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通过特异性抗体对ColE1 DNA中N-乙酰氧基-N-2-乙酰氨基芴结合位点进行电子显微镜观察。

Electron microscopic visualization of N-acetoxy-N-2-acetylaminofluorene binding sites in ColE1 DNA by means of specific antibodies.

作者信息

de Murcia G, Lang M C, Freund A M, Fuchs R P, Duane M P, Sage E, Leng M

出版信息

Proc Natl Acad Sci U S A. 1979 Dec;76(12):6076-80. doi: 10.1073/pnas.76.12.6076.

Abstract

ColE1 DNA has been allowed to react in vitro with N-acetoxy-N-2-[14C]acetylaminofluorene in the range of 0-15 N-2-[14C]acetylaminofluorene residues bound per molecule of DNA, at the C8 of guanine residues. Purified rabbit antibodies to both N-2-(guanosine-8-yl)-acetylaminofluorene and native DNA that had reacted with N-acetoxy-N-2-acetylaminofluorene were shown by electron microscopy to recognize specifically the acetylaminofluorene-modified ColE1 DNA. The antibodies bound to DNA were visualized either per se or after reaction with goat anti-rabbit immunoglobulins coupled with ferritin. There was a linear relationship between the average number of antibodies bound per DNA molecule and the number of N-2-(deoxyguanosine-8yl)-acetylaminofluorene residues per DNA molecule. The slope of this straight line was equal to 0.4. Due to the bivalence of the immunoglobulins one would expect a value of 0.5; we actually observed an important fraction of the bound antibodies crosslinking two parts of the same (or of another) DNA molecule.

摘要

已使大肠杆菌素E1 DNA在体外与N - 乙酰氧基 - N - 2 - [¹⁴C]乙酰氨基芴反应,反应范围为每分子DNA在鸟嘌呤残基的C8位结合0至15个N - 2 - [¹⁴C]乙酰氨基芴残基。通过电子显微镜显示,针对N - 2 - (鸟苷 - 8 - 基) - 乙酰氨基芴和已与N - 乙酰氧基 - N - 2 - 乙酰氨基芴反应的天然DNA的纯化兔抗体能特异性识别乙酰氨基芴修饰的大肠杆菌素E1 DNA。与DNA结合的抗体本身或与偶联铁蛋白的山羊抗兔免疫球蛋白反应后均可被观察到。每个DNA分子结合的抗体平均数量与每个DNA分子中N - 2 - (脱氧鸟苷 - 8 - 基) - 乙酰氨基芴残基的数量之间存在线性关系。这条直线的斜率等于0.4。由于免疫球蛋白的二价性,预期值为0.5;实际上我们观察到很大一部分结合的抗体使同一(或另一个)DNA分子的两部分发生交联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f36f/411805/e665b210bbce/pnas00012-0061-a.jpg

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