Creation and functional screening of a multi-usepeptide library
Studies of functional interactions between transmembrane proteins such as G-protein-coupled receptors and ligands would benefit from the ability to utilize synthetic molecule libraries. This is realized here by the construction and application of a multi-use combinatorial peptide library (MUPL). Pep...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1994-03, Vol.91 (5), p.1614-1618 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Studies of functional interactions between
transmembrane proteins such as G-protein-coupled receptors and ligands would
benefit from the ability to utilize synthetic molecule libraries. This is
realized here by the construction and application of a multi-use combinatorial
peptide library (MUPL). Peptides are liberated from their supports in a dry
state so that the problem of signal interference due to mixing of peptide
molecules, particularly agonists and antagonists, is avoided. In addition, the
peptides are released from their supports in a controlled manner so that
fractions are available for multiple independent tests, thus eliminating the
need for iterative library analysis and resynthesis. The MUPL concept was
validated with a functional screen which detects agonists to G-protein-coupled
receptors and led to the discovery of new ligands. It is expected that combining
MUPLs with functional assays will enhance both basic scientific research and the
rates of drug discovery and development. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.91.5.1614 |