Salting out of Proteins Using Ammonium Sulfate Precipitation

被引:202
|
作者
Duong-Ly, Krisna C. [1 ]
Gabelli, Sandra B. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
关键词
D O I
10.1016/B978-0-12-420119-4.00007-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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' (Fig. 7.1). 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.
引用
收藏
页码:85 / 94
页数:10
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