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The Surprising Features of the TEAD4‐Vgll1 Protein–Protein Interaction
Author(s) -
Mesrouze Yannick,
Hau Jean Christophe,
Erdmann Dirk,
Zimmermann Catherine,
Fontana Patrizia,
Schmelzle Tobias,
Chène Patrick
Publication year - 2014
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.201300715
Subject(s) - hippo signaling pathway , transcription factor , cofactor , plasma protein binding , biology , microbiology and biotechnology , binding site , computational biology , chemistry , biochemistry , signal transduction , enzyme , gene
The Hippo signaling pathway, which controls organ size in animals, is altered in various human cancers. The TEAD transcription factors, the most downstream elements in this pathway, are regulated by different cofactors, such as the Vgll (vestigial‐like) proteins. Having studied the interaction between Vgll1‐derived peptides and human TEAD4, we show that, although it lacks a key secondary structure element required for tight binding by two other TEAD cofactors (YAP and TAZ), Vgll1‐derived peptides bind to TEAD with nanomolar affinity. We identify a β‐strand:loop:α‐helix motif as the minimal Vgll binding site. Finally, we reveal an unexpected difference between mouse and human Vgll1‐derived peptides.