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功能性工程化通道与孔道(综述)

Functional engineered channels and pores (Review).

作者信息

Bayley Hagan, Jayasinghe Lakmal

机构信息

Department of Chemistry, University of Oxford, Oxford OX1 3TA, UK.

出版信息

Mol Membr Biol. 2004 Jul-Aug;21(4):209-20. doi: 10.1080/09687680410001716853.

Abstract

Significant progress has been made in membrane protein engineering over the last 5 years, based largely on the re-design of existing scaffolds. Engineering techniques that have been employed include direct genetic engineering, both covalent and non-covalent modification, unnatural amino acid mutagenesis and total synthesis aided by chemical ligation of unprotected fragments. Combinatorial mutagenesis and directed evolution remain, by contrast, underemployed. Techniques for assembling and purifying heteromeric multisubunit pores have been improved. Progress in the de novo design of channels and pores has been slower. But, we are at the beginning of a new era in membrane protein engineering based on the accelerating acquisition of structural information, a better understanding of molecular motion in membrane proteins, technical improvements in membrane protein refolding and the application of computational approaches developed for soluble proteins. In addition, the next 5 years should see further advances in the applications of engineered channels and pores, notably in therapeutics and sensor technology.

摘要

在过去5年里,膜蛋白工程取得了重大进展,这在很大程度上基于对现有支架的重新设计。所采用的工程技术包括直接基因工程、共价和非共价修饰、非天然氨基酸诱变以及通过未保护片段的化学连接辅助进行的全合成。相比之下,组合诱变和定向进化的应用仍然不足。组装和纯化异源多亚基孔的技术已经得到改进。通道和孔的从头设计进展较慢。但是,基于结构信息获取的加速、对膜蛋白分子运动的更好理解、膜蛋白重折叠的技术改进以及为可溶性蛋白开发的计算方法的应用,我们正处于膜蛋白工程的一个新时代的开端。此外,未来5年,工程化通道和孔的应用有望取得进一步进展,尤其是在治疗学和传感器技术方面。

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