4.6 Article

A Peptide Derived from G0/G1 Switch Gene 2 Acts as Noncompetitive Inhibitor of Adipose Triglyceride Lipase

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 289, Issue 47, Pages -

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M114.602599

Keywords

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Funding

  1. DK Molecular Enzymology
  2. Wittgenstein Award [Z136]
  3. Austrian Science Fund [P25193]
  4. Fondation Leducq [12CVD04]
  5. [SFB Lipotox F30]
  6. Austrian Science Fund (FWF) [F 3002, W 901, Z 136] Funding Source: researchfish
  7. Austrian Science Fund (FWF) [Z136] Funding Source: Austrian Science Fund (FWF)

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The protein G(0)/G(1) switch gene 2 (G0S2) is a small basic protein that functions as an endogenous inhibitor of adipose triglyceride lipase (ATGL), a key enzyme in intracellular lipolysis. In this study, we identified a short sequence covering residues Lys-20 to Ala-52 in G0S2 that is still fully capable of inhibiting mouse and human ATGL. We found that a synthetic peptide corresponding to this region inhibits ATGL in a noncompetitive manner in the nanomolar range. This peptide is highly selective for ATGL and does not inhibit other lipases, including hormone-sensitive lipase, monoacylglycerol lipase, lipoprotein lipase, and patatin domain-containing phospholipases 6 and 7. Because increased lipolysis is linked to the development of metabolic disorders, the inhibition of ATGL by G0S2-derived peptides may represent a novel therapeutic tool to modulate lipolysis.

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