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Applications of fluorescence and bioluminescence resonance energy transfer to drug discovery at G protein coupled receptors

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 398, 期 1, 页码 167-180

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-010-3823-4

关键词

G protein coupled receptor; Fluorescence resonance energy transfer; Time-resolved fluorescence resonance energy transfer; Bioluminescence resonance energy transfer; High throughput; Arrestin; Drug discovery

资金

  1. Biotechnology and Biosciences Research Council [BB/E006302/1]
  2. Medical Research Council [G0900050]
  3. Biotechnology and Biological Sciences Research Council [BB/E006302/1] Funding Source: researchfish
  4. BBSRC [BB/E006302/1] Funding Source: UKRI
  5. MRC [G0900050] Funding Source: UKRI

向作者/读者索取更多资源

The role of G protein coupled receptors (GPCRs) in numerous physiological processes that may be disrupted or modified in disease makes them key targets for the development of new therapeutic medicines. A wide variety of resonance energy transfer (RET) techniques such as fluorescence RET and bioluminescence RET have been developed in recent years to detect protein-protein interactions in living cells. Furthermore, these techniques are now being exploited to screen for novel compounds that activate or block GPCRs and to search for new, previously undiscovered signaling pathways activated by well-known pharmacologically classified drugs. The high resolution that can be achieved with these RET methods means that they are well suited to study both intramolecular conformational changes in response to ligand binding at the receptor level and intermolecular interactions involving protein translocation in subcellular compartments resulting from external stimuli. In this review we highlight the latest advances in these technologies to illustrate general principles.

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