Visualization of clustered protocadherin neuronal self-recognition complexes
Name
nihms-1023915.pdf
Description
Accepted version
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2.12 MB
Format
Adobe PDF
Checksum (MD5)
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Author(s)
Brasch, Julia
Goodman, Kerry M.
Noble, Alex J.
Rapp, Micah
Mannepalli, Seetha
Bahna, Fabiana
Dandey, Venkata P.
Bepler, Tristan
Berger Leighton, Bonnie
Maniatis, Tom
Date Issued
April 10, 2019
Journal
Nature
Publisher
Springer Science and Business Media LLC
Citation
Brasch, J., et al. "Visualization of clustered protocadherin neuronal self-recognition complexes." Nature 569, 7755 (May 2019): 280–283 © 2019 Springer Nature Limited
Version
Author's final manuscript
Abstract
Neurite self-recognition and avoidance are fundamental properties of all nervous systems. These processes facilitate dendritic arborization, prevent formation of autapses and allow free interaction among non-self neurons. Avoidance among self neurites is mediated by stochastic cell-surface expression of combinations of about 60 isoforms of α-, β- and γ-clustered protocadherin that provide mammalian neurons with single-cell identities. Avoidance is observed between neurons that express identical protocadherin repertoires2,5, and single-isoform differences are sufficient to prevent self-recognition10. Protocadherins form isoform-promiscuous cis dimers and isoform-specific homophilic trans dimers. Although these interactions have previously been characterized in isolation, structures of full-length protocadherin ectodomains have not been determined, and how these two interfaces engage in self-recognition between neuronal surfaces remains unknown. Here we determine the molecular arrangement of full-length clustered protocadherin ectodomains in single-isoform self-recognition complexes, using X-ray crystallography and cryo-electron tomography. We determine the crystal structure of the clustered protocadherin γB4 ectodomain, which reveals a zipper-like lattice that is formed by alternating cis and trans interactions. Using cryo-electron tomography, we show that clustered protocadherin γB6 ectodomains tethered to liposomes spontaneously assemble into linear arrays at membrane contact sites, in a configuration that is consistent with the assembly observed in the crystal structure. These linear assemblies pack against each other as parallel arrays to form larger two-dimensional structures between membranes. Our results suggest that the formation of ordered linear assemblies by clustered protocadherins represents the initial self-recognition step in neuronal avoidance, and thus provide support for the isoform-mismatch chain-termination model of protocadherin-mediated self-recognition, which depends on these linear chains. Keywords: cryoelectron tomography; molecular neuroscience; x-ray crystallography
MIT Department
Massachusetts Institute of Technology. Department of Mathematics
Massachusetts Institute of Technology. Computational and Systems Biology Program
Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
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DOI of Published Version
https://doi.org/10.1103/10.1038/s41586-019-1089-3
