Department of Biochemistry, Shimane University School of Medicine, Izumo 693-8501, Japan.
Department of Oral and Maxillofacial Surgery Shimane University School of Medicine, Izumo 693-8501, Japan.
Sci Rep. 2017 Mar 7;7:43480. doi: 10.1038/srep43480.
The recognition specificity of monoclonal antibodies (mAbs) has made mAbs among the most frequently used tools in both basic science research and in clinical diagnosis and therapies. Precise determination of the epitope allows the development of epitope tag systems to be used with recombinant proteins for various purposes. Here we describe a new family of tag derived from the epitope recognized by a highly specific mAb G196. The minimal epitope was identified as the five amino acid sequence Asp-Leu-Val-Pro-Arg. Permutation analysis was used to characterize the binding requirements of mAb G196, and the variable regions of the mAb G196 were identified and structurally analyzed by X-ray crystallography. Isothermal titration calorimetry revealed the high affinity (K = 1.25 nM) of the mAb G196/G196-epitope peptide interaction, and G196-tag was used to detect several recombinant cytosolic and nuclear proteins in human and yeast cells. mAb G196 is valuable for developing a new peptide tagging system for cell biology and biochemistry research.
单克隆抗体 (mAbs) 的识别特异性使其成为基础科学研究以及临床诊断和治疗中最常用的工具之一。精确确定抗原表位可用于开发用于各种目的的重组蛋白的抗原标签系统。在这里,我们描述了一种来自高度特异性 mAb G196 识别的抗原表位的新型标签家族。最小抗原表位被鉴定为五个氨基酸序列 Asp-Leu-Val-Pro-Arg。通过置换分析来表征 mAb G196 的结合要求,并通过 X 射线晶体学鉴定 mAb G196 的可变区并进行结构分析。等温滴定量热法揭示了 mAb G196/G196-抗原肽相互作用的高亲和力 (K = 1.25 nM),并用 G196 标签在人和酵母细胞中检测了几种重组胞质和核蛋白。mAb G196 可用于开发用于细胞生物学和生物化学研究的新型肽标记系统。