DNA损伤识别蛋白碘化的后标记技术。

Cancer biochemistry biophysics Pub Date : 1995-01-01
P C Billings, J E Cryer, L Y Moy, B N Engelsberg
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引用次数: 0

摘要

近年来,在了解哺乳动物细胞的核苷酸切除修复途径方面取得了重大进展。虽然引发这一过程的信号事件尚不清楚,但它们可能涉及蛋白质,即损伤识别蛋白(DRPs),它检测特定类型的DNA损伤。在本报告中,我们描述了一种标记DNA损伤识别蛋白的技术。该方法利用碘元素对蛋白质进行放射性碘化,使其与癌症化疗药物顺铂修饰的DNA结合。碘化后,结合蛋白被洗脱并在sds -聚丙烯酰胺凝胶上分析。我们优化了这个过程,使标记反应快速,使用少量的125I。通过这种方法,我们证明了MCF7人乳腺上皮细胞中28和40 kDa的蛋白与CDDP-DNA结合。该技术很敏感,可能有助于鉴定含有少量蛋白质的样品中的DRPs,例如从接受诊断和/或治疗的患者获得的小组织活检标本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A post-labeling technique for the iodination of DNA damage recognition proteins.

Major advances have recently been made in understanding the nucleotide excision repair pathway in mammalian cells. Although the signaling events responsible for initiating this process are not known, they probably involve proteins, i.e., damage recognition proteins (DRPs), which detect specific types of DNA damage. In this report, we describe a technique for labeling DNA damage recognition proteins. The procedure utilizes iodogen to radio-iodinate proteins bound to DNA modified with the cancer chemotherapy drug, cisplatin. Following iodination, bound proteins are eluted and analyzed on SDS-polyacrylamide gels. We have optimized this procedure such that the labeling reactions are rapid and employ small amounts of 125I. Using this procedure, we demonstrate that proteins of 28 and 40 kDa in MCF7 human breast epithelial cells bind to CDDP-DNA. This technique is sensitive and potentially will facilitate the identification of DRPs in samples containing limited amounts of protein, such as small tissue biopsy specimens obtained from patients undergoing diagnostic and/or therapeutic treatment.

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