Semi‐Synthetic LC3‐Interacting Degrader for Visualizing Macroautophagic Activity and Targeted Degradation
Macroautophagy is central to cellular homeostasis and emerges as a promising avenue for targeted degradation. However, there is still a lack of efficient approaches allowing for visualizing macroautophagic flux and degradation. Here we develop a semi-synthetic LC3-interacting degrader (SLID) that enables fluorogenic imaging of macroautophagic activities and visualization of targeted degradation. SLID is engineered by fusing LC3-interacting regions (LIRs) to a self-labeling tag and an oligomeric motif, with the LIRs for binding to autophagosomes, the oligomeric motif for enhancing the binding, and the self-labeling tag for visualizing autophagosome formation using a pH indicator. SLID is further coupled to an antibody domain through a dimerization-induced proximity system, allowing chemically inducible degradation of target proteins. We show that this SLID platform permits efficient degradation of diverse target proteins such as disease-associated aggregation-prone proteins and phase-separated condensates. SLID also reveals elevated macroautophagic activities in senescent cells, and is repurposed for inducing senescent cell apoptosis via degradation of pro-survival and anti-apoptotic proteins. Our study highlights the great promise of SLID as a versatile tool for studying macroautophagy and targeted protein degradation.
Authors
- Jian‐Hui Jiang (ORCID: https://orcid.org/0000-0003-1594-4023)
- Fenglin Wang (ORCID: https://orcid.org/0000-0002-5872-2693)
- Xia Chu (ORCID: https://orcid.org/0000-0002-4120-6131)
- Li‐Juan Tang (ORCID: https://orcid.org/0000-0002-2548-1686)
- Keke Zhang (ORCID: https://orcid.org/0000-0003-0836-3802)
- Ji Cheng
- Jing‐Yi Zhang
Institutions
- Hunan University (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-08-26
- DOI
- https://doi.org/10.1002/anie.7042721
- Primary Topic
- Autophagy in Disease and Therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China