Strategies for enriching and characterizing proteins with inhibitory properties on the yeast surface.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Arlinda Rezhdo, Catherine T Lessard, Mariha Islam, James A Van Deventer
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引用次数: 0

Abstract

Display technologies are powerful tools for discovering binding proteins against a broad range of biological targets. However, it remains challenging to adapt display technologies for the discovery of proteins that inhibit the enzymatic activities of targets. Here, we investigate approaches for discovering and characterizing inhibitory antibodies in yeast display format using a well-defined series of constructs and the target matrix metalloproteinase-9. Three previously reported antibodies were used to create model libraries consisting of inhibitory, non-inhibitory, and non-binding constructs. Conditions that preferentially enrich for inhibitory clones were identified for both magnetic bead-based enrichments and fluorescence-activated cell sorting. Half maximal inhibitory concentration (IC50) was obtained through yeast titration assays. The IC50 of the inhibitory antibody obtained in yeast display format falls within the confidence interval of the IC50 value determined in soluble form. Overall, this study identifies strategies for the discovery and characterization of inhibitory clones directly in yeast display format.

富集和鉴定酵母表面具有抑制特性的蛋白质的策略。
显示技术是发现与多种生物靶标结合蛋白的强大工具。然而,如何利用展示技术发现抑制靶标酶活性的蛋白质仍是一项挑战。在这里,我们利用一系列定义明确的构建物和靶标基质金属蛋白酶-9,研究了在酵母展示格式中发现和鉴定抑制性抗体的方法。之前报道的三种抗体被用来创建由抑制性、非抑制性和非结合性构建物组成的模型库。通过磁珠富集和荧光激活细胞分选,确定了优先富集抑制性克隆的条件。半数最大抑制浓度(IC50)是通过酵母滴定试验获得的。以酵母展示形式获得的抑制性抗体的 IC50 值在以可溶性形式确定的 IC50 值的置信区间内。总之,这项研究确定了直接以酵母展示格式发现和鉴定抑制性克隆的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Protein Engineering Design & Selection
Protein Engineering Design & Selection 生物-生化与分子生物学
CiteScore
3.30
自引率
4.20%
发文量
14
审稿时长
6-12 weeks
期刊介绍: Protein Engineering, Design and Selection (PEDS) publishes high-quality research papers and review articles relevant to the engineering, design and selection of proteins for use in biotechnology and therapy, and for understanding the fundamental link between protein sequence, structure, dynamics, function, and evolution.
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