Cell-Free Systems and Their Importance in the Study of Membrane Proteins.

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Membrane Biology Pub Date : 2025-02-01 Epub Date: 2025-01-06 DOI:10.1007/s00232-024-00333-0
Karen Stephania González-Ponce, Samuel Celaya-Herrera, María Fernanda Mendoza-Acosta, Luz Edith Casados-Vázquez
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引用次数: 0

Abstract

The Cell-Free Protein Synthesis (CFPS) is an innovative technique used to produce various proteins. It has several advantages, including short expression times, no strain engineering is required, and toxic proteins such as membrane proteins can be produced. However, the most important advantage is that it eliminates the need for a living cell as a production system. Membrane proteins (MPs) are difficult to express in heterologous strains such as Escherichia coli. Modified strains must be used, and sometimes the strain produces them as inclusion bodies, which makes purification difficult. CFPS can avoid the problem of toxicity and, with the use of additives, allows the production of folded and functional membrane proteins. In this review, we focus on describing what cell-free systems are. We address the advantages and disadvantages of the different organisms that can be used to obtain cell extracts, including PURE systems, where the components are obtained recombinantly, and the methodologies that allow the synthesis of membrane proteins in cell-free systems, which, given their hydrophobic nature, require additives for their correct folding.

无细胞系统及其在膜蛋白研究中的重要性。
无细胞蛋白质合成(CFPS)是一种用于生产各种蛋白质的创新技术。它有几个优点,包括表达时间短,不需要菌株工程,可以产生有毒蛋白,如膜蛋白。然而,最重要的优点是它不需要活细胞作为生产系统。膜蛋白(MPs)在大肠杆菌等异源菌株中难以表达。必须使用修饰菌株,有时菌株产生它们作为包涵体,这使纯化变得困难。CFPS可以避免毒性问题,并且通过使用添加剂,可以生产折叠和功能性膜蛋白。在这篇综述中,我们着重于描述什么是无细胞系统。我们讨论了可用于获得细胞提取物的不同生物的优点和缺点,包括以重组方式获得组分的PURE系统,以及允许在无细胞系统中合成膜蛋白的方法,由于其疏水性,需要添加剂才能正确折叠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Membrane Biology
Journal of Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
4.20%
发文量
63
审稿时长
6-12 weeks
期刊介绍: The Journal of Membrane Biology is dedicated to publishing high-quality science related to membrane biology, biochemistry and biophysics. In particular, we welcome work that uses modern experimental or computational methods including but not limited to those with microscopy, diffraction, NMR, computer simulations, or biochemistry aimed at membrane associated or membrane embedded proteins or model membrane systems. These methods might be applied to study topics like membrane protein structure and function, membrane mediated or controlled signaling mechanisms, cell-cell communication via gap junctions, the behavior of proteins and lipids based on monolayer or bilayer systems, or genetic and regulatory mechanisms controlling membrane function. Research articles, short communications and reviews are all welcome. We also encourage authors to consider publishing ''negative'' results where experiments or simulations were well performed, but resulted in unusual or unexpected outcomes without obvious explanations. While we welcome connections to clinical studies, submissions that are primarily clinical in nature or that fail to make connections to the basic science issues of membrane structure, chemistry and function, are not appropriate for the journal. In a similar way, studies that are primarily descriptive and narratives of assays in a clinical or population study are best published in other journals. If you are not certain, it is entirely appropriate to write to us to inquire if your study is a good fit for the journal.
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