2. Academic Validation
  3. Mechanism of action for small-molecule inhibitors of triacylglycerol synthesis

Mechanism of action for small-molecule inhibitors of triacylglycerol synthesis

  • Nat Commun. 2023 May 29;14(1):3100. doi: 10.1038/s41467-023-38934-3.
Xuewu Sui 1 2 3,  Kun Wang 1 2,  Kangkang Song 4 5,  Chen Xu 4 5,  Jiunn Song 1 2,  Chia-Wei Lee 1 2,  Maofu Liao # 6 7,  Robert V Farese Jr # 8 9 10 11,  Tobias C Walther # 12 13 14 15 16
Affiliations

Affiliations

  • 1 Department of Molecular Metabolism, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • 2 Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • 3 Department of Biochemistry and Biophysics, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
  • 4 Department of Biochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • 5 Cryo-EM Core Facility, University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • 6 Department of Cell Biology, Harvard Medical School, Boston, MA, USA. liaomf@sustech.edu.cn.
  • 7 School of Life Sciences, Southern University of Science and Technology, Shenzhen, China. liaomf@sustech.edu.cn.
  • 8 Department of Molecular Metabolism, Harvard T.H. Chan School of Public Health, Boston, MA, USA. robert@mskcc.org.
  • 9 Department of Cell Biology, Harvard Medical School, Boston, MA, USA. robert@mskcc.org.
  • 10 Broad Institute of MIT and Harvard, Cambridge, MA, USA. robert@mskcc.org.
  • 11 Cell Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA. robert@mskcc.org.
  • 12 Department of Molecular Metabolism, Harvard T.H. Chan School of Public Health, Boston, MA, USA. twalther@mskcc.org.
  • 13 Department of Cell Biology, Harvard Medical School, Boston, MA, USA. twalther@mskcc.org.
  • 14 Broad Institute of MIT and Harvard, Cambridge, MA, USA. twalther@mskcc.org.
  • 15 Cell Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA. twalther@mskcc.org.
  • 16 Howard Hughes Medical Institute, Boston, MA, USA. twalther@mskcc.org.
  • # Contributed equally.
PMID: 37248213 DOI: 10.1038/s41467-023-38934-3
Abstract

Inhibitors of triacylglycerol (TG) synthesis have been developed to treat metabolism-related diseases, but we know little about their mechanisms of action. Here, we report cryo-EM structures of the TG-synthesis Enzyme acyl-CoA:diacylglycerol Acyltransferase 1 (DGAT1), a membrane bound O-acyltransferase (MBOAT), in complex with two different inhibitors, T863 and DGAT1IN1. Each inhibitor binds DGAT1's fatty acyl-CoA substrate binding tunnel that opens to the cytoplasmic side of the ER. T863 blocks access to the tunnel entrance, whereas DGAT1IN1 extends further into the Enzyme, with an amide group interacting with more deeply buried catalytic residues. A survey of DGAT1 inhibitors revealed that this amide group may serve as a common pharmacophore for inhibition of MBOATs. The inhibitors were minimally active against the related MBOAT acyl-CoA:cholesterol Acyltransferase 1 (ACAT1), yet a single-residue mutation sensitized ACAT1 for inhibition. Collectively, our studies provide a structural foundation for developing DGAT1 and other MBOAT inhibitors.

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