生物技术通报

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抗体修饰 DNA 测序酶的开发及其运用

宋辉, 曹文刚, 肖晓文, 杜军   

  1. 1. 北京擎科生物科技股份有限公司研究院,北京 100000 ; 2. 湖北擎科生物科技有限公司研发部,鄂州 436000
  • 发布日期:2024-04-19
  • 通讯作者: 杜军,男,副教授,研究方向 :发酵与合成生物学 ;E-mail: dujun@tsingke.com.cn.
  • 作者简介:宋辉,男,博士研究生,研究方向 :蛋白结构与功能研究 ;E-mail: songhui@tsingke.com.cn.
  • 基金资助:
    鄂州市科学技术局 2022 年科技计划项目 - 重点研发专项

Development and Application of Antibody Modified DNA Sequencing Enzymes

SONG Hui, CAO Wen-gang, XIAO Xiao-wen, DU Jun   

  1. 1.Research Institute, Beijing Tsingke Biotech Co.,Ltd., Beijing 100000;  2.Research and Development Department, Hubei Tsingke Biotechnoloy Co.,Ltd., Ezhou 436000
  • Online:2024-04-19

摘要: 【目的】开发一种新型 DNA 测序酶,解决一代测序技术应对复杂 DNA 结构模板所面临的主要挑战,如测序信号中断或测序信号快速衰减。【方法】从 NCBI 数据库中挖掘到了 Taq DNA 聚合酶和单链结合蛋白 SSB 基因信息,利用遗传融合、定点突变及基因设计技术获得了一种新型的测序酶 Sso-Sequenase。利用亲和层析和离子交换层析,获得了纯化的测序酶。利用抗体修饰技术改良了 Sso-Sequenase 的性能,并且利用 STR 技术对其热启动性能进行了表征。选取多组不同类型的复杂模板,采用一代技术对比分析了 Sso-Sequenase 测序酶试剂盒和传统 BigDye 测序试剂盒的测序表现。【结果】Sso-Sequenase 在大肠杆菌中稳定表达,纯度达到 95% 以上,产量高达 10.5 mg/L。当温度低于 35℃时,Sso-Sequenase 表现出热启动活性。在复杂模板的一代测序反应中,如重复序列、高 GC 和发夹结构等样本,Sso-Sequenase 测序酶成功完成了所有样本的测序,序列的平均碱基质量 QV 大于 20。相比而言,BigDye 测序试剂盒在处理这些复杂样本时,多数样本测序信号出现了显著衰减或中断。【结论】开发了一种纯度好、产量高,兼具热启动活性的 DNA 测序酶 Sso-Sequenase 及测序试剂盒,显著提高了复杂 DNA 结构模板(重复序列、高 GC 和发夹结构)测序成功率。

关键词: DNA 测序酶 , 抗体修饰 , 复杂模板 , 测序

Abstract: 【Objective】To develop a novel DNA sequencing enzyme that addresses the main challenges faced by first-generation sequencing technology when dealing with complex DNA structure templates, such as interruption of sequencing signals or rapid signal decay.【Method】Taq DNA polymerase and single-strand binding protein SSB gene sequences were mined from the NCBI database, and a novel sequencing enzyme, Sso-Sequenase, was obtained using genetic fusion, site-directed mutagenesis, and gene design techniques. The purified sequencing enzyme was obtained through affinity chromatography and ion exchange chromatography. The performance of Sso-Sequenase was improved using antibody modification technology, and its hot start performance was characterized using STR technology. A variety of complex templates were selected, and the sequencing performance of the Sso-Sequenase sequencing enzyme kit was compared with the traditional BigDye sequencing kit using Sanger sequencing.【Result】Sso-Sequenase was stably expressed in Escherichia coli, with a purity of over 95% and a yield of up to 10.5 mg/L. When the temperature was below 35℃ , Sso-Sequenase demonstrated hot start activity. In first-generation sequencing reactions with complex templates, such as those with repetitive sequences, high GC content, and hairpin structures, Sso-Sequenase successfully completed sequencing for all samples, with an average base quality value QV > 20. In contrast, the BigDye sequencing kit experienced significant signal decay or interruption when processing these complex samples.【Conclusion】A DNA sequencing enzyme, Sso-Sequenase, has been developed to possess exceptional purity, remarkable yield, and hot-start activity. These advancements have significantly bolstered the sequencing success rate for intricate DNA templates, including those characterized by repetitive sequences, high GC content, and hairpin structures.

Key words: DNA sequencing enzyme, antibody modification, complex templates, first-generation sequencing