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Complex Reconstitution and Characterization by Combining Co-expression Techniques in Escherichia coli with High-Throughput

机译:用高吞吐量将Co-Depication Techs与高吞吐量组合中的复合重构和特征

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Single protein expression technologies have strongly benefited from the Structural Genomics initiatives that have introduced parallelization at the laboratory level. Specifically, the developments made in the wake of these initiatives have revitalized the use of Escherichia coli as major host for heterologous protein expression. In parallel to these improvements for single expression, technologies for complex reconstitution by co-expression in E. coli have been developed. Assessments of these co-expression technologies have highlighted the need for combinatorial experiments requiring automated protocols. These requirements can be fulfilled by adapting the high-throughput approaches that have been developed for single expression to the co-expression technologies. Yet, challenges are laying ahead that further need to be addressed and that are only starting to be taken into account in the case of single expression. These notably include the biophysical characterization of the samples at the small-scale level. Specifically, these approaches aim at discriminating the samples at an early stage of their production based on various biophysical criteria leading to cost-effectiveness and time-saving. This chapter addresses these various issues to provide the reader with a broad and comprehensive overview of complex reconstitution and characterization by co-expression in E. coli.
机译:单一蛋白表达技术强烈受益于在实验室水平引入平行化的结构基因组学举措。具体而言,在这些举措之后制造的发展使得使用大肠杆菌作为异源蛋白表达的主要宿主的使用。与这些改进的单一表达的改进平行,已经开发了通过在大肠杆菌中共同表达复杂重构的技术。这些共表达技术的评估突出了需要自动协议的组合实验的需求。通过调整为单一表达式开发的高吞吐量方法,可以满足这些要求。然而,挑战正在展开,进一步需要解决,并且在单一表达式中才能开始考虑到。这些显着地包括在小规模水平下对样品的生物物理表征。具体而言,这些方法旨在基于导致成本效益和节省时间的各种生物物理标准在其生产早期歧视样本。本章解决了这些各种问题,为读者提供了广泛而全面的复杂重建和通过COLI中的共同表达表征的广泛概述。

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