KuINins as a New Class of HIV-1 Inhibitors That Block Post-Integration DNA Repair

被引:3
作者
Anisenko, Andrey [1 ,2 ,3 ]
Galkin, Simon [2 ]
Mikhaylov, Andrey A. [4 ]
Khrenova, Maria G. [1 ,5 ]
Agapkina, Yulia [1 ,3 ]
Korolev, Sergey [1 ,3 ]
Garkul, Lidia [2 ]
Shirokova, Vasilissa [4 ,6 ]
Ikonnikova, Viktoria A. [4 ,6 ]
Korlyukov, Alexander [7 ,8 ,9 ]
Dorovatovskii, Pavel [10 ]
Baranov, Mikhail [4 ,8 ,9 ]
Gottikh, Marina [2 ,3 ]
机构
[1] Lomonosov Moscow State Univ, Chem Dept, Moscow 119992, Russia
[2] Lomonosov Moscow State Univ, Fac Bioengn & Bioinformat, Moscow 119992, Russia
[3] Lomonosov Moscow State Univ, Belozersky Inst Physico Chem Biol, Moscow 119992, Russia
[4] Russian Acad Sci, Shemyakin Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
[5] Russian Acad Sci, Fed Res Ctr Biotechnol, Moscow 119071, Russia
[6] DI Mendeleev Univ Chem Technol Russia, Higher Chem Coll, Moscow 125047, Russia
[7] Nesmeyanov Inst Organoelement Cpds, Moscow 119334, Russia
[8] Pirogov Russian Natl Res Med Univ, Inst Translat Med, Moscow 117997, Russia
[9] Pirogov Russian Natl Res Med Univ, Inst Pharm & Med Chem, Moscow 117997, Russia
[10] Kurchatov Inst, Natl Res Ctr, Moscow 123098, Russia
基金
俄罗斯科学基金会;
关键词
HIV-1; integrase; Ku70; DNA-PK; post-integration repair; inhibitor of protein-protein interaction; KuINins; SMALL-MOLECULE INHIBITORS; LEDGF/P75; REPLICATION; DAMAGE; SITE; REVEALS; POTENT; H2AX; CELL; ATM;
D O I
10.3390/ijms242417354
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Integration of HIV-1 genomic cDNA results in the formation of single-strand breaks in cellular DNA, which must be repaired for efficient viral replication. Post-integration DNA repair mainly depends on the formation of the HIV-1 integrase complex with the Ku70 protein, which promotes DNA-PK assembly at sites of integration and its activation. Here, we have developed a first-class inhibitor of the integrase-Ku70 complex formation that inhibits HIV-1 replication in cell culture by acting at the stage of post-integration DNA repair. This inhibitor, named s17, does not affect the main cellular function of Ku70, namely its participation in the repair of double-strand DNA breaks through the non-homologous end-joining pathway. Using a molecular dynamics approach, we have constructed a model for the interaction of s17 with Ku70. According to this model, the interaction of two phenyl radicals of s17 with the L76 residue of Ku70 is important for this interaction. The requirement of two phenyl radicals in the structure of s17 for its inhibitory properties was confirmed using a set of s17 derivatives. We propose to stimulate compounds that inhibit post-integration repair by disrupting the integrase binding to Ku70 KuINins.
引用
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页数:16
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