Al Mazid, Mohammad Faysal Shkel, Olha Ryu, Eunteg Kim, Jiwon Shin, Kyung Ho Kim, Yun Kyung Lim, Hyun Suk Lee, Jun-Seok 2024-12-13T02:00:10Z 2024-12-13T02:00:10Z 2024-12-12 2024-12 1554-8929 https://pubs.kist.re.kr/handle/201004/151367 Target protein degradation (TPD) is a promising strategy for catalytic downregulation of target proteins through various cellular proteolytic pathways. Despite numerous reports on novel TPD mechanisms, the discovery of target-specific ligands remains a major challenge. Unlike small-molecule ligands, aptamers offer significant advantages, owing to their SELEX-based systematic screening method. To fully utilize aptamers for TPD, we designed an aptamer and N-degron ensemble system (AptaGron) that circumvents the need for synthetic conjugations between aptamers and proteolysis-recruiting units. In our AptaGron system, a peptide nucleic acid containing an N-degron peptide and a sequence complementary to the aptamer was designed. Using this system, we successfully degraded three target proteins, tau, nucleolin, and eukaryotic initiation factor 4E (eIF4E), which lack specific small-molecule ligands. Our results highlight the potential of the AptaGron approach as a robust platform for targeted protein degradation. English American Chemical Society Aptamer and N-Degron Ensemble (AptaGron) as a Target Protein Degradation Strategy Article 10.1021/acschembio.4c00536 1 ACS Chemical Biology, v.19, no.12, pp.2462 - 2468 ACS Chemical Biology 19 12 2462 2468 N scie scopus 001370339000001 Biochemistry & Molecular Biology Biochemistry & Molecular Biology Article END RULE PATHWAY TAU DISCOVERY KNOCKDOWN PROTAC