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使用硫酸铵沉淀法对蛋白质进行盐析。

Salting out of proteins using ammonium sulfate precipitation.

作者信息

Duong-Ly Krisna C, Gabelli Sandra B

机构信息

Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Methods Enzymol. 2014;541:85-94. doi: 10.1016/B978-0-12-420119-4.00007-0.

Abstract

Protein solubility is affected by ions. At low ion concentrations (<0.5 M), protein solubility increases along with ionic strength. Ions in the solution shield protein molecules from the charge of other protein molecules in what is known as 'salting-in'. At a very high ionic strength, protein solubility decreases as ionic strength increases in the process known as 'salting-out'. Thus, salting out can be used to separate proteins based on their solubility in the presence of a high concentration of salt. In this protocol, ammonium sulfate will be added incrementally to an E. coli cell lysate to isolate a recombinantly over-expressed protein of 20 kDa containing no cysteine residues or tags.

摘要

蛋白质的溶解度受离子影响。在低离子浓度(<0.5 M)下,蛋白质溶解度随离子强度增加而升高。溶液中的离子通过所谓的“盐溶”作用,使蛋白质分子免受其他蛋白质分子电荷的影响。在非常高的离子强度下,蛋白质溶解度会随着离子强度增加而降低,此过程称为“盐析”。因此,盐析可用于基于蛋白质在高浓度盐存在下的溶解度来分离蛋白质。在本实验方案中,将逐步向大肠杆菌细胞裂解液中添加硫酸铵,以分离一种重组过表达的20 kDa蛋白质,该蛋白质不含半胱氨酸残基或标签。

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