Structural investigation of CDCA3‐Cdh1 protein–protein interactions using in vitro studies and molecular dynamics simulation. (14th February 2023)

• Record Type: Journal Article
• Authors: Barbhuiya, Tabassum Khair; Fisher, Mark; Boittier, Eric D.; Bolderson, Emma; O'Byrne, Kenneth J.; Richard, Derek J.; Adams, Mark Nathaniel; Gandhi, Neha S.
• Is Part Of: Protein science. Volume 32:Number 3(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2023-02-14
• Subjects: anaphase‐promoting complex/cyclosome -- CDCA3 -- Cdh1 -- co‐immunoprecipitation -- molecular dynamics simulation -- pairwise energy decomposition; Proteins -- Periodicals; 572.6
• DOI: 10.1002/pro.4572
• Languages: English
• ISSNs: 0961-8368

Abstract

Abstract: The anaphase‐promoting complex/cyclosome (APC/C) ubiquitin ligase and its cofactor, Cdh1, regulate the expression of several cell‐cycle proteins and their functions during mitosis. Levels of the protein cell division cycle‐associated protein 3 (CDCA3), which is functionally required for mitotic entry, are regulated by APC/C Cdh1 . CDCA3 is an intrinsically disordered protein and contains both C‐terminal KEN box and D‐box recognition motifs, enabling binding to Cdh1. Our previous findings demonstrate that CDCA3 has a phosphorylation‐dependent non‐canonical ABBA‐like motif within the linker region bridging these two recognition motifs and is required for efficient binding to Cdh1. Here, we sought to identify and further characterize additional residues that participate within this ABBA‐like motif using detailed in vitro experiments and in silico modeling studies. We identified the role of H‐bonds, hydrophobic and ionic interactions across the CDCA3 ABBA‐like motif in the linker region between KEN and D‐box motifs. This linker region adopts a well‐defined structure when bound to Cdh1 in the presence of phosphorylation. Upon alanine mutation, the structure of this region is lost, leading to higher flexibility, and alteration in affinities due to binding to alternate sites on Cdh1. Our findings identify roles for the anchoring residues in the non‐canonical ABBA‐like motif to promote binding to the APC/C Cdh1 and regulation of CDCA3 protein levels.