FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Ja, W.W., West, A.P., Delker, S.L., Bjorkman, P.J., Benzer, S., Roberts, R.W. (2007). Extension of Drosophila melanogaster life span with a GPCR peptide inhibitor.  Nat. Chem. Biol. 3(7): 415--419.
FlyBase ID
FBrf0202191
Publication Type
Research paper
Abstract
G protein-coupled receptors (GPCRs) mediate signaling from extracellular ligands to intracellular signal transduction proteins. Methuselah (Mth) is a class B (secretin-like) GPCR, a family typified by their large, ligand-binding, N-terminal extracellular domains. Downregulation of mth increases the life span of Drosophila melanogaster; inhibitors of Mth signaling should therefore enhance longevity. We used mRNA display selection to identify high-affinity (K(d) = 15 to 30 nM) peptide ligands that bind to the N-terminal ectodomain of Mth. The selected peptides are potent antagonists of Mth signaling, and structural studies suggest that they perturb the interface between the Mth ecto- and transmembrane domains. Flies constitutively expressing a Mth antagonist peptide have a robust life span extension, which suggests that the peptides inhibit Mth signaling in vivo. Our work thus provides new life span-extending ligands for a metazoan and a general approach for the design of modulators of this important class of GPCRs.
PubMed ID
PubMed Central ID
PMC2803097 (PMC) (EuropePMC)
Related Publication(s)
Note

Antagonizing Methuselah to extend life span.
Alic and Partridge, 2007, Genome Biol. 8(8): 222 [FBrf0216094]

Methuselah antagonist extends life span.
McGarrigle and Huang, 2007, Nat. Chem. Biol. 3(7): 371--372 [FBrf0201858]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Chem. Biol.
    Title
    Nature Chemical Biology
    Publication Year
    2005-
    ISBN/ISSN
    1552-4450 1552-4469
    Data From Reference
    Genes (1)