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本文引用的文献

1
From systems to structure: bridging networks and mechanism.从系统到结构:连接网络和机制。
Mol Cell. 2013 Jan 24;49(2):222-31. doi: 10.1016/j.molcel.2013.01.003.
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The architecture of human general transcription factor TFIID core complex.人类通用转录因子 TFIID 核心复合物的结构。
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3
Comparative analysis of virus-host interactomes with a mammalian high-throughput protein complementation assay based on Gaussia princeps luciferase.基于海肾荧光素酶的哺乳动物高通量蛋白互补测定法对病毒-宿主相互作用组进行比较分析。
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IgG-Fc glycoengineering in non-mammalian expression hosts.非哺乳动物表达宿主中的 IgG-Fc 糖基工程。
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Correction: BTI-Tnao38, a new cell line derived from Trichoplusia ni, is permissive for AcMNPV infection and produces high levels of recombinant proteins.更正:BTI-Tnao38是一种源自粉纹夜蛾的新细胞系,对苜蓿银纹夜蛾核型多角体病毒(AcMNPV)感染敏感,并能产生高水平的重组蛋白。
BMC Biotechnol. 2012 Apr 24;12:12. doi: 10.1186/1472-6750-12-12.
6
SweetBac: a new approach for the production of mammalianised glycoproteins in insect cells.甜杆菌:昆虫细胞中生产哺乳动物糖蛋白的新方法。
PLoS One. 2012;7(4):e34226. doi: 10.1371/journal.pone.0034226. Epub 2012 Apr 2.
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An engineered eukaryotic protein glycosylation pathway in Escherichia coli.大肠杆菌中的工程化真核蛋白糖基化途径。
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Homology models guide discovery of diverse enzyme specificities among dipeptide epimerases in the enolase superfamily.同源模型指导在烯醇化酶超家族中的二肽差向异构酶中发现不同的酶特异性。
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The use of filler DNA for improved transfection and reduced DNA needs in transient gene expression with CHO and HEK cells.在CHO和HEK细胞的瞬时基因表达中使用填充DNA以改善转染并减少DNA用量。
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Transient transfection of insect Sf-9 cells in TubeSpin(®) bioreactor 50 tubes.在TubeSpin(®) 50管生物反应器中对昆虫Sf-9细胞进行瞬时转染。
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从结构基因组学角度看蛋白质生产:成就与未来需求

Protein production from the structural genomics perspective: achievements and future needs.

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, United States.

出版信息

Curr Opin Struct Biol. 2013 Jun;23(3):335-44. doi: 10.1016/j.sbi.2013.02.014. Epub 2013 May 1.

DOI:10.1016/j.sbi.2013.02.014
PMID:23642905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4163025/
Abstract

Despite a multitude of recent technical breakthroughs speeding high-resolution structural analysis of biological macromolecules, production of sufficient quantities of well-behaved, active protein continues to represent the rate-limiting step in many structure determination efforts. These challenges are only amplified when considered in the context of ongoing structural genomics efforts, which are now contending with multi-domain eukaryotic proteins, secreted proteins, and ever-larger macromolecular assemblies. Exciting new developments in eukaryotic expression platforms, including insect and mammalian-based systems, promise enhanced opportunities for structural approaches to some of the most important biological problems. Development and implementation of automated eukaryotic expression techniques promises to significantly improve production of materials for structural, functional, and biomedical research applications.

摘要

尽管最近有许多技术突破可以加速生物大分子的高分辨率结构分析,但大量生产行为良好、活性蛋白仍然是许多结构测定工作的限速步骤。当考虑到正在进行的结构基因组学工作时,这些挑战只会放大,这些工作现在正在应对多域真核蛋白、分泌蛋白和越来越大的大分子组装体。真核表达平台的令人兴奋的新发展,包括昆虫和哺乳动物系统,为解决一些最重要的生物学问题提供了更多的结构方法的机会。自动化真核表达技术的开发和实施有望显著提高结构、功能和生物医学研究应用材料的生产。