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Review
. 2010 Sep;12(3):378-84.
doi: 10.1208/s12248-010-9198-9. Epub 2010 May 6.

Deorphanization of novel peptides and their receptors

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Review

Deorphanization of novel peptides and their receptors

Akihiko Ozawa et al. AAPS J. 2010 Sep.

Abstract

Peptide hormones and neuropeptides play important roles in endocrine and neural signaling, often using G protein-coupled receptor (GPCR)-mediated signaling pathways. However, the rate of novel peptide discovery has slowed dramatically in recent years. Genomic sequencing efforts have yielded a large number of cDNA sequences that potentially encode novel candidate peptide precursors, as well as hundreds of orphan GPCRs with no known cognate ligands. The complexity of peptide signaling is further highlighted by the requirement for specific posttranslational processing steps, and these must be accomplished in vitro prior to testing newly discovered peptide precursor candidates in receptor assays. In this review, we present historic as well as current approaches to peptide discovery and GPCR deorphanization. We conclude that parallel and combinatorial discovery methods are likely to represent the most fruitful avenues for both peptide discovery as well as for matching the remaining GPCRs with their peptide ligands.

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Fig. 1
Fig. 1
Workflow for generating known and novel peptides products

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References

    1. Steiner DF. The proprotein convertases. Curr Opin Chem Biol. 1998;2:31–9. doi: 10.1016/S1367-5931(98)80033-1. - DOI - PubMed
    1. Nakayama K. Furin: a mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins. Biochem J. 1997;327(Pt 3):625–35. - PMC - PubMed
    1. Mains RE, Berard CA, Denault JB, Zhou A, Johnson RC, Leduc R. PACE4: a subtilisin-like endoprotease with unique properties. Biochem J. 1997;321(Pt 3):587–93. - PMC - PubMed
    1. Smeekens ST, Steiner DF. Identification of a human insulinoma cDNA encoding a novel mammalian protein structurally related to the yeast dibasic processing protease Kex2. J Biol Chem. 1990;265:2997–3000. - PubMed
    1. Seidah NG, Gaspar L, Mion P, Marcinkiewicz M, Mbikay M, Chretien M. cDNA sequence of two distinct pituitary proteins homologous to Kex2 and furin gene products: tissue-specific mRNAs encoding candidates for pro-hormone processing proteinases. DNA Cell Biol. 1990;9:789. doi: 10.1089/dna.1990.9.789. - DOI - PubMed

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