Open AccessNovel protein contact points among TP53 and minichromosome maintenance complex proteins 2, 3, and 5
Author(s) -
SchaeferRamadan Stephanie,
Aleksic Jovana,
AlThani Nayra M.,
Malek Joel A.
Publication year - 2022
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.4805
Subject(s) - interactome , minichromosome maintenance , computational biology , biology , protein–protein interaction , cancer , microbiology and biotechnology , gene , cell cycle , genetics , control of chromosome duplication
Objective Identify protein contact points between TP53 and minichromosome maintenance (MCM) complex proteins 2, 3, and 5 with high resolution allowing for potential novel Cancer drug design. Methods A next‐generation sequencing‐based protein–protein interaction method developed in our laboratory called AVA‐Seq was applied to a gold‐standard human protein interaction set. Proteins including TP53, MCM2, MCM3, MCM5, HSP90AA1, PCNA, NOD1, and others were sheared and ligated into the AVA‐Seq system. Protein–protein interactions were then identified in both mild and stringent selective conditions. Results Known interactions among MCM2, MCM3, and MCM5 were identified with the AVA‐Seq system. The interacting regions detected between these three proteins overlap with the structural data of the MCM complex, and novel domains were identified with high resolution determined by multiple overlapping fragments. Fragments of wild type TP53 were shown to interact with MCM2, MCM3, and MCM5, and details on the location of the interactions were provided. Finally, a mini‐network of known and novel cancer protein interactions was provided, which could have implications for fundamental changes in multiple cancers. Conclusion We provide a high‐resolution mini‐interactome that could direct novel drug targets and implicate possible effects of specific cancer mutations.