Cited by 204Protein Degradation and InhibitorsUbiquitin and proteasome pathwaysChemical Synthesis and Analysis

Emerging New Concepts of Degrader Technologies

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Ding, Yu, Fei, Yiyan, Lu, Boxun·2020·Trends in Pharmacological Sciences

Abstract

Traditional drug discovery focuses on identifying direct inhibitors of target proteins. This typically relies on a measurable biochemical readout and accessible binding sites whose occupancy influences the function of the target protein. These requirements preclude many disease-causing proteins from being 'druggable' targets, and these proteins are categorized as 'undruggable'. The proteolysis-targeting chimera (PROTAC) technology provides powerful tools to degrade these undruggable targets and has become a promising approach for drug discovery. However, the PROTAC technology has some limitations, and emerging new degrader technologies may greatly broaden the spectrum of targets that could be selectively degraded by harnessing a second major degradation pathway in cells. We review key emerging technologies that exploit the lysosomal degradation pathway and discuss their potential applications and limitations.

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Crossref · 10.1016/j.tips.2020.04.005

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  • The success of PROTACs in hijacking the UPS for TPD has motivated research into other classes of heterobifunctional molecules that depend on non-UPS pathways to degrade a POI.

    “The success of proteolysis-targeting chimeras (PROTACs) in hijacking the ubiquitin–proteasome system (UPS) for targeted protein degradation (TPD) has motivated research into other classes of heterobifunctional molecules that depend on non-UPS pathways to degrade a protein of interest (POI)246,247.”

    From PROTAC targeted protein degraders: the past is prologue (2022) · cites this paper as [246]

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References 77 · Cited by 204

Authors
Ding, Y., Fei, Y., & Lu, B.
Affiliations
  • Shanghai Medical College of Fudan University (CN)
  • Fudan University (CN)
Corresponding author
  • Ding, Yu
  • Fei, Yiyan
  • Lu, Boxun
Venue
Trends in Pharmacological Sciences
Publisher
Elsevier BV
Published
2020-07
Volume
41
Issue
7
Pages
464-474
ISSN
0165-6147 (ISSN-L)
OpenAlex
W3017485915
Cited by
204
References
77
Citations by year
2026: 23 · 2025: 36 · 2024: 32 · 2023: 37 · 2022: 37 · 2021: 34 · 2020: 4
FWCI
2.73
Type
journal article
Language
en
Open access
Locations
  • Trends in Pharmacological Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Natural Science Foundation of China
  • Academy of Medical Sciences
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chemical Synthesis and Analysis
Keywords
PROTACs, undruggable targets, protein degradation, drug discovery, targeted protein degradation
MeSH terms
Humans, Proteins, Technology, Drug Discovery, Proteolysis

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