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使用单克隆抗体鉴定、定量和纯化蟑螂过敏原。

Identification, quantitation, and purification of cockroach allergens using monoclonal antibodies.

作者信息

Pollart S M, Mullins D E, Vailes L D, Hayden M L, Platts-Mills T A, Sutherland W M, Chapman M D

机构信息

Department of Medicine, University of Virginia, Charlottesville 22908.

出版信息

J Allergy Clin Immunol. 1991 Feb;87(2):511-21. doi: 10.1016/0091-6749(91)90010-l.

Abstract

A panel of murine IgG monoclonal antibodies (MAbs) was raised against German cockroach (CR) (Blattella germanica) extract and selectively screened to identify MAb directed against allergen(s) recognized by IgE antibodies. Sera from 28 CR-allergic patients were used as sources of IgE antibodies to detect allergens "presented" by the MAb. Four clones (10A6, 3G12, 8F4, and 1D4) produced MAb to allergen(s) that bound IgE antibodies. Quantitative radioimmunoassays were used to compare levels of the MAb-defined allergens in CR extracts. MAb 10A6 reacted with a cross-reacting allergen that was detected in 9/14 CR species, including Blattella, Periplaneta, Blatta, Leucophea, and Supella spp, at concentrations of 100 to 10,000 U/ml. In contrast, MAb 3G12, 8F4, and 1D4 were Blattella specific. The allergen defined by MAb 8F4 was purified by MAb affinity chromatography and size-exclusion by high-performance liquid chromatography. It is a 36 kd heat-sensitive protein, isoelectric point, 5.2 to 5.4. Allergen 10A6 was partially purified by isoelectric focusing and high-performance liquid chromatography. It is a heat-stable, acidic protein (isoelectric point 3.15). Based on comparison of their properties with properties of previously described CR allergens, the allergens defined by MAb 10A6 and 8F4 have been provisionally designated Blattella germanica allergen I (Bla g I) and Blattella germanica allergen II (Bla g II), respectively. Assays of six commercial CR skin test extracts demonstrated a 200-fold difference in Bla g I levels (4.7 to 1085 U/ml) and only two extracts that contained detectable Bla g II (248 and 324 U/ml). The results demonstrate that MAb can be used to identify and define CR allergens and that the strategy of the use of MAb as a first step in allergen analysis and purification can be very effective, especially for poorly characterized allergen extracts.

摘要

制备了一组针对德国小蠊(CR)(德国小蠊)提取物的鼠IgG单克隆抗体(MAb),并进行选择性筛选,以鉴定针对IgE抗体识别的过敏原的单克隆抗体。来自28名CR过敏患者的血清用作IgE抗体来源,以检测单克隆抗体“呈现”的过敏原。四个克隆(10A6、3G12、8F4和1D4)产生了与结合IgE抗体的过敏原的单克隆抗体。使用定量放射免疫测定法比较CR提取物中由单克隆抗体定义的过敏原水平。单克隆抗体10A6与一种交叉反应性过敏原发生反应,该过敏原在9/14种CR物种中被检测到,包括德国小蠊、大蠊、蜚蠊、淡赤褐蠊和拟褐蠊属,浓度为100至10000 U/ml。相比之下,单克隆抗体3G12、8F4和1D4是德国小蠊特异性的。由单克隆抗体8F4定义的过敏原通过单克隆抗体亲和色谱法和高效液相色谱法的尺寸排阻进行纯化。它是一种36 kd的热敏感蛋白,等电点为5.2至5.4。过敏原10A6通过等电聚焦和高效液相色谱法进行部分纯化。它是一种热稳定的酸性蛋白(等电点3.15)。根据它们与先前描述的CR过敏原特性的比较,由单克隆抗体10A6和8F4定义的过敏原分别被临时指定为德国小蠊过敏原I(Bla g I)和德国小蠊过敏原II(Bla g II)。对六种市售CR皮肤试验提取物的检测表明,Bla g I水平存在200倍差异(4.7至1085 U/ml),只有两种提取物含有可检测到的Bla g II(248和324 U/ml)。结果表明,单克隆抗体可用于鉴定和定义CR过敏原,并且将单克隆抗体用作过敏原分析和纯化第一步的策略可能非常有效,特别是对于特征不明确的过敏原提取物。

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