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Nanobody inhibitors of Plexin-B1 identify allostery in plexin–semaphorin interactions and signaling

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posted on 2023-09-28, 09:17 authored by R Cowan, M Trokter, A Oleksy, M Fedorova, K Sawmynaden, T Worzfeld, S Offermanns, D Matthews, MD Carr, G Hall

Plexin-B1 is a receptor for the cell surface semaphorin, Sema4D. This signaling system has been implicated in a variety of human diseases, including cancer, multiple sclerosis and osteoporosis. While inhibitors of the Plexin-B1:Sema4D interaction have been previously reported, understanding their mechanism has been hindered by an incomplete structural view of Plexin-B1. In this study, we have raised and characterized a pair of nanobodies that are specific for mouse Plexin-B1 and which inhibit the binding of Sema4D to mouse Plexin-B1 and its biological activity. Structural studies of these nanobodies reveal that they inhibit the binding of Sema4D in an allosteric manner, binding to epitopes not previously reported. In addition, we report the first unbound structure of human Plexin-B1, which reveals that Plexin-B1 undergoes a conformational change on Sema4D binding. These changes mirror those seen upon binding of allosteric peptide modulators, which suggests a new model for understanding Plexin-B1 signaling and provides a potential innovative route for therapeutic modulation of Plexin-B1.

History

Author affiliation

Department of Molecular and Cell Biology, Leicester Institute of Structural and Chemical Biology, University of Leicester

Version

  • VoR (Version of Record)

Published in

Journal of Biological Chemistry

Volume

299

Issue

6

Pagination

104740

Publisher

Elsevier BV

issn

0021-9258

eissn

1083-351X

Copyright date

2023

Available date

2023-09-28

Spatial coverage

United States

Language

eng

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