生物化学与生物物理进展
生物化學與生物物理進展
생물화학여생물물리진전
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS
2009年
5期
592-600
,共9页
张小轶%何红秋%刘斌%王存新
張小軼%何紅鞦%劉斌%王存新
장소질%하홍추%류빈%왕존신
耐药性%HIV-1整合酶%分子动力学
耐藥性%HIV-1整閤酶%分子動力學
내약성%HIV-1정합매%분자동역학
drug resistance%HIV-1 integrase%MD simulation
二酮酸类化合物(DKAs)是目前最有前景的HIV-1整合酶(integrase,IN)抑制剂.为了解DKAs引起的多种耐药株共有的耐药性机理,选择3种S-1360引起的IN耐药突变体,用分子对接和分子动力学模拟,研究了野生型和突变型IN与S-1360的结合模式,基于该结合模式探讨了3种耐药突变体所共有的耐药性机理.结果表明:在突变体中,S-1360结合到耐药突变IN核心区中的位置靠近功能loop 3区却远离与DNA结合的关键残基,结合位置不同导致S-1360的抑制作用部分丧失;残基138到166区域的柔性对IN发挥生物学功能很重要,S-1360能与DNA结合的关键残基N155及K159形成氢键,这2个氢键作用降低了该区域的柔性,突变体中无类似氢键,因而该区域柔性增高;在突变体中,S-1360的苯环远离病毒DNA结合区,不能阻止病毒DNA末端暴露给宿主DNA;T66I突变导敛残基Ⅰ的长侧链占据IN的活性口袋,阻止抑制剂以与野生型中相同的方式结合到活性中心,这均是产生抗药性的重要原因.这些模拟结果与实验结果吻合,可为抗IN的抑制剂设计和改造提供帮助.
二酮痠類化閤物(DKAs)是目前最有前景的HIV-1整閤酶(integrase,IN)抑製劑.為瞭解DKAs引起的多種耐藥株共有的耐藥性機理,選擇3種S-1360引起的IN耐藥突變體,用分子對接和分子動力學模擬,研究瞭野生型和突變型IN與S-1360的結閤模式,基于該結閤模式探討瞭3種耐藥突變體所共有的耐藥性機理.結果錶明:在突變體中,S-1360結閤到耐藥突變IN覈心區中的位置靠近功能loop 3區卻遠離與DNA結閤的關鍵殘基,結閤位置不同導緻S-1360的抑製作用部分喪失;殘基138到166區域的柔性對IN髮揮生物學功能很重要,S-1360能與DNA結閤的關鍵殘基N155及K159形成氫鍵,這2箇氫鍵作用降低瞭該區域的柔性,突變體中無類似氫鍵,因而該區域柔性增高;在突變體中,S-1360的苯環遠離病毒DNA結閤區,不能阻止病毒DNA末耑暴露給宿主DNA;T66I突變導斂殘基Ⅰ的長側鏈佔據IN的活性口袋,阻止抑製劑以與野生型中相同的方式結閤到活性中心,這均是產生抗藥性的重要原因.這些模擬結果與實驗結果吻閤,可為抗IN的抑製劑設計和改造提供幫助.
이동산류화합물(DKAs)시목전최유전경적HIV-1정합매(integrase,IN)억제제.위료해DKAs인기적다충내약주공유적내약성궤리,선택3충S-1360인기적IN내약돌변체,용분자대접화분자동역학모의,연구료야생형화돌변형IN여S-1360적결합모식,기우해결합모식탐토료3충내약돌변체소공유적내약성궤리.결과표명:재돌변체중,S-1360결합도내약돌변IN핵심구중적위치고근공능loop 3구각원리여DNA결합적관건잔기,결합위치불동도치S-1360적억제작용부분상실;잔기138도166구역적유성대IN발휘생물학공능흔중요,S-1360능여DNA결합적관건잔기N155급K159형성경건,저2개경건작용강저료해구역적유성,돌변체중무유사경건,인이해구역유성증고;재돌변체중,S-1360적분배원리병독DNA결합구,불능조지병독DNA말단폭로급숙주DNA;T66I돌변도렴잔기Ⅰ적장측련점거IN적활성구대,조지억제제이여야생형중상동적방식결합도활성중심,저균시산생항약성적중요원인.저사모의결과여실험결과문합,가위항IN적억제제설계화개조제공방조.
The drug resistant mutations in human immunodefieiency virus type 1 (HIV-1) are a major impediment to successful highly active antiretrovirai therapy (HAART) and new drug design. In order to understand the drug resistance mechanism of HIV-1 integrase (IN) mutually existed for multiple drug-resistant strains to the most potent IN inhibitors diketo acids (DKAs), three S-1360-resistant HIV-1 strains were selected and molecular docking and molecular dynamics (MD) simulations were performed to obtain the inhibitor binding modes. Based on the binding modes, compelling differences between the wild-type and the 3 mutants for IN have been observed. The results showed that: 1) In the mutants, the inhibitor is close to the funetional loop 3 region but far away from the DNA binding site. Different binding sites lead to the decrease in susceptibility to S-1360 in mutants compared to the wild-type IN. 2) The fluctuations in the region of residues 138~166 are important to the biological function of IN. 2 hydrogen-bonds between S-1360 with residues N155 and K159 restrict the flexibility of the region. Drug resistant mutations result in a lack of the interaction, consequently, the less susceptible to S-1360. 3) In the 3 mutant IN complexes, the benzyl ring of S-1360 is far from the viral DNA binding site, thus, S-1360 can not prevent the end of the viral DNA from exposure to human DNA. 4) After T66I mutation, the long side chain of I occupied the active pocket in the 3 mutants, consequently, the inhibitor could not move into the same binding site or have the same orientation. All the above contribute to drug resistance. These results will be useful for the rational inhibitor modify and design.