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Ubiquitin Engineering for Interrogating the Ubiquitin-Proteasome System and Novel Therapeutic Strategies.
Tang, Jason Q; Marchand, Mary M; Veggiani, Gianluca.
Afiliación
  • Tang JQ; Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, 160 College Street, Toronto, ON M5S3E1, Canada.
  • Marchand MM; Department of Molecular Genetics, University of Toronto, 160 College Street, Toronto, ON M5S3E1, Canada.
  • Veggiani G; Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.
Cells ; 12(16)2023 08 21.
Article en En | MEDLINE | ID: mdl-37626927
Protein turnover, a highly regulated process governed by the ubiquitin-proteasome system (UPS), is essential for maintaining cellular homeostasis. Dysregulation of the UPS has been implicated in various diseases, including viral infections and cancer, making the proteins in the UPS attractive targets for therapeutic intervention. However, the functional and structural redundancies of UPS enzymes present challenges in identifying precise drug targets and achieving target selectivity. Consequently, only 26S proteasome inhibitors have successfully advanced to clinical use thus far. To overcome these obstacles, engineered peptides and proteins, particularly engineered ubiquitin, have emerged as promising alternatives. In this review, we examine the impact of engineered ubiquitin on UPS and non-UPS proteins, as well as on viral enzymes. Furthermore, we explore their potential to guide the development of small molecules targeting novel surfaces, thereby expanding the range of druggable targets.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ubiquitina / Complejo de la Endopetidasa Proteasomal Tipo de estudio: Prognostic_studies Idioma: En Revista: Cells Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ubiquitina / Complejo de la Endopetidasa Proteasomal Tipo de estudio: Prognostic_studies Idioma: En Revista: Cells Año: 2023 Tipo del documento: Article País de afiliación: Canadá