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使用AKTAxpress生产毫克级无标签重组人亲环素A(hCypA)和无标签人增殖细胞核抗原(hPCNA)的简化自动化方案。

Streamlined, automated protocols for the production of milligram quantities of untagged recombinant human cyclophilin-A (hCypA) and untagged human proliferating cell nuclear antigen (hPCNA) using AKTAxpress.

作者信息

Ludwig Cornelia, Wear Martin A, Walkinshaw Malcolm D

机构信息

The Edinburgh Protein Production Facility, Centre for Translational and Chemical Biology, University of Edinburgh, Michael Swann Building, Edinburgh EH9 3JR, UK.

出版信息

Protein Expr Purif. 2010 May;71(1):54-61. doi: 10.1016/j.pep.2009.12.001. Epub 2009 Dec 6.

Abstract

We developed streamlined, automated purification protocols for the production of milligram quantities of untagged recombinant human cyclophilin-A (hCypA) and untagged human proliferating cell nuclear antigen (hPCNA) from Escherichia coli, using the AKTAxpress chromatography system. The automated 2-step (cation exchange and size exclusion) purification protocol for untagged hCypA results in final purity and yields of 93% and approximately 5 mg L(-1) of original cell culture, respectively, in under 12h, including all primary sample processing and column equilibration steps. The novel automated 4-step (anion exchange, desalt, heparin-affinity and size exclusion, in linear sequence) purification protocol for untagged hPCNA results in final purity and yields of 87% and approximately 4 mg L(-1) of original cell culture, respectively, in under 24h, including all primary sample processing and column equilibration steps. This saves in excess of four full working days when compared to the traditional protocol, producing protein with similar final yield, purity and activity. Furthermore, it limits a time-dependent protein aggregation, a problem with the traditional protocol that results in a loss of final yield. Both automated protocols were developed to use generic commercially available pre-packed columns and automatically prepared minimal buffers, designed to eliminate user and system variations, maximize run reproducibility, standardize yield and purity between batches, increase throughput and reduce user input to a minimum. Both protocols represent robust generic methods for the automated production of untagged hCypA and hPCNA.

摘要

我们开发了简化的自动化纯化方案,使用AKTAxpress色谱系统从大肠杆菌中生产毫克量的无标签重组人亲环蛋白A(hCypA)和无标签人增殖细胞核抗原(hPCNA)。无标签hCypA的自动化两步(阳离子交换和尺寸排阻)纯化方案,在不到12小时内,最终纯度和产量分别达到93%和约5 mg L(-1)的原始细胞培养物,包括所有初级样品处理和柱平衡步骤。无标签hPCNA的新型自动化四步(阴离子交换、脱盐、肝素亲和和尺寸排阻,按线性顺序)纯化方案,在不到24小时内,最终纯度和产量分别达到87%和约4 mg L(-1)的原始细胞培养物,包括所有初级样品处理和柱平衡步骤。与传统方案相比,这节省了超过四个完整工作日的时间,生产出的蛋白质具有相似的最终产量、纯度和活性。此外,它还限制了时间依赖性蛋白质聚集,这是传统方案中导致最终产量损失的一个问题。这两种自动化方案都采用了通用的商业预装柱和自动制备的最小缓冲液,旨在消除用户和系统差异,最大限度地提高运行重现性,使批次间的产量和纯度标准化,提高通量并将用户输入降至最低。这两种方案都是用于无标签hCypA和hPCNA自动化生产的强大通用方法。

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