Bioorthogonal Aptamer‐ATTEC Conjugates for Degradation of Alpha‐Synuclein via Autophagy‐Lysosomal Pathway

Author:

Liao Xiaofeng12,Qin Geng12,Liu Zhenqi12,Ren Jinsong12,Qu Xiaogang12ORCID

Affiliation:

1. Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun Jilin 130022 P. R. China

2. School of Applied Chemistry and Engineering University of Science and Technology of China Hefei Anhui 230026 P. R. China

Abstract

AbstractAutophagosome‐tethering compound (ATTEC) technology has recently been emerging as a novel approach for degrading proteins of interest (POIs). However, it still faces great challenges in how to design target‐specific ATTEC molecules. Aptamers are single‐stranded DNA or RNA oligonucleotides that can recognize their target proteins with high specificity and affinity. Here, ATTEC is combined with aptamers for POIs degradation. As a proof of concept, pathological protein α‐synuclein (α‐syn) is chosen as the target and an efficient α‐syn degrader is generated. Aptamer as a targeting warhead of α‐syn is conjugated with LC3B‐binding compound 5,7‐dihydroxy‐4‐phenylcoumarin (DP) via bioorthogonal click reaction. It is demonstrated that the aptamer conjugated with DP is capable of clearing α‐syn through LC3 and autophagic degradation. These results indicate that aptamer‐based ATTECs are a versatile approach to degrade POIs by taking advantage of the well‐defined different aptamers for targeting diverse proteins, which provides a new way for the design of ATTECs to degradation of targeted proteins.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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