Development of a Novel Polyclonal Antibody-Based Immunoassay for the Quantitation of Non-Albumin Urinary Proteins

W. Haigh, D. Guralski, L. Arrigo, J. Letsinger, Michele V. Clarke, R. MacIsaac, G. Jerums, D. L. Very
{"title":"Development of a Novel Polyclonal Antibody-Based Immunoassay for the Quantitation of Non-Albumin Urinary Proteins","authors":"W. Haigh, D. Guralski, L. Arrigo, J. Letsinger, Michele V. Clarke, R. MacIsaac, G. Jerums, D. L. Very","doi":"10.2174/1874241601306010001","DOIUrl":null,"url":null,"abstract":"Background:\n Better diagnostic methods to detect urinary proteinuria or albuminuria, important indicators of\ndiabetic kidney disease, are needed. Here, we describe the development and performance qualification of a new immunoassay\nfor the quantitation of non-albumin urinary proteins of 20 to 90 kilodaltons.\n Methods:\n Urinary proteins, purified from pooled, 24-hour, diabetic urines, were immunoabsorbed to remove albumin,\nelectrophoretically characterized, and identified by mass spectrometry. Sheep anti-urinary protein polyclonal antibodies\nwere immunoabsorbed to remove albumin reactivity. Major immunoreactive specificities of the polyclonal antibody were\nidentified by Western blot. A polyclonal antibody-based competitive immunoassay was developed and performanceevaluated.\nAn unpaired t-test (α = 0.05) and a receiver-operating characteristic curve were used to evaluate the measurement\nof 24-hour urinary protein excretion rates in distinguishing between normal, proteinuric, and albuminuric samples.\n Results:\n Approximately 380 mg of urinary protein was purified from 6.0 g of total urinary proteins. Mass spectrometry\nidentified more than 36 different proteins in the purified preparation. The anti-urinary protein polyclonal antibody possessed\nsignificant immunoreactivity towards transferrin, IgG chains, alpha-1-acid glycoprotein, zinc-alpha-2-glycoprotein,\nprostaglandin-H2-d-isomerase, and alpha-1-microglobulin. The competitive immunoassay exhibited excellent analytical\nand clinical performance. Measurement of urinary protein excretion rates could distinguish between normoproteinuric and\nproteinuric samples (p < 0.0001; area under the curve = 0.6900) and between normoalbuminuric and albuminuric samples\n(p < 0.0001; area under the curve = 0.8782).\n Conclusion:\n Measurement of urinary protein excretion rates using the urinary protein immunoassay is clinically equivalent\nto laboratory methods of quantitating total urinary protein or albumin in identifying proteinuria and albuminuria.","PeriodicalId":112973,"journal":{"name":"The Open Clinical Chemistry Journal","volume":"30 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Clinical Chemistry Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874241601306010001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Background: Better diagnostic methods to detect urinary proteinuria or albuminuria, important indicators of diabetic kidney disease, are needed. Here, we describe the development and performance qualification of a new immunoassay for the quantitation of non-albumin urinary proteins of 20 to 90 kilodaltons. Methods: Urinary proteins, purified from pooled, 24-hour, diabetic urines, were immunoabsorbed to remove albumin, electrophoretically characterized, and identified by mass spectrometry. Sheep anti-urinary protein polyclonal antibodies were immunoabsorbed to remove albumin reactivity. Major immunoreactive specificities of the polyclonal antibody were identified by Western blot. A polyclonal antibody-based competitive immunoassay was developed and performanceevaluated. An unpaired t-test (α = 0.05) and a receiver-operating characteristic curve were used to evaluate the measurement of 24-hour urinary protein excretion rates in distinguishing between normal, proteinuric, and albuminuric samples. Results: Approximately 380 mg of urinary protein was purified from 6.0 g of total urinary proteins. Mass spectrometry identified more than 36 different proteins in the purified preparation. The anti-urinary protein polyclonal antibody possessed significant immunoreactivity towards transferrin, IgG chains, alpha-1-acid glycoprotein, zinc-alpha-2-glycoprotein, prostaglandin-H2-d-isomerase, and alpha-1-microglobulin. The competitive immunoassay exhibited excellent analytical and clinical performance. Measurement of urinary protein excretion rates could distinguish between normoproteinuric and proteinuric samples (p < 0.0001; area under the curve = 0.6900) and between normoalbuminuric and albuminuric samples (p < 0.0001; area under the curve = 0.8782). Conclusion: Measurement of urinary protein excretion rates using the urinary protein immunoassay is clinically equivalent to laboratory methods of quantitating total urinary protein or albumin in identifying proteinuria and albuminuria.
一种新的基于多克隆抗体的非白蛋白尿蛋白定量免疫测定方法的建立
背景:需要更好的诊断方法来检测尿蛋白尿或尿白蛋白尿,这是糖尿病肾病的重要指标。在这里,我们描述了一种新的免疫测定法的发展和性能鉴定,用于定量20至90千道尔顿的非白蛋白尿蛋白。方法:从24小时的糖尿病尿中纯化尿蛋白,免疫吸收去除白蛋白,电泳表征,质谱鉴定。羊抗尿蛋白多克隆抗体免疫吸附去除白蛋白反应性。Western blot鉴定了该多克隆抗体的主要免疫反应特异性。建立了一种基于多克隆抗体的竞争性免疫分析法,并对其性能进行了评价。采用非配对t检验(α = 0.05)和受体工作特征曲线来评价24小时尿蛋白排泄率在区分正常、蛋白尿和白蛋白尿样品中的测量值。结果:从6.0 g总尿蛋白中纯化出约380 mg尿蛋白。质谱分析在纯化的制剂中鉴定出超过36种不同的蛋白质。该抗尿蛋白多克隆抗体对转铁蛋白、IgG链、α -1-酸性糖蛋白、锌- α -2-糖蛋白、前列腺素- h2 -d异构酶和α -1-微球蛋白具有显著的免疫反应性。竞争性免疫分析法具有良好的分析和临床性能。尿蛋白排泄率的测定可以区分正常蛋白尿和蛋白尿样本(p < 0.0001;曲线下面积= 0.6900)和正常蛋白尿和蛋白尿样本之间(p < 0.0001;曲线下面积= 0.8782)。结论:用尿蛋白免疫分析法测定尿蛋白排泄率在临床上等同于实验室测定总尿蛋白或白蛋白的方法来鉴别蛋白尿和白蛋白尿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书