35
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Crystal Structure of the Human Cannabinoid Receptor CB 1

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          SUMMARY

          Cannabinoid receptor 1 (CB 1) is the principal target of Δ 9-tetrahydrocannabinol (THC), a psychoactive chemical from Cannabis sativa with a wide range of therapeutic applications and a long history of recreational use. CB 1 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 Å crystal structure of human CB 1 in complex with AM6538, a stabilizing antagonist, synthesized and characterized for this structural study. The structure of the CB 1-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 CB 1 ligands, such as THC, and synthetic cannabinoids. This enhances our understanding of the molecular basis for the physiological functions of CB 1 and provides new opportunities for the design of next-generation CB 1-targeting pharmaceuticals.

          Graphical abstract

          Related collections

          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          27 January 2017
          20 October 2016
          20 October 2017
          : 167
          : 3
          : 750-762.e14
          Affiliations
          [1 ]iHuman Institute, ShanghaiTech University, 2F Building 6, 99 Haike Road, Pudong New District, Shanghai 201210, China
          [2 ]National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China
          [3 ]Center for Drug Discovery, Department of Pharmaceutical Sciences; Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA 02115, USA
          [4 ]Departments of Biological Sciences and Chemistry, Bridge Institute, University of Southern California, Los Angeles, CA 90089, USA
          [5 ]Departments of Molecular Therapeutics and Neuroscience, The Scripps Research Institute, Jupiter, FL 33458, USA
          [6 ]University of California, San Diego, La Jolla, CA 92093, USA
          [7 ]Shanghai Institute of Materia Medica, Shanghai 201210, China
          [8 ]GPCR Consortium, San Marcos, CA 92078, USA
          Author notes
          Article
          PMC5322940 PMC5322940 5322940 nihpa821382
          10.1016/j.cell.2016.10.004
          5322940
          27768894
          8d249101-7016-4dd6-9eee-da730398dcaa
          History
          Categories
          Article

          Comments

          Comment on this article