2pzx: Difference between revisions

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==Overview==
==Overview==
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.
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.


==About this Structure==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Benzer, S.]]
[[Category: Benzer, S.]]
[[Category: Bjorkman, P.J.]]
[[Category: Bjorkman, P J.]]
[[Category: Delker, S.L.]]
[[Category: Delker, S L.]]
[[Category: Ja, W.W.]]
[[Category: Ja, W W.]]
[[Category: Jr., A.P.West.]]
[[Category: Jr., A P.West.]]
[[Category: Roberts, R.W.]]
[[Category: Roberts, R W.]]
[[Category: gpcr g protein-coupled receptor ectodomain]]
[[Category: gpcr g protein-coupled receptor ectodomain]]
[[Category: signaling protein]]
[[Category: signaling protein]]


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Revision as of 19:34, 21 February 2008

File:2pzx.jpg


2pzx, resolution 3.50Å

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Structure of the methuselah ectodomain with peptide inhibitor

OverviewOverview

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.

About this StructureAbout this Structure

2PZX is a Single protein structure of sequence from Drosophila melanogaster. Full crystallographic information is available from OCA.

ReferenceReference

Extension of Drosophila melanogaster life span with a GPCR peptide inhibitor., Ja WW, West AP Jr, Delker SL, Bjorkman PJ, Benzer S, Roberts RW, Nat Chem Biol. 2007 Jul;3(7):415-9. Epub 2007 Jun 3. PMID:17546039

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