Department of Biotechnology, University of Rijeka, Radmile Matejčić 2, 51000 Rijeka, Croatia.
Faculty of Engineering, University of Rijeka, Vukovarska 58, 51000 Rijeka, Croatia.
Molecules. 2020 Jul 22;25(15):3316. doi: 10.3390/molecules25153316.
One-bead-one-compound peptide libraries, developed following the top-down experimental approach, have attracted great interest in the identification of potential ligands or active peptides. By exploiting a reverse experimental design approach based on the bottom-up strategy, we aimed to develop simplified, maximally diverse peptide libraries that resulted in the successful characterization of mixture components. We show that libraries of 32 and 48 components can be successfully detected in a single run using chromatography coupled to mass spectrometry (UPLC-MS). The proposed libraries were further theoretically evaluated in terms of their composition and physico-chemical properties. By combining the knowledge obtained on single libraries we can cover larger sequence spaces and provide a controlled exploration of the peptide chemical space both theoretically and experimentally. Designing libraries by using the bottom-up approach opens up the possibility of rationally fine-tuning the library complexity based on the available analytical methods.
一单珠一化合物肽库是在自上而下的实验方法的基础上开发的,它在潜在配体或活性肽的鉴定方面引起了极大的兴趣。通过利用基于自下而上策略的反向实验设计方法,我们旨在开发简化的、最大限度多样化的肽库,从而成功地对混合物成分进行了特征描述。我们表明,使用与质谱联用的色谱法(UPLC-MS)可以在单次运行中成功检测到 32 和 48 个成分的文库。所提出的文库还可以从组成和物理化学性质方面进行理论评估。通过结合对单个文库获得的知识,我们可以覆盖更大的序列空间,并在理论和实验上对肽化学空间进行受控探索。通过自下而上的方法设计文库,为根据可用的分析方法合理调整文库的复杂性提供了可能性。