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用于基因表达和抗体筛选的蛋白质微阵列。

Protein microarrays for gene expression and antibody screening.

作者信息

Lueking A, Horn M, Eickhoff H, Büssow K, Lehrach H, Walter G

机构信息

Max Planck Institute for Molecular Genetics, Ihnestrasse 73, Berlin, D-14195, Germany.

出版信息

Anal Biochem. 1999 May 15;270(1):103-11. doi: 10.1006/abio.1999.4063.

Abstract

Proteins translate genomic sequence information into function, enabling biological processes. As a complementary approach to gene expression profiling on cDNA microarrays, we have developed a technique for high-throughput gene expression and antibody screening on chip-size protein microarrays. Using a picking/spotting robot equipped with a new transfer stamp, protein solutions were gridded onto polyvinylidene difluoride filters at high density. Specific purified protein was detected on the filters with high sensitivity (250 amol or 10 pg of a test protein). On a microarray made from bacterial lysates of 92 human cDNA clones expressed in a microtiter plate, putative protein expressors could be reliably identified. The rate of false-positive clones, expressing proteins in incorrect reading frames, was low. Product specificity of selected clones was confirmed on identical microarrays using monoclonal antibodies. Cross-reactivities of some antibodies with unrelated proteins imply the use of protein microarrays for antibody specificity screening against whole libraries of proteins. Because this application would not be restricted to antigen-antibody systems, protein microarrays should provide a general resource for high-throughput screens of gene expression and receptor-ligand interactions.

摘要

蛋白质将基因组序列信息转化为功能,从而实现生物过程。作为cDNA微阵列基因表达谱分析的一种补充方法,我们开发了一种在芯片大小的蛋白质微阵列上进行高通量基因表达和抗体筛选的技术。使用配备新转移印章的挑选/点样机器人,将蛋白质溶液高密度地网格状点样到聚偏二氟乙烯滤膜上。在滤膜上以高灵敏度(250 amol或10 pg的测试蛋白)检测到特定的纯化蛋白。在由在微量滴定板中表达的92个人类cDNA克隆的细菌裂解物制成的微阵列上,可以可靠地鉴定出推定的蛋白质表达体。在错误阅读框中表达蛋白质的假阳性克隆率很低。使用单克隆抗体在相同的微阵列上证实了所选克隆的产物特异性。一些抗体与无关蛋白质的交叉反应性意味着可使用蛋白质微阵列针对整个蛋白质文库进行抗体特异性筛选。由于这种应用不限于抗原-抗体系统,蛋白质微阵列应为基因表达和受体-配体相互作用的高通量筛选提供一种通用资源。

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