Structure of the Repulsive Guidance Molecule (RGM)–Neogenin Signaling Hub

Author:

Bell Christian H.1,Healey Eleanor1,van Erp Susan2,Bishop Benjamin1,Tang Chenxiang1,Gilbert Robert J.C.1,Aricescu A. Radu1,Pasterkamp R. Jeroen2,Siebold Christian1

Affiliation:

1. Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.

2. Department of Neuroscience and Pharmacology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, CG Utrecht 3584, Netherlands.

Abstract

RGM Proteins Members of the repulsive guidance molecule (RGM) family of proteins can be secreted or reside on the surface of cells where they bind to the cell surface receptor, neogenin. The RGM proteins are named for their role in axon guidance for developing neurons, but their function is also linked to a range of human diseases, including inflammation, multiple sclerosis, and cancer. Bell et al. (p. 77 ) solved the crystal structures of the external portions of the RGMB protein with portions of neogenin. The structures revealed interactions of dimers of RGMB with neogenin in which ligand binding induced conformational changes that may initiate intracellular signaling from the receptor. RGM proteins contain a site of autocatalytic cleavage that affects secretion of the proteins, and some disease-associated mutations in RGM proteins were clustered at this site.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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