Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub.
Repulsive guidance molecule family members (RGMs) control fundamental and diverse cellular processes, including motility and adhesion, immune cell regulation, and systemic iron metabolism. However, it is not known how RGMs initiate signaling through their common cell-surface receptor, neogenin (NEO1...
Những tác giả chính: | , , , , , , , , |
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Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
2013
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_version_ | 1826289814101557248 |
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author | Bell, C Healey, E van Erp, S Bishop, B Tang, C Gilbert, R Aricescu, A Pasterkamp, R Siebold, C |
author_facet | Bell, C Healey, E van Erp, S Bishop, B Tang, C Gilbert, R Aricescu, A Pasterkamp, R Siebold, C |
author_sort | Bell, C |
collection | OXFORD |
description | Repulsive guidance molecule family members (RGMs) control fundamental and diverse cellular processes, including motility and adhesion, immune cell regulation, and systemic iron metabolism. However, it is not known how RGMs initiate signaling through their common cell-surface receptor, neogenin (NEO1). Here, we present crystal structures of the NEO1 RGM-binding region and its complex with human RGMB (also called dragon). The RGMB structure reveals a previously unknown protein fold and a functionally important autocatalytic cleavage mechanism and provides a framework to explain numerous disease-linked mutations in RGMs. In the complex, two RGMB ectodomains conformationally stabilize the juxtamembrane regions of two NEO1 receptors in a pH-dependent manner. We demonstrate that all RGM-NEO1 complexes share this architecture, which therefore represents the core of multiple signaling pathways. |
first_indexed | 2024-03-07T02:34:38Z |
format | Journal article |
id | oxford-uuid:a85fa5d5-34c5-4103-a077-e038f39d6f8c |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T02:34:38Z |
publishDate | 2013 |
record_format | dspace |
spelling | oxford-uuid:a85fa5d5-34c5-4103-a077-e038f39d6f8c2022-03-27T03:01:09ZStructure of the repulsive guidance molecule (RGM)-neogenin signaling hub.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a85fa5d5-34c5-4103-a077-e038f39d6f8cEnglishSymplectic Elements at Oxford2013Bell, CHealey, Evan Erp, SBishop, BTang, CGilbert, RAricescu, APasterkamp, RSiebold, CRepulsive guidance molecule family members (RGMs) control fundamental and diverse cellular processes, including motility and adhesion, immune cell regulation, and systemic iron metabolism. However, it is not known how RGMs initiate signaling through their common cell-surface receptor, neogenin (NEO1). Here, we present crystal structures of the NEO1 RGM-binding region and its complex with human RGMB (also called dragon). The RGMB structure reveals a previously unknown protein fold and a functionally important autocatalytic cleavage mechanism and provides a framework to explain numerous disease-linked mutations in RGMs. In the complex, two RGMB ectodomains conformationally stabilize the juxtamembrane regions of two NEO1 receptors in a pH-dependent manner. We demonstrate that all RGM-NEO1 complexes share this architecture, which therefore represents the core of multiple signaling pathways. |
spellingShingle | Bell, C Healey, E van Erp, S Bishop, B Tang, C Gilbert, R Aricescu, A Pasterkamp, R Siebold, C Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub. |
title | Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub. |
title_full | Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub. |
title_fullStr | Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub. |
title_full_unstemmed | Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub. |
title_short | Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub. |
title_sort | structure of the repulsive guidance molecule rgm neogenin signaling hub |
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