Advances in Combinatorial Chemistry & High Throughput Screening

Author(s): Ye Fang

DOI: 10.2174/9781608057450113010007

Label-Free Cell Phenotypic GPCR Drug Discovery

Pp: 84-129 (46)

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Abstract

SHS investigation development is considered from the geographical and historical viewpoint. 3 stages are described. Within Stage 1 the work was carried out in the Department of the Institute of Chemical Physics in Chernogolovka where the scientific discovery had been made. At Stage 2 the interest to SHS arose in different cities and towns of the former USSR. Within Stage 3 SHS entered the international scene. Now SHS processes and products are being studied in more than 50 countries.

Abstract

G protein-coupled receptors (GPCRs) have been proven to be the largest family of druggable targets in the human genome. Given the importance of GPCRs as drug targets and the de-orphanization of novel targets, GPCRs are likely to remain the frequent targets of many drug discovery programs. Traditionally, molecular assays dominate in the process of GPCR drug discovery and development. With recent advances in instrumentation and pathway deconvolution of GPCR ligand-induced biosensor signatures, label-free biosensor-enabled cell-based assays have become a very active area for GPCR screening. This article reviews the principles, current status and future directions of leading label-free technology platforms for GPCR drug discovery.

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