生物
聚糖
跨膜蛋白
衣原体
糖基化
鞭毛
跨膜结构域
细胞生物学
生物物理学
生物化学
氨基酸
糖蛋白
基因
突变体
受体
作者
Junhao Huang,Hui Tao,Jikun Chen,Shen Yang,Jianlin Lei,Junmin Pan,Chuangye Yan,Nieng Yan
出处
期刊:Cell
[Elsevier]
日期:2024-03-01
卷期号:187 (7): 1733-1744.e12
被引量:5
标识
DOI:10.1016/j.cell.2024.02.037
摘要
Mastigonemes, the hair-like lateral appendages lining cilia or flagella, participate in mechanosensation and cellular motion, but their constituents and structure have remained unclear. Here, we report the cryo-EM structure of native mastigonemes isolated from Chlamydomonas at 3.0 Å resolution. The long stem assembles as a super spiral, with each helical turn comprising four pairs of anti-parallel mastigoneme-like protein 1 (Mst1). A large array of arabinoglycans, which represents a common class of glycosylation in plants and algae, is resolved surrounding the type II poly-hydroxyproline (Hyp) helix in Mst1. The EM map unveils a mastigoneme axial protein (Mstax) that is rich in heavily glycosylated Hyp and contains a PKD2-like transmembrane domain (TMD). Mstax, with nearly 8,000 residues spanning from the intracellular region to the distal end of the mastigoneme, provides the framework for Mst1 assembly. Our study provides insights into the complexity of protein and glycan interactions in native bio-architectures.
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