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Peptides Mimicking the β7/β8 Loop of HIV-1 Reverse Transcriptase p51 as "Hotspot-Targeted" Dimerization Inhibitors.
ACS Medicinal Chemistry Letters ( IF 3.5 ) Pub Date : 2020-01-24 , DOI: 10.1021/acsmedchemlett.9b00623 Pedro A Sánchez-Murcia 1 , Sonia de Castro 1 , Carlos García-Aparicio 1 , M Angeles Jiménez 2 , Angela Corona 3 , Enzo Tramontano 3 , Nicolas Sluis-Cremer 4 , Luis Menéndez-Arias 5 , Sonsoles Velázquez 1 , Federico Gago 6 , María-José Camarasa 1
ACS Medicinal Chemistry Letters ( IF 3.5 ) Pub Date : 2020-01-24 , DOI: 10.1021/acsmedchemlett.9b00623 Pedro A Sánchez-Murcia 1 , Sonia de Castro 1 , Carlos García-Aparicio 1 , M Angeles Jiménez 2 , Angela Corona 3 , Enzo Tramontano 3 , Nicolas Sluis-Cremer 4 , Luis Menéndez-Arias 5 , Sonsoles Velázquez 1 , Federico Gago 6 , María-José Camarasa 1
Affiliation
A conformationally constrained short peptide designed to target a protein-protein interaction hotspot in HIV-1 reverse transcriptase (RT) disrupts p66-p51 interactions and paves the way to the development of novel RT dimerization inhibitors.
中文翻译:
模仿HIV-1逆转录酶p51的β7/β8环的肽是“热点靶向”二聚化抑制剂。
一种构象受限的短肽,旨在靶向HIV-1逆转录酶(RT)中的蛋白质-蛋白质相互作用热点,破坏了p66-p51相互作用,为新型RT二聚化抑制剂的开发铺平了道路。
更新日期:2020-01-24
中文翻译:
模仿HIV-1逆转录酶p51的β7/β8环的肽是“热点靶向”二聚化抑制剂。
一种构象受限的短肽,旨在靶向HIV-1逆转录酶(RT)中的蛋白质-蛋白质相互作用热点,破坏了p66-p51相互作用,为新型RT二聚化抑制剂的开发铺平了道路。