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顺式和反式二氯二氨铂(II)与核小体核心的结合。

Binding of cis- and trans-dichlorodiammineplatinum(II) to the nucleosome core.

作者信息

Lippard S J, Hoeschele J D

出版信息

Proc Natl Acad Sci U S A. 1979 Dec;76(12):6091-5. doi: 10.1073/pnas.76.12.6091.

Abstract

The binding of the antitumor drug cis-dichlorodiammineplatinum(II) and its inactive trans isomer with the nucleosome core particle has been investigated. Kinetic studies show that platinum binding increases with incubation time, from a few bound platinum atoms per nucleosome core in the first 0.5 hr to 40-50 after 40 hr. There is no crosslinking or dissociation of nucleosome cores upon platinum binding, as revealed by sedimentation velocity measurements. Electrophoresis through 0.1% sodium dodecyl sulfate/18% polyacrylamide gels after platinum binding reveals striking differences in the DNA and protein band patterns for the two isomers. cis-Dichlorodiammineplatinum(II) binds first to the DNA, retarding and spreading its migration in the gel. A comparison study with the 146-base-pair nucleosome core DNA showed the binding to be little affected by the presence of the histone octamer. The trans complex, on the other hand, produces DNA-histone and histone-histone crosslinks that only appear for the cis isomer after long incubation times. The protein-protein crosslinks were reversed by soaking the gel in cyanide solution to form Pt(CN)(4). Subsequent two-dimensional gel electrophoresis revealed that trans-dichlorodiammineplatinum(II) forms specific crosslinks between histone protein pairs H3 and H2a and H2b and H4 in the nucleosome core. The occurrence of DNA-protein crosslinks was demonstrated by treating the platinum/nucleosome core reaction mixtures with a protease or with nucleases prior to electrophoresis and observing changes in the gel patterns. Platinum was located in the gels through autoradiography using (195m)Pt-labeled complexes. This work clearly demonstrates the greater propensity of trans-dichlorodiammineplatinum(II) to form histone-histone and histone-DNA crosslinks compared with the antitumor active cis isomer, which binds first to the DNA and only forms crosslinks to the histones when the nucleosome core is heavily loaded with platinum.

摘要

对抗肿瘤药物顺式二氯二氨合铂(II)及其无活性的反式异构体与核小体核心颗粒的结合情况进行了研究。动力学研究表明,铂的结合量随孵育时间增加,从最初0.5小时每个核小体核心几个结合的铂原子增加到40小时后达到40 - 50个。沉降速度测量结果显示,铂结合后核小体核心没有交联或解离现象。铂结合后通过0.1%十二烷基硫酸钠/18%聚丙烯酰胺凝胶电泳揭示了两种异构体在DNA和蛋白质条带模式上的显著差异。顺式二氯二氨合铂(II)首先与DNA结合,减缓并扩展其在凝胶中的迁移。与146个碱基对的核小体核心DNA的比较研究表明,组蛋白八聚体的存在对这种结合影响很小。另一方面,反式配合物会产生DNA - 组蛋白和组蛋白 - 组蛋白交联,而顺式异构体只有在长时间孵育后才会出现这种交联。通过将凝胶浸泡在氰化物溶液中形成Pt(CN)(4),可以逆转蛋白质 - 蛋白质交联。随后的二维凝胶电泳显示,反式二氯二氨合铂(II)在核小体核心中组蛋白对H3与H2a以及H2b与H4之间形成特定交联。在电泳前用蛋白酶或核酸酶处理铂/核小体核心反应混合物并观察凝胶模式的变化,证明了DNA - 蛋白质交联的存在。使用(195m)Pt标记的配合物通过放射自显影在凝胶中定位铂。这项工作清楚地表明,与具有抗肿瘤活性的顺式异构体相比,反式二氯二氨合铂(II)形成组蛋白 - 组蛋白和组蛋白 - DNA交联的倾向更大,顺式异构体首先与DNA结合,只有当核小体核心大量负载铂时才与组蛋白形成交联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5b/411808/3a9a94a9edc4/pnas00012-0077-a.jpg

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