Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, United States of America; Department of Chemistry, University of California, Davis, United States of America.
Department of Chemistry, University of California, Davis, United States of America; Department of Biomedical Engineering, University of California, Davis, United States of America.
Biochim Biophys Acta Biomembr. 2020 Oct 1;1862(10):183394. doi: 10.1016/j.bbamem.2020.183394. Epub 2020 Jun 18.
Membrane active peptides (MAPs) have gained wide interest due to their far reaching applications in drug discovery and drug delivery. The search for new MAPs, however, has been largely skewed with bias selecting for physicochemical parameters believed to be important for membrane activity, such as alpha helicity, cationicity and hydrophobicity. Here we carry out a search-and-find strategy to screen a 100,000-membered one-bead-one-compound (OBOC) combinatorial peptide library for lead compounds, agnostic of those physicochemical constraints. Such a synthetic strategy also permits expansion of our peptide repertoire to include unnatural amino acids. Using this approach, we discovered a structurally unique lead peptide LBF14, a linear 14-mer peptide, that induces gross morphological disruption of membranes, irrespective of membrane composition. Further, we demonstrate that the unique insertion mechanism of the peptide, visualized by spinning disc confocal microscopy and further analyzed by electron paramagnetic resonance measurements, may be the cause of this large scale membrane deformation. We also demonstrate the robustness, reproducibility, and potential application of this technique to discover and characterize new membrane active peptides that display activity by local insertion and subsequent allosteric effects leading to global membrane disruption.
由于其在药物发现和药物输送方面的广泛应用,膜活性肽 (MAPs) 引起了广泛的关注。然而,新的 MAPs 的研究主要偏向于选择那些被认为对膜活性很重要的理化参数,如α螺旋性、阳离子性和疏水性。在这里,我们采用搜索和发现策略,对一个 100,000 个成员的单珠一单化合物 (OBOC) 组合肽文库进行筛选,寻找先导化合物,而不考虑这些理化限制。这种合成策略还允许我们扩展肽库,包括非天然氨基酸。使用这种方法,我们发现了一种结构独特的先导肽 LBF14,一种线性 14 肽,它可以引起膜的明显形态破坏,而与膜组成无关。此外,我们通过旋转盘共聚焦显微镜观察并通过电子顺磁共振测量进一步分析,证明了该肽独特的插入机制可能是导致这种大规模膜变形的原因。我们还证明了这种技术的稳健性、可重复性和潜在应用,以发现和表征新的膜活性肽,这些肽通过局部插入和随后的变构效应导致全局膜破坏而显示活性。