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Elife. 2017 Nov 15;6. pii: e27434. doi: 10.7554/eLife.27434.

A recombinant BBSome core complex and how it interacts with ciliary cargo.

Author information

1
Department of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
2
Structural Biology Group, Max Planck Institute of Molecular Physiology, Dortmund, Germany.

Abstract

Cilia are small, antenna-like structures on the surface of eukaryotic cells that harbor a unique set of sensory proteins, including GPCRs and other membrane proteins. The transport of these proteins involves the BBSome, an eight-membered protein complex that is recruited to ciliary membranes by the G-protein Arl6. BBSome malfunction leads to Bardet-Biedl syndrome, a ciliopathy with severe consequences. Short ciliary targeting sequences (CTS) have been identified that trigger the transport of ciliary proteins. However, mechanistic studies that relate ciliary targeting to BBSome binding are missing. Here we used heterologously expressed BBSome subcomplexes to analyze the complex architecture and to investigate the binding of GPCRs and other receptors to the BBSome. A stable heterohexameric complex was identified that binds to GPCRs with interactions that only partially overlap with previously described CTS, indicating a more complex recognition than anticipated. Arl6•GTP does not affect these interactions, suggesting no direct involvement in cargo loading/unloading.

KEYWORDS:

BBSome; E. coli; S.frugiperda; biochemistry; biophysics; ciliary cargo; cilium; human; intraflagellar transport; structural biology

PMID:
29168691
PMCID:
PMC5700813
DOI:
10.7554/eLife.27434
[Indexed for MEDLINE]
Free PMC Article

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