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.
School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
Small. 2024 Feb;20(8):e2306760. doi: 10.1002/smll.202306760. Epub 2023 Oct 11.
Autophagosome-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.
自噬体连接化合物(ATTEC)技术最近作为一种新型的降解靶蛋白(POI)的方法而出现。然而,如何设计靶向特异性的 ATTEC 分子仍然面临巨大的挑战。适体是一种单链 DNA 或 RNA 寡核苷酸,能够以高特异性和亲和力识别其靶蛋白。在这里,ATTEC 与适体结合用于 POI 的降解。作为概念验证,选择病理蛋白 α-突触核蛋白(α-syn)作为靶标,并生成有效的 α-syn 降解剂。通过生物正交点击反应,将作为 α-syn 靶向弹头的适体与 LC3B 结合化合物 5,7-二羟基-4-苯基香豆素(DP)偶联。结果表明,通过 LC3 和自噬降解,与 DP 偶联的适体能有效清除 α-syn。这些结果表明,基于适体的 ATTEC 是一种通过利用针对不同蛋白质的明确不同适体来降解 POI 的多功能方法,为设计靶向蛋白的 ATTEC 降解提供了一种新方法。