| Literature DB >> 16846799 |
Abstract
The concepts and philosophies of HTS can be productively applied to the discovery of new biopharmaceuticals. It is now possible, comprehensively and systematically, to enumerate, clone, produce and screen all secreted proteins, by building upon knowledge accumulated over the past two decades in HTS, genomics and parallel protein expression technologies. Each of the crucial operational components (comprehensive and high-quality cDNA library construction, proper protein-sequence classification, high-throughput protein production, medically relevant assays, state-of-the-art screening and data management) must be optimized to increase the chances of success. In this review, we draw comparisons between small-molecule and protein screening to illuminate common underlying principles as well as differences between the two operations.Mesh:
Year: 2006 PMID: 16846799 DOI: 10.1016/j.drudis.2006.06.010
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851