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来自正常人群的血清标本的二维凝胶电泳。

Two-dimensional gel electrophoresis of serum specimens from a normal population.

作者信息

Tracy R P, Currie R M, Young D S

出版信息

Clin Chem. 1982 Apr;28(4 Pt 2):890-9.

PMID:6176364
Abstract

We examined sera from a normal population by two-dimensional gel electrophoresis, to establish the normal pattern of serum proteins and to investigate genetic polymorphisms. With such information in hand, specimens from patients with certain diseases may be readily evaluated. Towards this goal, we optimized the ISO-DALT system (Proc. Natl, Acad, Sci, USA 74: 5421--5425, 1977) for routine phenotyping of alpha 1-antitrypsin, haptoglobin, GC-globulin, alpha 2-HS-glycoprotein, and transferrin, as well as a previously unknown polymorphic protein. We examined the effects of aging the specimens for 2 h at room temperature (no changes) or at -20 degrees C for several months (small changes), as well as serum/plasma differences and the effect of protease inhibitors. Silver-stain methods were modified to allow simultaneous staining of 10 gels, with reasonably good reproducibility of stain intensity. We quantitated silver-stained gels by densitometry of photographic transparencies. Very small samples suffice with this stain (0.5 microL of serum or plasma), allowing the use of "finger-stick" methods instead of venipuncture, yet the patterns are better resolved and easier to read than those for 10-microL specimens processed on gels stained with Coomassie Blue. Our techniques for rapidly removing albumin and IgG allow the investigator to examine areas on the gel that ordinarily are obscured. The region of haptoglobin has been examined by using serum from an ahaptoglobinemic donor. Finally, we present an expanded "normal" map illustrating the composite protein pattern.

摘要

我们通过二维凝胶电泳检测了正常人群的血清,以建立血清蛋白的正常模式并研究基因多态性。掌握这些信息后,就可以很容易地评估某些疾病患者的样本。为了实现这一目标,我们优化了ISO-DALT系统(《美国国家科学院院刊》74: 5421 - 5425, 1977),用于α1-抗胰蛋白酶、触珠蛋白、GC球蛋白、α2-HS糖蛋白和转铁蛋白以及一种先前未知的多态性蛋白的常规表型分析。我们研究了样本在室温下放置2小时(无变化)或在-20℃下放置数月(有微小变化)的影响,以及血清/血浆差异和蛋白酶抑制剂的作用。对银染方法进行了改进,以便能同时对10块凝胶进行染色,染色强度的重现性相当好。我们通过对摄影透明片进行光密度测定来对银染凝胶进行定量。这种染色只需极少量的样本(0.5微升血清或血浆),这使得可以使用“指尖采血”方法而非静脉穿刺,而且与用考马斯亮蓝染色的凝胶上处理的10微升样本相比,图谱的分辨率更高且更易于解读。我们快速去除白蛋白和IgG的技术使研究人员能够检测凝胶上通常被遮盖的区域。已使用无触珠蛋白血症供体的血清对触珠蛋白区域进行了检测。最后,我们展示了一张扩展的“正常”图谱,阐明了复合蛋白模式。

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