5ELJ: Isoform-specific inhibition of SUMO-dependent protein-protein interactions

Citation:
Abstract
Because protein-protein interactions underpin most biological processes, developing tools that target them to understand their function or to inform the development of therapeutics is an important task. SUMOylation is the posttranslational covalent attachment of proteins in the SUMO family (SUMO-1, SUMO-2, or SUMO-3), and it regulates numerous cellular pathways. SUMOylated proteins are recognized by proteins with SUMO-interaction motifs (SIMs) that facilitate noncovalent interactions with SUMO. We describe the use of the Affimer system of peptide display for the rapid isolation of synthetic binding proteins that inhibit SUMO-dependent protein-protein interactions mediated by SIMs both in vitro and in cells. Crucially, these synthetic proteins did not prevent SUMO conjugation either in vitro or in cell-based systems, enabling the specific analysis of SUMO-mediated protein-protein interactions. Furthermore, through structural analysis and molecular modeling, we explored the molecular mechanisms that may underlie their specificity in interfering with either SUMO-1-mediated interactions or interactions mediated by either SUMO-2 or SUMO-3. Not only will these reagents enable investigation of the biological roles of SUMOylation, but the Affimer technology used to generate these synthetic binding proteins could also be exploited to design or validate reagents or therapeutics that target other protein-protein interactions.
PDB ID: 5ELJDownload
MMDB ID: 144913
PDB Deposition Date: 2015/11/4
Updated in MMDB: 2016/11
Experimental Method:
x-ray diffraction
Resolution: 1.983  Å
Source Organism:
synthetic construct
Similar Structures:
Biological Unit for 5ELJ: monomeric; determined by author
Molecular Components in 5ELJ
Label Count Molecule
Protein (1 molecule)
1
Sumo-affirmer-s2d5
Molecule annotation
* Click molecule labels to explore molecular sequence information.

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