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Please do not disturb: Destruction of chromatin structure by supravital nucleic acid probes revealed by a novel assay of DNA-histone interaction

机译:请不要打扰:DNA和组蛋白相互作用的新检测揭示了上卵核酸探针对染色质结构的破坏

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摘要

The biomarkers designed to be used supravitally are expected to have minimal effect on structure and function of the cell. Unfortunately nearly all fluorochromes developed to probe live cells interact in undesired way with cellular constituents and affect functional pathways. Herein we comment on potential applications of diverse DNA binding probes in view of the recent article by Wojcik & Dobrucki on DRAQ 5 and SYTO 17. The approach used by these authors to assess DNA-histone interactions using the cells having histones tagged with fluorescent proteins offers a valuable tool to study mechanism of action of antitumor drugs targeting DNA. While the effect of many intercalating drugs may be similar to that of DRAQ5, it may be of particular interest to observe the effects induced by intra-strand and inter-strand DNA crosslinking drugs, alkylating agents, histone deacetylase inhibitors or even anti-metabolites. The cells having histones tagged with fluorescent proteins thus may serve as biomarkers to probe mechanism of action of drugs targeting DNA or affecting chromatin structure. In fact, because such gross chromatin changes as revealed by dissociation and segregation of histones from DNA are most likely incompatible with long-term cell survival, the methodology may be applied for rapid screening of investigational antitumor agents.
机译:设计用于超量使用的生物标志物有望对细胞的结构和功能产生最小的影响。不幸的是,几乎所有用于探测活细胞的荧光染料都以不希望的方式与细胞成分相互作用,并影响功能途径。本文中,鉴于Wojcik&Dobrucki最近在DRAQ 5和SYTO 17上发表的文章,我们评论了各种DNA结合探针的潜在应用。这些作者使用具有荧光蛋白标记的组蛋白的细胞评估DNA-组蛋白相互作用的方法提供了研究靶向DNA的抗肿瘤药物作用机理的一种有价值的工具。尽管许多插层药物的作用可能与DRAQ5相似,但观察由链内和链间DNA交联药物,烷化剂,组蛋白脱乙酰基酶抑制剂或什至抗代谢物诱导的作用可能特别有意义。因此,具有用荧光蛋白标记的组蛋白的细胞可以用作生物标记,以探测靶向DNA或影响染色质结构的药物的作用机理。实际上,由于组蛋白从DNA的解离和分离所揭示的总体染色质变化很可能与长期细胞存活不相容,因此该方法可用于快速筛选研究性抗肿瘤药物。

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