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PMID: 41797376 已发表 · aheadofprint 英语

The planar cell polarity protein Vangl2 interacts with the PDZ-domains of Scribble but not with a unique PDZ-like domain in Inturned.

FEBS letters ·2026-03-08

Wilmes S, Brysch J, Gelze C, Meier L, Kümmel D

摘要

The proteins Inturned and Fuzzy are members of the tri-longin domain (TLD) RabGEF family and activate the GTPase Rab23 downstream of the core planar cell polarity (PCP) proteins Vangl2 and Prickle. To gain insight into the function of a predicted PDZ domain unique to Inturned among TLD proteins, we performed structural and biochemical characterisations. We show that this domain does not interact with membranes or Vangl2. Instead, we find a phosphorylation-dependent interaction between Vangl2 and a PDZ domain of the apical-basal polarity protein Scribble. A crystal structure of Intu-PDZ reveals a unique PDZ-like fold lacking an interaction site for PDZ-binding motifs. Our data provide new insight into the role of PDZ domains in coordinating cell polarity downstream of Vangl2.

关键词
Intu PDZ domain Scrib Vang X‐ray crystallography protein–protein interaction
文献信息
期刊
FEBS letters
期刊简称
FEBS Lett
ISSN
1873-3468
发表日期
2026-03-08
语言
英语
国家/地区
England
NLM ID
0155157
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