创建首个识别hABCC6细胞外表位的单克隆抗体。

IF 3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
FEBS Letters Pub Date : 2021-03-01 Epub Date: 2020-11-28 DOI:10.1002/1873-3468.13991
Eszter Kozák, Bence Szikora, Attila Iliás, Péter K Jani, Zoltán Hegyi, Zsolt Matula, Dóra Dedinszki, Natália Tőkési, Krisztina Fülöp, Viola Pomozi, György Várady, Éva Bakos, Gabor E Tusnády, Imre Kacskovics, Andras Váradi
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引用次数: 2

摘要

ABCC6基因突变导致钙化疾病,如弹性假黄色瘤或婴儿期全身性动脉钙化。识别ABCC6细胞外表位(EC)的抗体的产生受到该蛋白的短EC片段的阻碍。为了克服这一限制,我们用表达人ABCC6 (hABCC6)的人胚胎肾293细胞免疫牛FcRn转基因小鼠,显示出增强的体液免疫反应。我们获得了一种识别hABCC6 EC表位的单克隆抗体,我们将其命名为mEChC6。有限的蛋白水解表明,该表位位于ABCC6 n端一半的一个环内,可能跨越338-347个氨基酸。mEChC6在hABCC6转基因小鼠的肝脏中识别hABCC6,验证了其特异性和EC与完整肝细胞的结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Creation of the first monoclonal antibody recognizing an extracellular epitope of hABCC6.

Mutations in the ABCC6 gene result in calcification diseases such as pseudoxanthoma elasticum or Generalized Arterial Calcification of Infancy. Generation of antibodies recognizing an extracellular (EC) epitope of ABCC6 has been hampered by the short EC segments of the protein. To overcome this limitation, we immunized bovine FcRn transgenic mice exhibiting an augmented humoral immune response with Human Embryonic Kidney 293 cells cells expressing human ABCC6 (hABCC6). We obtained a monoclonal antibody recognizing an EC epitope of hABCC6 that we named mEChC6. Limited proteolysis revealed that the epitope is within a loop in the N-terminal half of ABCC6 and probably spans amino acids 338-347. mEChC6 recognizes hABCC6 in the liver of hABCC6 transgenic mice, verifying both specificity and EC binding to intact hepatocytes.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
6.60
自引率
2.90%
发文量
303
审稿时长
1 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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