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质粒DNA从阴离子交换剂上的解吸:洗脱时的盐浓度与质粒大小和负载量无关。

Desorption of plasmid DNA from anion exchangers: Salt concentration at elution is independent of plasmid size and load.

作者信息

Beck Jürgen, Biechele Matthias, Repik Christoph, Gruber Petra, Furtmüller Paul G, Hahn Rainer

机构信息

Department of Biotechnology, Institute of Bioprocess Science and Engineering, University of Natural Resources and Life Sciences, Vienna, Austria.

Baxalta Innovations GmbH, A Part of Takeda Companies, Orth an der Donau, Austria.

出版信息

J Sep Sci. 2023 Apr;46(8):e2200943. doi: 10.1002/jssc.202200943. Epub 2023 Feb 27.

Abstract

Detailed studies on the sorption behavior of plasmids on anion exchangers are rare compared to proteins. In this study, we systematically compare the elution behavior of plasmid DNA on three common anion exchange resins using linear gradient and isocratic elution experiments. Two plasmids of different lengths, 8 and 20 kbp, were studied and their elution characteristics were compared to a green fluorescent protein. Using established methods for determining retention characteristics of biomolecules in ion exchange chromatography lead to remarkable results. In contrast to the green fluorescent protein, plasmid DNA consistently elutes at one characteristic salt concentration in linear gradient elution. This salt concentration was the same independent of plasmid size but differed slightly for different resins. The behavior is consistent also at preparative loadings of plasmid DNA. Thus, only a single linear gradient elution experiment is sufficient to design elution in a process scale capture step. At isocratic elution conditions, plasmid DNA elutes only above this characteristic concentration. Even at slightly lower concentrations most plasmids remain tightly bound. We hypothesize, that the desorption is accompanied by a conformational change leading to a reduced number of available negative charges for binding. This explanation is supported by structural analysis before and after elution.

摘要

与蛋白质相比,关于质粒在阴离子交换剂上吸附行为的详细研究很少。在本研究中,我们使用线性梯度和等度洗脱实验系统地比较了质粒DNA在三种常见阴离子交换树脂上的洗脱行为。研究了两种不同长度(8和20 kbp)的质粒,并将它们的洗脱特性与绿色荧光蛋白进行了比较。使用已建立的方法测定离子交换色谱中生物分子的保留特性,得出了显著的结果。与绿色荧光蛋白不同,质粒DNA在线性梯度洗脱中始终在一个特征盐浓度下洗脱。该盐浓度与质粒大小无关,但不同树脂略有差异。在质粒DNA的制备负载量下,该行为也是一致的。因此,仅一次线性梯度洗脱实验就足以设计工艺规模捕获步骤中的洗脱。在等度洗脱条件下,质粒DNA仅在该特征浓度以上洗脱。即使在略低的浓度下,大多数质粒仍紧密结合。我们推测,解吸伴随着构象变化,导致可用于结合的负电荷数量减少。洗脱前后的结构分析支持了这一解释。

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