Novel Small Molecules Targeting the Intrinsically Disordered Structural Ensemble of a-Synuclein Protect Against Diverse a-Synuclein Mediated Dysfunctions

Tóth, Gergely ; Neumann, Thomas ; Berthet, Amandine ; Masliah, Eliezer ; Spencer, Brian ; Tao, Jiahui ; Jobling, Michael F. ; Gardai, Shyra J. ; Bertoncini, Carlos W. ; Cremades, Nunilo (Universidad de Zaragoza) ; Bova, Michael ; Ballaron, Stephen ; Chen, Xiao-Hua ; Mao, Wenxian ; Nguyen, Phuong ; Tabios, Mariano C. ; Tambe, Mitali A. ; Rochet, Jean-Christophe ; Junker, Hans-Dieter ; Schwizer, Daniel ; Sekul, Renate ; Ott, Inge ; Anderson, John P. ; Szoke, Balazs ; Hoffman, Wherly ; Christodoulou, John ; Yednock, Ted ; Agard, David A. ; Schenk, Dale ; McConlogue, Lisa
Novel Small Molecules Targeting the Intrinsically Disordered Structural Ensemble of a-Synuclein Protect Against Diverse a-Synuclein Mediated Dysfunctions
Resumen: The over-expression and aggregation of α-synuclein (αSyn) are linked to the onset and pathology of Parkinson’s disease. Native monomeric αSyn exists in an intrinsically disordered ensemble of interconverting conformations, which has made its therapeutic targeting by small molecules highly challenging. Nonetheless, here we successfully target the monomeric structural ensemble of αSyn and thereby identify novel drug-like small molecules that impact multiple pathogenic processes. Using a surface plasmon resonance high-throughput screen, in which monomeric αSyn is incubated with microchips arrayed with tethered compounds, we identified novel αSyn interacting drug-like compounds. Because these small molecules could impact a variety of αSyn forms present in the ensemble, we tested representative hits for impact on multiple αSyn malfunctions in vitro and in cells including aggregation and perturbation of vesicular dynamics. We thereby identified a compound that inhibits αSyn misfolding and is neuroprotective, multiple compounds that restore phagocytosis impaired by αSyn overexpression, and a compound blocking cellular transmission of αSyn. Our studies demonstrate that drug-like small molecules that interact with native αSyn can impact a variety of its pathological processes. Thus, targeting the intrinsically disordered ensemble of αSyn offers a unique approach to the development of small molecule research tools and therapeutics for Parkinson’s disease.
Idioma: Inglés
DOI: 10.1038/s41598-019-52598-4
Año: 2019
Publicado en: Scientific Reports 9, 1 (2019), 16947 [14 pp]
ISSN: 2045-2322

Factor impacto JCR: 3.998 (2019)
Categ. JCR: MULTIDISCIPLINARY SCIENCES rank: 17 / 71 = 0.239 (2019) - Q1 - T1
Factor impacto SCIMAGO: 1.341 - Multidisciplinary (Q1)

Tipo y forma: Artículo (Versión definitiva)
Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)

Creative Commons Debe reconocer adecuadamente la autoría, proporcionar un enlace a la licencia e indicar si se han realizado cambios. Puede hacerlo de cualquier manera razonable, pero no de una manera que sugiera que tiene el apoyo del licenciador o lo recibe por el uso que hace.


Exportado de SIDERAL (2020-10-28-13:18:44)


Visitas y descargas

Este artículo se encuentra en las siguientes colecciones:
Artículos



 Registro creado el 2020-10-28, última modificación el 2020-10-28


Versión publicada:
 PDF
Valore este documento:

Rate this document:
1
2
3
 
(Sin ninguna reseña)