasserIn]
Homsher, Michelle F [VerfasserIn]

Links:

Volltext

Themen:

ATS (Acoustic Transfer System)
DPP4 (dipeptidyl peptidase-4)
Dipeptidyl Peptidase 4
Dipeptidyl-Peptidase IV Inhibitors
EC 3.4.14.5
Inhibitor reversibility
Journal Article
Jump dilution

Anmerkungen:

Date Completed 20.11.2018

Date Revised 20.11.2018

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1177/2472630316684807

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM26750439X