Biomarker Discovery by ORFeome Phage Display

噬菌体展示 噬菌体 平移(音频) 计算生物学 开放式参考框架 生物 基因组 肽库 噬菌体 互补DNA 基因组 打开阅读框 遗传学 基因 肽序列 抗体 大肠杆菌 古生物学 缩放 镜头(地质)
作者
Philip Alexander Heine,Rico Ballmann,Praveen Thevarajah,Giulio Russo,Gustavo Marçal Schmidt Garcia Moreira,Michael Hust
出处
期刊:Methods in molecular biology [Springer Science+Business Media]
卷期号:: 543-561 被引量:1
标识
DOI:10.1007/978-1-0716-3381-6_27
摘要

Phage display is an efficient and robust method for protein-protein interaction studies. Although it is mostly used for antibody generation, it can be also utilized for the discovery of immunogenic proteins that could be used as biomarkers. Through this technique, a genome or metagenome is fragmented and cloned into a phagemid vector. The resulting protein fragments from this genetic material are displayed on M13 phage surface, while the corresponding gene fragments are packaged. This packaging process uses the pIII deficient helperphage, called Hyperphage (M13KO7 ΔpIII), so open reading frames (ORFs) are enriched in these libraries, giving the name to this method: ORFeome phage display. After conducting a selection procedure, called "bio-panning," relevant immunogenic peptides or protein fragments are selected using purified antibodies or serum samples, and can be used as potential biomarkers. As ORFeome phage display is an in vitro method, only the DNA or cDNA of the species of interest is needed. Therefore, this approach is also suitable for organisms that are hard to cultivate, or metagenomic samples, for example. An additional advantage is that the biomarker discovery is not limited to surface proteins due to the presentation of virtually every kind of peptide or protein fragment encoded by the ORFeome on the phage surface. At last, the selected biomarkers can be the start for the development of diagnostic assays, vaccines, or protein interaction studies.
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