4.8 Article

Crystal Structure of the Human Cannabinoid Receptor CB1

期刊

CELL
卷 167, 期 3, 页码 750-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2016.10.004

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资金

  1. Ministry of Science and Technology of China [2014CB910400, 2015CB910104]
  2. National Nature Science Foundation of China [31330019]
  3. National Institutes of Health [P01DA009158, R37DA023142, R01AI118985]
  4. NSF
  5. Shanghai Municipal Government
  6. ShanghaiTech University
  7. GPCR Consortium
  8. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  9. Cloning, Cell Expression, and Protein Purification Core Facilities of iHuman Institute

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Cannabinoid receptor 1 (CB1) is the principal target of Delta(9)-tetrahydrocannabinol (THC), a psychoactive chemical from Cannabis sativa with a wide range of therapeutic applications and a long history of recreational use. CB1 is activated by endocannabinoids and is a promising therapeutic target for pain management, inflammation, obesity, and substance abuse disorders. Here, we present the 2.8 angstrom crystal structure of human CB1 in complex with AM6538, a stabilizing antagonist, synthesized and characterized for this structural study. The structure of the CB1-AM6538 complex reveals key features of the receptor and critical interactions for antagonist binding. In combination with functional studies and molecular modeling, the structure provides insight into the binding mode of naturally occurring CB1 ligands, such as THC, and synthetic cannabinoids. This enhances our understanding of the molecular basis for the physiological functions of CB1 and provides new opportunities for the design of next-generation CB1-targeting pharmaceuticals.

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