Department of Chemical and Biomolecular Engineering, North Carolina State University, 911 Partners Way, Room 2-009, Raleigh, North Carolina 27606, United States.
Biomanufacturing Training and Education Center (BTEC), North Carolina State University, 850 Oval Drive, Raleigh, North Carolina 27606, United States.
ACS Comb Sci. 2020 Dec 14;22(12):738-744. doi: 10.1021/acscombsci.0c00171. Epub 2020 Oct 22.
This work presents the first use of yeast-displayed protein targets for screening mRNA-display libraries of cyclic and linear peptides. The WW domains of Yes-Associated Protein 1 (WW-YAP) and mitochondrial import receptor subunit TOM22 were adopted as protein targets. Yeast cells displaying WW-YAP or TOM22 were magnetized with iron oxide nanoparticles to enable the isolation of target-binding mRNA-peptide fusions. Equilibrium adsorption studies were conducted to estimate the binding affinity () of select WW-YAP-binding peptides: values of 37 and 4 μM were obtained for cyclo[M-AFRLC-K] and its linear cognate, and 40 and 3 μM for cyclo[M-LDFVNHRSRG-K] and its linear cognate, respectively. TOM22-binding peptide cyclo[M-PELNRAI-K] was conjugated to magnetic beads and incubated with yeast cells expressing TOM22 and luciferase. A luciferase-based assay showed a 4.5-fold higher binding of TOM22 yeast compared to control cells. This work demonstrates that integrating mRNA- and yeast-display accelerates the discovery of peptide ligands.
这项工作首次利用酵母展示的蛋白质靶标筛选环肽和线性肽的 mRNA 展示文库。采用 YAP 相关蛋白 1(WW-YAP)和线粒体导入受体亚基 TOM22 的 WW 结构域作为蛋白质靶标。用氧化铁纳米颗粒磁化表达 WW-YAP 或 TOM22 的酵母细胞,以分离靶标结合的 mRNA-肽融合物。进行平衡吸附研究以估计选定的 WW-YAP 结合肽的结合亲和力():对于环[M-AFRLC-K]及其线性同源物,分别获得了 37 和 4 μM 的值,对于环[M-LDFVNHRSRG-K]及其线性同源物,分别获得了 40 和 3 μM 的值。将 TOM22 结合肽环[M-PELNRAI-K]与磁珠偶联,并与表达 TOM22 和荧光素酶的酵母细胞孵育。基于荧光素酶的测定显示,与对照细胞相比,TOM22 酵母的结合提高了 4.5 倍。这项工作表明,整合 mRNA 和酵母展示可加速肽配体的发现。