Literature DB >> 31200860

Targeted protein degradation mechanisms.

Yi Zhang1, Christine Loh1, Jesse Chen1, Nello Mainolfi2.   

Abstract

Targeted protein degradation mediated by small molecule degraders represents an exciting new therapeutic opportunity to eliminate disease-causing proteins. These molecules recruit E3 ubiquitin ligases to the protein of interest and mediate its ubiquitination and subsequent proteolysis by the proteasome. Significant advancements have been made in the discovery and development of clinically relevant degraders. In this review we will focus on the recent progress in understanding ternary complex formation and structures, ubiquitination, and other critical factors that govern the efficiency of degraders both in vitro and in vivo. With deeper knowledges of these areas, the field is building guiding principles to reduce the level of empiricism and to identify therapeutically relevant degraders more rationally and efficiently.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Mesh:

Year:  2019        PMID: 31200860     DOI: 10.1016/j.ddtec.2019.01.001

Source DB:  PubMed          Journal:  Drug Discov Today Technol        ISSN: 1740-6749


  11 in total

Review 1.  Emerging modes-of-action in drug discovery.

Authors:  Eric Valeur; Frank Narjes; Christian Ottmann; Alleyn T Plowright
Journal:  Medchemcomm       Date:  2019-06-25       Impact factor: 3.597

Review 2.  Recent Developments in PROTAC-Mediated Protein Degradation: From Bench to Clinic.

Authors:  Zhenyi Hu; Craig M Crews
Journal:  Chembiochem       Date:  2021-09-23       Impact factor: 3.461

3.  Modeling the Degradation Effects of Autophagosome Tethering Compounds.

Authors:  Hang Zhang; Ping An; Yiyan Fei; Boxun Lu
Journal:  Neurosci Bull       Date:  2020-09-07       Impact factor: 5.203

4.  A blocking peptide stabilizes lysophosphatidic acid receptor 1 and promotes lysophosphatidic acid-induced cellular responses.

Authors:  Sarah J Taleb; Jianxin Wei; Rachel K Mialki; Su Dong; Yanhui Li; Jing Zhao; Yutong Zhao
Journal:  J Cell Biochem       Date:  2021-04-13       Impact factor: 4.429

Review 5.  Current strategies for the design of PROTAC linkers: a critical review.

Authors:  Robert I Troup; Charlene Fallan; Matthias G J Baud
Journal:  Explor Target Antitumor Ther       Date:  2020-10-30

6.  1,4-dihydropyridine derivatives increase mRNA expression of Psma3, Psmb5, and Psmc6 in rats.

Authors:  Kristīne Dišlere; Evita Rostoka; Egils Bisenieks; Gunars Duburs; Natalia Paramonova; Nikolajs Sjakste
Journal:  Arh Hig Rada Toksikol       Date:  2021-06-28       Impact factor: 2.078

Review 7.  Impact of Cross-Coupling Reactions in Drug Discovery and Development.

Authors:  Melissa J Buskes; Maria-Jesus Blanco
Journal:  Molecules       Date:  2020-07-31       Impact factor: 4.411

8.  Developing degraders: principles and perspectives on design and chemical space.

Authors:  Hannah J Maple; Nat Clayden; Anne Baron; Callum Stacey; Robert Felix
Journal:  Medchemcomm       Date:  2019-08-12       Impact factor: 3.597

9.  Understanding the Metabolism of Proteolysis Targeting Chimeras (PROTACs): The Next Step toward Pharmaceutical Applications.

Authors:  Laura Goracci; Jenny Desantis; Aurora Valeri; Beatrice Castellani; Michela Eleuteri; Gabriele Cruciani
Journal:  J Med Chem       Date:  2020-10-07       Impact factor: 7.446

10.  Discovery of an orally active VHL-recruiting PROTAC that achieves robust HMGCR degradation and potent hypolipidemic activity in vivo.

Authors:  Guoshun Luo; Zhenbang Li; Xin Lin; Xinyu Li; Yu Chen; Kun Xi; Maoxu Xiao; Hanlin Wei; Lizhe Zhu; Hua Xiang
Journal:  Acta Pharm Sin B       Date:  2020-11-06       Impact factor: 11.413

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