A scalable strategy to solve structures of PDZ domains and their complexes. Issue 4 (11th March 2022)

• Record Type: Journal Article
• Authors: Cousido-Siah, Alexandra; Carneiro, Laura; Kostmann, Camille; Ecsedi, Peter; Nyitray, Laszlo; Trave, Gilles; Gogl, Gergo
• Is Part Of: Acta crystallographica. Volume 78:Issue 4(2022)
• Page Start: 509
• Page End: 516
• Publication Date: 2022-03-11
• Subjects: PDZ domains -- crystallization chaperones -- AlphaFold; X-ray crystallography -- Periodicals; Crystallography -- Periodicals; Molecular biology -- Periodicals; Molecular structure -- Periodicals; Biomolecules -- Structure -- Periodicals; Cytology -- Periodicals; Biomolecules -- Structure; Crystallography; Cytology; Molecular biology; Molecular structure; X-ray crystallography; Periodicals; 548
• DOI: 10.1107/S2059798322001784
• Languages: English
• ISSNs: 2059-7983

Abstract

Abstract : This article describes a new strategy for the rapid crystallization of PDZ domains using annexin A2 as a crystallization chaperone. Abstract : The human PDZome represents one of the largest globular domain families in the human proteome, with 266 instances. These globular domains typically interact with C‐terminal peptide motifs found in thousands of human proteins. Despite previous efforts, not all PDZ domains have experimentally solved structures and most of their complexes remain to be solved. Here, a simple and cost‐effective strategy is proposed for the crystallization of PDZ domains and their complexes. A human annexin A2 fusion tag was used as a crystallization chaperone and the structures of nine PDZ domains were solved, including five domains that had not yet been solved. Finally, these novel experimental structures were compared with AlphaFold predictions and it is speculated how predictions and experimental methods could cooperate in order to investigate the structural landscapes of entire domain families and interactomes.