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By-passing selection: direct screening for antibody-antigen interactions using protein arrays.

机译:旁路选择:使用蛋白质阵列直接筛选抗体-抗原相互作用。

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摘要

We have developed a system to identify highly specific antibody-antigen interactions by protein array screening. This removes the need for selection using animal immunisation or in vitro techniques such as phage or ribosome display. We screened an array of 27 648 human foetal brain proteins with 12 well-expressed antibody fragments that had not previously been exposed to any antigen. Four highly specific antibody-antigen pairs were identified, including three antibodies that bind proteins of unknown function. The target proteins were expressed at a very low copy number on the array, emphasising the unbiased nature of the screen. The specificity and sensitivity of binding demonstrates that this 'naive' screening approach could be applied to the high throughput isolation of specific antibodies against many different targets in the human proteome.
机译:我们已经开发了一种通过蛋白质阵列筛选来鉴定高度特异性的抗体-抗原相互作用的系统。这样就无需使用动物免疫或体外技术(例如噬菌体或核糖体展示)进行选择。我们筛选了27 648个人类胎儿脑蛋白阵列,其中包含12个表达良好的抗体片段,这些片段以前从未暴露于任何抗原。鉴定出四个高度特异性的抗体-抗原对,包括三个结合未知功能蛋白的抗体。目标蛋白在阵列上以非常低的拷贝数表达,强调了屏幕的无偏性。结合的特异性和敏感性表明,这种“幼稚”的筛选方法可用于高通量分离针对人类蛋白质组中许多不同靶标的特异性抗体。

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