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从含有乙型肝炎抗原的血浆中大规模分离丹氏颗粒,并证明环状双链DNA分子直接从其核心中挤出。

Large-scale isolation of Dane particles from plasma containing hepatitis B antigen and deomnstration of circular double-stranded DNA molecule extruding directly from their cores.

作者信息

Takahashi T, Nakagawa S, Hashimoto T, Takahashi K, Imai M

出版信息

J Immunol. 1976 Oct;117(4):1392-7.

PMID:977955
Abstract

A method was developed to isolate, on a large scale, Dane particles from five liters of pooled plasma of asymptomatic carriers of hepatitis B antigen. It involved three successive ultracentrifugation procedures; the final preparation was more than 98% pure in Dane particles. Purified Dane particles had the density of 1.23 to 1.24 g/cm3. The concentration of nucleic acids in the preparation containing purified Dane particles was too low to be detected either by chemical or by spectrophotometric method. However, a circular double-stranded DNA molecule extruding directly from the core of Dane particles was clearly demonstrated by elelctron microscopic observations. The cores of Dane particles (hepatitis B core antigen; HBCAg) were prepared by treating the Dane particle preparation with mercaptoethanol and Nonidet P-40. They were sufficient both in purity and amounts to allow the determination of antibody to HBCAg by an immune adherence hamagglutination method.

摘要

已研发出一种从5升无症状乙肝抗原携带者混合血浆中大规模分离丹氏颗粒的方法。该方法包括连续三次超速离心程序;最终制备物中丹氏颗粒的纯度超过98%。纯化后的丹氏颗粒密度为1.23至1.24克/立方厘米。含有纯化丹氏颗粒的制剂中核酸浓度过低,无法通过化学方法或分光光度法检测到。然而,通过电子显微镜观察清楚地证实了从丹氏颗粒核心直接挤出的环状双链DNA分子。通过用巯基乙醇和诺乃洗涤剂P - 40处理丹氏颗粒制剂来制备丹氏颗粒核心(乙肝核心抗原;HBCAg)。它们在纯度和数量上都足以通过免疫粘连血凝法测定抗HBCAg抗体。

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