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使用链霉亲和素包被的磁珠和生物素化抗体研究DNA损伤的诱导和修复:对紫外线照射的人成纤维细胞特定序列中修复补丁的分析

The use of streptavidin-coated magnetic beads and biotinylated antibodies to investigate induction and repair of DNA damage: analysis of repair patches in specific sequences of uv-irradiated human fibroblasts.

作者信息

Kalle W H, Hazekamp-van Dokkum A M, Lohman P H, Natarajan A T, van Zeeland A A, Mullenders L H

机构信息

MGC-Department of Radiation Genetics and Chemical Mutagenesis, State University of Leiden, The Netherlands.

出版信息

Anal Biochem. 1993 Feb 1;208(2):228-36. doi: 10.1006/abio.1993.1037.

Abstract

A new immunoextraction method using biotinylated antibodies and streptavidin-coated magnetic beads has been developed and applied to study the repair of uv-induced DNA damage in specific DNA sequences. uv-irradiated cells were allowed to carry out DNA repair for various time intervals in the presence of 5-bromodeoxyuridine (BrdU). Purified and restricted DNA was subjected to an immunoextraction method employing an anti-BrdU antibody (alpha Brdu), biotinylated goat antimouse antibodies (G alpha Mbio), and streptavidin-coated polymeric magnetic beads. Separation of BrdU containing DNA was achieved by using a magnetic device. This extraction procedure resulted in two fractions of DNA, i.e., BrdU-containing and non-BrdU-containing DNA. Both fractions were blotted on filters and subsequently hybridized with specific DNA probes to determine the relative amount of defined fragments in the two fractions of DNA. Repair experiments using normal primary human fibroblasts showed no difference in the incorporation of repair label in the active adenosine deaminase gene and the inactive 754 locus during the first 4 h following uv irradiation. After longer repair times the active gene incorporated more repair label than the inactive gene, consistent with the known preferential repair of cyclobutane pyrimidine dimers from active housekeeping genes.

摘要

一种使用生物素化抗体和链霉亲和素包被磁珠的新型免疫提取方法已被开发出来,并应用于研究特定DNA序列中紫外线诱导的DNA损伤修复。在5-溴脱氧尿苷(BrdU)存在的情况下,紫外线照射的细胞被允许进行不同时间间隔的DNA修复。纯化并酶切后的DNA采用抗BrdU抗体(α Brdu)、生物素化山羊抗小鼠抗体(GαMbio)和链霉亲和素包被的聚合物磁珠进行免疫提取。通过使用磁性装置实现了含BrdU的DNA的分离。该提取过程产生了两部分DNA,即含BrdU的DNA和不含BrdU的DNA。将这两部分DNA都点样到滤膜上,随后与特定的DNA探针杂交,以确定这两部分DNA中特定片段的相对含量。使用正常原代人成纤维细胞进行的修复实验表明,在紫外线照射后的前4小时内,活性腺苷脱氨酶基因和无活性的754位点在修复标记掺入方面没有差异。在更长的修复时间后,活性基因比无活性基因掺入了更多的修复标记,这与已知的活性管家基因中环丁烷嘧啶二聚体的优先修复一致。

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