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富集和鉴定具有抑制酵母表面特性的蛋白质的策略。

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

机构信息

Chemical and Biological Engineering Department, Tufts University, Medford, MA 02155, USA.

Biomedical Engineering Department, Tufts University, Medford, MA 02155, USA.

出版信息

Protein Eng Des Sel. 2023 Jan 21;36. doi: 10.1093/protein/gzac017.

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.

摘要

展示技术是发现针对广泛生物靶标的结合蛋白的有力工具。然而,将展示技术用于发现抑制靶标酶活性的蛋白质仍然具有挑战性。在这里,我们使用一系列定义良好的构建体和基质金属蛋白酶-9 靶标来研究在酵母展示形式中发现和表征抑制性抗体的方法。使用三种先前报道的抗体来创建由抑制性、非抑制性和非结合性构建体组成的模型文库。确定了用于磁珠富集和荧光激活细胞分选的优先富集抑制性克隆的条件。通过酵母滴定实验获得半数最大抑制浓度 (IC50)。在酵母展示形式中获得的抑制性抗体的 IC50 值在可溶性形式中确定的 IC50 值的置信区间内。总的来说,这项研究确定了在酵母展示形式中直接发现和表征抑制性克隆的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07df/10365883/5faa614864ea/gzac017ga1.jpg

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