Protein renaturation by the liquid organic salt ethylammonium nitrate

被引:230
作者
Summers, CA [1 ]
Flowers, RA [1 ]
机构
[1] Univ Toledo, Dept Chem, Toledo, OH 43606 USA
关键词
hen egg white lysozyme; ethylammonium nitrate; differential scanning calorimetry;
D O I
10.1110/ps.9.10.2001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The room-temperature liquid salt, ethylammonium nitrate (EAN), has been used to enhance the recovery of denatured-reduced hen egg white lysozyme (HEWL). Our results show that EAN has the ability to prevent aggregation of the denatured protein. The use of EAN as a refolding additive is advantageous because the renaturation is a one-step process. When HEWL was denatured reduced using routine procedures and renatured using EAN as an additive, HEWL was found to regain 75% of its activity. When HEWL was denatured and reduced in near EAN, dilution resulted in over 90% recovery of active protein. An important aspect of this: process is that renaturation of HEWL occurs at concentrations of 1.6 mg/mL, whereas other renaturation processes occur at significantly lower protein concentrations. Additionally, the refolded-active protein can be separated from the molten salt by simple desalting methods. Although the use of a low-temperature molten salt in protein renaturation is unconventional, the power of this approach lies in its simplicity and utility.
引用
收藏
页码:2001 / 2008
页数:8
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