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Nanoplatform-Based Delivery Systems for PROTACs

  • Wenbo Che
  • , Xinlin Wang
  • , Sijin Chen
  • , Mao Du
  • , Wenyu Wang
  • , Dan Liu
  • , Shuai Fan
  • , Zundao Wu
  • , Yi Wu
  • , Yanbo Dong*
  • , Qin Xia*
  • *Corresponding author for this work
  • Beijing Institute of Technology
  • SDSZ International Department
  • Capital Medical University

Research output: Contribution to journalReview articlepeer-review

Abstract

Proteolysis Targeting Chimera (PROTAC) is a bifunctional small molecule composed of a ligand for the target protein, a ligand for an E3 ubiquitin ligase, and a chemical linker. It induces the formation of a ternary complex between the target protein and the E3 ligase, thereby promoting ubiquitination and subsequent proteasomal degradation of the target. As an emerging targeted protein degradation (TPD) strategy, PROTACs offer notable advantages such as rapid action, sustained efficacy, and high selectivity. However, PROTACs encounter significant challenges in in vivo delivery due to their unfavorable physicochemical properties, including high molecular weight, limited membrane permeability, and poor plasma stability. In recent years, the development of nanodelivery platforms has emerged as a promising strategy to overcome these limitations, significantly enhancing the bioavailability and therapeutic efficiency of PROTACs while accelerating their clinical translation and application.

Original languageEnglish
Article numbere70301
JournalDrug Development Research
Volume87
Issue number3
DOIs
Publication statusPublished - May 2026
Externally publishedYes

Keywords

  • E3 ubiquitin ligase
  • PROTACs
  • TPD
  • nanodelivery systems
  • stimuli-responsive nanoplatforms

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