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JOURNAL ARTICLE
RESEARCH SUPPORT, NON-U.S. GOV'T
A genetically selected cyclic peptide inhibitor of BCL6 homodimerization.
Bioorganic & Medicinal Chemistry 2018 July 16
We report an inhibitor of the homodimeric protein-protein interaction of the BCL6 oncoprotein, identified from a genetically encoded SICLOPPS library of 3.2 million cyclic hexapeptides in combination with a bacterial reverse two-hybrid system. This cyclic peptide is shown to bind the BTB domain of BCL6, disrupts its homodimerization, and subsequent binding of the SMRT2 corepressor peptide.
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