BOPC1 Enantiomers Preparation and HuR Interaction Study. From Molecular Modeling to a Curious DEEP-STD NMR Application.
ACS Med Chem Lett. 2020 May 14;11(5):883-888
Authors: Volpe SD, Listro R, Parafioriti M, Di Giacomo M, Rossi D, Ambrosio FA, Costa G, Alcaro S, Ortuso F, Hirsch AKH, Vasile F, Collina S
Abstract
The Hu family of RNA-binding proteins plays a crucial role in post-transcriptional processes; indeed, Hu-RNA complexes are involved in various dysfunctions (i.e., inflammation, neurodegeneration, and cancer) and have been recently proposed as promising therapeutic targets. Intrigued by this concept, our research efforts aim at identifying small molecules able to modulate HuR-RNA interactions, with a focus on subtype HuR, upregulated and dysregulated in several cancers. By applying structure-based design, we had already identified racemic trans-BOPC1 as promising HuR binder. In this Letter, we accomplished the enantio-resolution, the assignment of the absolute configuration, and the recognition study with HuR of enantiomerically pure trans-BOPC1. For the first time, we apply DEEP (differential epitope mapping)-STD NMR to study the interaction of BOPC1 with HuR and compare its enantiomers, gaining information on ligand orientation and amino acids involved in the interaction, and thus increasing focus on the in silico binding site model.
Capturing a Dynamic Chaperone–Substrate Interaction Using NMR-Informed Molecular Modeling
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Loi?c Salmon, Logan S. Ahlstrom, Scott Horowitz, Alex Dickson, Charles L. Brooks and James C. A. Bardwell
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.6b02382/20160802/images/medium/ja-2016-02382u_0007.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.6b02382
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[NMR paper] Capturing a dynamic chaperone-substrate interaction using NMR-informed molecular modeling.
Capturing a dynamic chaperone-substrate interaction using NMR-informed molecular modeling.
Capturing a dynamic chaperone-substrate interaction using NMR-informed molecular modeling.
J Am Chem Soc. 2016 Jul 14;
Authors: Salmon L, Ahlstrom LS, Horowitz S, Dickson A, Brooks CL, Bardwell JC
Abstract
Chaperones maintain a healthy proteome by preventing aggregation and by aiding in protein folding. Precisely how chaperones influence the conformational properties of their substrates, however, remains unclear. To achieve a detailed...
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Marcos D. Battistel, Hugo F. Azurmendi, Martin Frank and Daro?n I. Freedberg
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.5b03824/20151015/images/medium/ja-2015-038244_0007.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.5b03824
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