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Mutant Exon1 Huntingtin Aggregation is Regulated by T3 Phosphorylation‐Induced Structural Changes and Crosstalk between T3 Phosphorylation and Acetylation at K6
Author(s) -
Chiki Anass,
DeGuire Sean M.,
Ruggeri Francesco S.,
Sanfelice Domenico,
Ansaloni Annalisa,
Wang ZheMing,
Cendrowska Urszula,
Burai Ritwik,
Vieweg Sophie,
Pastore Annalisa,
Dietler Giovanni,
Lashuel Hilal A.
Publication year - 2017
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201611750
Subject(s) - acetylation , phosphorylation , huntingtin , crosstalk , mutant , lysine , chemistry , biochemistry , microbiology and biotechnology , semisynthesis , amino acid , biology , gene , physics , optics
Herein, we used protein semisynthesis to investigate, for the first time, the effect of lysine acetylation and phosphorylation, as well as the crosstalk between these modifications on the structure and aggregation of mutant huntingtin exon1 (Httex1). Our results demonstrate that phosphorylation at T3 stabilizes the α‐helical conformation of the N‐terminal 17 amino acids (Nt17) and significantly inhibits the aggregation of mutant Httex1. Acetylation of single lysine residues, K6, K9 or K15, had no effect on Httex1 aggregation. Interestingly, acetylation at K6, but not at K9 or K15, reversed the inhibitory effect of T3 phosphorylation. Together, our results provide novel insight into the role of Nt17 post‐translational modifications in regulating the structure and aggregation of Httex1 and suggest that its aggregation and possibly its function(s) are controlled by regulatory mechanisms involving crosstalk between different PTMs.