一种新型单克隆抗体对人小转甲状腺素聚集体的选择性识别。

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
A C Teixeira, Maria J Saraiva
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引用次数: 1

摘要

转甲状腺素变异体TTR Y78F的生化特征表明,该变异体与正常TTR一样采用四聚体构象,但在纤维形成途径中表现出中间结构的一些特征。据推测,原生Y78F可能代表TTR淀粉样变发生的早期事件。我们用重组变体TTR Y78F免疫TTR敲除小鼠。一个名为CE11的稳定杂交瘤,IgM同型,测试了几种可溶性重组TTR变异体的反应性,包括淀粉样变性和非淀粉样变性。CE11仅识别高淀粉样变TTR变体L55P、S52P、A97S、Y78F或酸化TTR wt制剂。同时,该克隆对可溶性野生型蛋白TTR V30M和TTR T119M均呈阴性。反应性随着低聚物的形成而增加,随着成熟原纤维的生长而降低。经过大小排斥层析(SEC)、夹夹式ELISA和天然免疫印迹,mAb识别出两个峰(峰1存在于物质在146 KDa以上的酸化和可溶性变异蛋白制剂中;峰2只存在于物质在66 - 146 KDa之间的可溶性L55P和S52P TTR制剂中。mAb CE11可能是研究抗TTR聚集治疗药物的潜在工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective recognition of human small transthyretin aggregates by a novel monoclonal antibody.

Biochemical characterisation of transthyretin variant TTR Y78F showed that this variant adopts a tetrameric conformation as normal TTR but exhibits some of the characteristics of an intermediate structure in the fibrillogenesis pathway. It was hypothesised that native Y78F might represent an early event in TTR amyloidogenesis. We immunised TTR knock out mice with recombinant variant TTR Y78F. One stable hybridoma named CE11, of the IgM isotype, was tested for reactivity towards several soluble recombinant TTR variants both amyloidogenic and non-amyloidogenic. CE11 only recognises the highly amyloidogenic TTR variants L55P, S52P, A97S, Y78F or acidified TTR wt preparations. At the same time, this clone was negative for TTR V30M, soluble wild type protein or TTR T119M. The reactivity increased with oligomer formation and decreased as mature fibrils grow. After size exclusion chromatography (SEC) followed by sandwich ELISA and native immunoblotting, the mAb recognised two peaks (i) peak 1 present in acidified and in soluble variant proteins preparations with material above 146 KDa (ii) peak 2 only present in soluble L55P and S52P TTR preparations with material between 66 and 146 KDa. mAb CE11 may be a potential tool to survey therapeutical agents against TTR aggregation.

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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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