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创建首个识别 hABCC6 细胞外表位的单克隆抗体。

Creation of the first monoclonal antibody recognizing an extracellular epitope of hABCC6.

机构信息

Institute of Enzymology, Research Center for Natural Sciences, Hungarian Academy of Sciences Centre of Excellence, Budapest, Hungary.

Department of Immunology, Eötvös Loránd University of Budapest, Hungary.

出版信息

FEBS Lett. 2021 Mar;595(6):789-798. doi: 10.1002/1873-3468.13991. Epub 2020 Nov 28.

Abstract

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.

摘要

ABCC6 基因突变会导致钙化疾病,如假性黄色瘤弹性组织变性或婴儿全身性动脉钙化。由于 ABCC6 蛋白的胞外(EC)片段较短,生成识别其 EC 表位的抗体一直受到阻碍。为了克服这一限制,我们用表达人 ABCC6(hABCC6)的人胚肾 293 细胞免疫转染牛 FcRn 转基因小鼠,该细胞能增强体液免疫反应。我们获得了一种识别 hABCC6 的 EC 表位的单克隆抗体,我们将其命名为 mEChC6。有限蛋白酶解表明,该表位位于 ABCC6 氨基端一半的环内,可能跨越氨基酸 338-347。mEChC6 识别 hABCC6 转基因小鼠肝脏中的 hABCC6,这验证了其特异性和对完整肝细胞的 EC 结合。

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