| Literature DB >> 30692685 |
Jean Quancard1, Theo Klein2,3,4,5, Shan-Yu Fung6,7, Martin Renatus8, Nicola Hughes8, Laura Israël8, John J Priatel6,9, Sohyeong Kang6,9, Michael A Blank10,11, Rosa I Viner10, Jutta Blank8, Achim Schlapbach8, Paul Erbel8, Jayachandran Kizhakkedathu4,9, Frédéric Villard8, René Hersperger8, Stuart E Turvey6,7, Joerg Eder8, Frédéric Bornancin12, Christopher M Overall13,14,15.
Abstract
MALT1 paracaspase is central for lymphocyte antigen-dependent responses including NF-κB activation. We discovered nanomolar, selective allosteric inhibitors of MALT1 that bind by displacing the side chain of Trp580, locking the protease in an inactive conformation. Interestingly, we had previously identified a patient homozygous for a MALT1 Trp580-to-serine mutation who suffered from combined immunodeficiency. We show that the loss of tryptophan weakened interactions between the paracaspase and C-terminal immunoglobulin MALT1 domains resulting in protein instability, reduced protein levels and functions. Upon binding of allosteric inhibitors of increasing potency, we found proportionate increased stabilization of MALT1-W580S to reach that of wild-type MALT1. With restored levels of stable MALT1 protein, the most potent of the allosteric inhibitors rescued NF-κB and JNK signaling in patient lymphocytes. Following compound washout, MALT1 substrate cleavage was partly recovered. Thus, a molecular corrector rescues an enzyme deficiency by substituting for the mutated residue, inspiring new potential precision therapies to increase mutant enzyme activity in other deficiencies.Entities:
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Year: 2019 PMID: 30692685 DOI: 10.1038/s41589-018-0222-1
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 15.040