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首页> 外文期刊>Separation and Purification Technology >Non-affinity purification of a nanobody by void-exclusion anion exchange chromatography and multimodal weak cation exchange chromatography
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Non-affinity purification of a nanobody by void-exclusion anion exchange chromatography and multimodal weak cation exchange chromatography

机译:空隙排除阴离子交换色谱和多峰弱阳离子交换色谱法的非亲和纯化纳米体

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摘要

Multimodal chromatography resins have been reported to be excellent alternatives to classical absorbents in the purification of antibodies. In this study, void-exclusion anion exchange chromatography (VEAX) and electropositive multimodal chromatography (Capto MMC) were integrated for tag-free nanobody (2D5) purification. VEAX was systematically characterized for its potential use in the initial 2D5 separation. VEAX achieved a 89.9% reduction in host cell proteins (HCPs), a 99.6% reduction in DNA, a 99.9% reduction in endotoxins, and a 100% reduction in aggregates from periplasmic proteins, with a 2D5 recovery of near 100% and a purity enhancement from 3.5% to 25.0%. Subsequently, Capto MMC chromatography was seamlessly incorporated with direct protein loading for further purification. The recovery of this step was 80.5%. The entire two-step purification platform yielded 2D5 with 16 ppm of HCPs, 127 ppb of DNA, 35 EU/mL of endotoxins, with a total protein recovery of 80.5%. The purity of 2D5 was 98.5%. Moreover, this method had no effect on the affinity of 2D5. Meanwhile, the established method was also used to purify a nanobody against PD-L1 (KPU) with 95.8% purity, > 99% recovery, 55 ppm of HCPs, 289 ppb of DNA and 128 EU/mL of endotoxins. For the first time, this study reports a simplified, seamless and non-affinity purification platform for the purification of a tag-free nanobody, which provides a competitive alternative for the conventional affinity chromatography antibody purification strategy.
机译:据报道,多峰色谱树脂是抗体纯化中经典吸收剂的优异替代品。在该研究中,将空隙排除阴离子交换色谱(VEAX)和正压多峰色谱(Capto MMC)整合用于无标签的纳米曲面(2D5)纯化。 VEAx系统地具有其在初始2D5分离中的潜在使用。 VeAx在宿主细胞蛋白(HCP)降低89.9%,DNA降低99.6%,内毒素的99.9%,来自周质蛋白的聚集体减少了100%,具有近100%的2D5恢复和纯度增强从3.5%到25.0%。随后,将CAPTOMMC色谱法无缝地掺入直接蛋白质负载以进行进一步纯化。恢复这一步骤为80.5%。整个两步净化平台产生2D5,具有16ppm的HCP,127ppb的DNA,35欧欧/毫升内毒素,总蛋白质回收率为80.5%。 2D5的纯度为98.5%。此外,该方法对2D5的亲和力没有影响。同时,已建立的方法还用于纯化纳米抗体,纯度纯度为95.8%纯度,> 99%回收率,55ppm的HCP,289ppb和128 eU / ml内毒素。本研究首次报告了一种简化的无缝和非亲和纯化平台,用于纯化可自由标记的纳米体,其为常规亲和层析抗体纯化策略提供了竞争的替代品。

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  • 作者单位

    Chinese Acad Sci Qingdao Inst Bioenergy &

    Bioproc Technol CAS Key Lab Biobased Mat Qingdao Shandong Peoples R China;

    Shenzhen Innova Nanobodi Co Ltd 7018 Caitian Rd Shenzhen 518000 Peoples R China;

    Chinese Acad Sci Qingdao Inst Bioenergy &

    Bioproc Technol CAS Key Lab Biobased Mat Qingdao Shandong Peoples R China;

    Shenzhen Innova Nanobodi Co Ltd 7018 Caitian Rd Shenzhen 518000 Peoples R China;

    Chinese Acad Sci Qingdao Inst Bioenergy &

    Bioproc Technol CAS Key Lab Biobased Mat Qingdao Shandong Peoples R China;

    Shenzhen Innova Nanobodi Co Ltd 7018 Caitian Rd Shenzhen 518000 Peoples R China;

    Inzhou Med Univ 346 Guanhai Rd Yantai 264003 Peoples R China;

    Chinese Acad Sci Qingdao Inst Bioenergy &

    Bioproc Technol CAS Key Lab Biobased Mat Qingdao Shandong Peoples R China;

    Chinese Acad Sci Qingdao Inst Bioenergy &

    Bioproc Technol CAS Key Lab Biobased Mat Qingdao Shandong Peoples R China;

    Chinese Acad Sci Qingdao Inst Bioenergy &

    Bioproc Technol CAS Key Lab Biobased Mat Qingdao Shandong Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分离过程;气化工艺;
  • 关键词

    Nanobody; Non-affinity; Purification; Void-exclusion anion exchange chromatography; Capto MMC;

    机译:Nanobody;非亲和力;纯化;空隙排除阴离子交换色谱;CAPTO MMC;

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