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用于碳二亚胺修饰DNA的免疫测定——超螺旋ColE1 DNA中解链转变的检测

Immunoassays for carbodiimide modified DNA-detection of unpairing transitions in supercoiled ColE1 DNA.

作者信息

Wani A A, Sullivan J K, Lebowitz J

机构信息

Department of Radiology, Ohio State University, Columbus 43210.

出版信息

Nucleic Acids Res. 1989 Dec 11;17(23):9957-77. doi: 10.1093/nar/17.23.9957.

Abstract

The water soluble reagent N-cyclohexyl-N'-beta-(4-methylmorpholinium) ethyl carbodiimide-p-toluene sulphonate (CMC) can be used to probe for unpaired and mismatched sites in DNA. Polyclonal antibodies for CMC modified DNA were produced in order to develop immunological assays for the localization and quantitation of CMC adducts. Immunoslot blot analysis of modified DNA exhibited antibody binding proportional to the extent of CMC modification with adduct detection in the femtamole range. Unmodified DNA did not cross react under the conditions of the assay. The distribution of CMC reactivity for supercoiled ColE1 DNA modified at 100, 200 and 300 mM NaCl was determined by immunoanalysis of EcoRI-Hae2-NruI restriction fragments Southern transferred to nylon membranes. Reactivity above random expectation occurred in the A2-II fragment which can be accounted for by its high A-T content of 71.3%. Reactivity below random expectation occurred in the C fragment which can be accounted for by its low AT content of 43%. CMC modification for the other restriction fragments appeared random.

摘要

水溶性试剂N-环己基-N'-β-(4-甲基吗啉鎓)乙基碳二亚胺对甲苯磺酸盐(CMC)可用于探测DNA中的未配对和错配位点。为了开发用于CMC加合物定位和定量的免疫分析方法,制备了针对CMC修饰DNA的多克隆抗体。对修饰DNA的免疫印迹分析显示,抗体结合与CMC修饰程度成正比,加合物检测范围为飞摩尔级。在该分析条件下,未修饰的DNA不发生交叉反应。通过对转移到尼龙膜上的EcoRI-Hae2-NruI限制片段进行免疫分析,确定了在100、200和300 mM NaCl条件下修饰的超螺旋ColE1 DNA的CMC反应性分布。在A2-II片段中出现了高于随机预期的反应性,这可以归因于其71.3%的高A-T含量。在C片段中出现了低于随机预期的反应性,这可以归因于其43%的低A-T含量。其他限制片段的CMC修饰似乎是随机的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e444/335225/e5dbc2331c9a/nar00140-0447-a.jpg

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