首页> 外文OA文献 >Protein-DNA crosslinking in reconstituted nucleohistone, nuclei and whole cells by picosecond UV laser irradiation.
【2h】

Protein-DNA crosslinking in reconstituted nucleohistone, nuclei and whole cells by picosecond UV laser irradiation.

机译:皮秒紫外激光照射在重组的核蛋白,细胞核和整个细胞中进行蛋白质-DNA交联。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A picosecond UV laser was used to cross-link proteins to DNA in nuclei, whole cells and reconstituted nucleohistone. Irradiation of the nucleohistone resulted in crosslinking 15-20% of bound histones to DNA in a very short time (one or several picosecond pulses), the efficiency of crosslinking to single stranded DNA being higher than to double stranded DNA. All histones as well as high mobility group 1 proteins were identified in the covalently linked protein-DNA complexes upon irradiation of isolated nuclei and whole cells. A method is suggested for isolation of crosslinked material from cells and nuclei in amounts sufficient for further analysis. Experiments with reconstituted nucleohistones showed that upon irradiation at a constant dose the efficiency of crosslinking depended on the intensity of the light, thus suggesting a two-quantum process is involved in the reaction.
机译:皮秒紫外线激光用于使蛋白质与细胞核,全细胞和重组核组蛋白中的DNA交联。核组蛋白的照射导致在非常短的时间内(一个或几个皮秒脉冲)将15-20%的结合组蛋白与DNA交联,与单链DNA交联的效率高于与双链DNA的交联效率。在分离的细胞核和全细胞照射后,在共价连接的蛋白质-DNA复合物中鉴定了所有组蛋白以及高迁移率的第1组蛋白质。建议一种从细胞和细胞核中分离出交联物质的方法,其数量足以进行进一步分析。重组核仁蛋白的实验表明,以恒定剂量照射后,交联效率取决于光强度,因此表明该反应涉及两个量子过程。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号