The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
J Mol Biol. 2021 Jul 23;433(15):167071. doi: 10.1016/j.jmb.2021.167071. Epub 2021 May 28.
Antibodies provide a comprehensive record of the encounters with threats and insults to the immune system. The ability to examine the repertoire of antibodies in serum and discover those that best represent "discriminating features" characteristic of various clinical situations, is potentially very useful. Recently, phage display technologies combined with Next-Generation Sequencing (NGS) produced a powerful experimental methodology, coined "Deep-Panning", in which the spectrum of serum antibodies is probed. In order to extract meaningful biological insights from the tens of millions of affinity-selected peptides generated by Deep-Panning, advanced bioinformatics algorithms are a must. In this study, we describe Motifier, a computational pipeline comprised of a set of algorithms that systematically generates discriminatory peptide motifs based on the affinity-selected peptides identified by Deep-Panning. These motifs are shown to effectively characterize antibody binding activities and through the implementation of machine-learning protocols are shown to accurately classify complex antibody mixtures representing various biological conditions.
抗体为免疫系统遭遇的威胁和侵害提供了全面的记录。检查血清中抗体库并发现那些最能代表各种临床情况“鉴别特征”的能力具有很大的潜在用途。最近,噬菌体展示技术与下一代测序(NGS)相结合,产生了一种强大的实验方法,称为“Deep-Panning”,在此方法中可以探测血清抗体的范围。为了从 Deep-Panning 产生的数以千万计的亲和选择肽中提取有意义的生物学见解,必须使用先进的生物信息学算法。在这项研究中,我们描述了 Motifier,这是一个计算管道,包含一组算法,这些算法可以根据 Deep-Panning 鉴定的亲和选择肽系统地生成有区别的肽基序。这些基序被证明可以有效地描述抗体结合活性,并通过实施机器学习协议,准确地对代表各种生物学条件的复杂抗体混合物进行分类。