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利用靶向展示磁化酵母筛选 mRNA 展示肽文库以鉴定配体。

Use of Target-Displaying Magnetized Yeast in Screening mRNA-Display Peptide Libraries to Identify Ligands.

机构信息

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.

出版信息

ACS Comb Sci. 2020 Dec 14;22(12):738-744. doi: 10.1021/acscombsci.0c00171. Epub 2020 Oct 22.

Abstract

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.

摘要

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。

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