Fricke B
Department of Medicine, Martin Luther University, Halle, Germany.
Anal Biochem. 1993 Jul;212(1):154-9. doi: 10.1006/abio.1993.1306.
By adding salts (sodium chloride, ammonium sulfate), it is possible to induce phase separation in membrane-protein solubilisates containing Triton X-100 or Nonidet P-40 at temperatures between 0 and 20 degrees C. Other nonionic detergents of the Brij, Lubrol, and Tween series can also be used for this procedure. The salt concentration required for induction of phase separation is dependent on the hydrophobicity of the detergent used. For detergents of the Triton series it seems that detergents with lower hydrophilic lipophilic balance numbers need lower salt concentrations to separate the phases than those with larger hydrophilic parts. Ammonium sulfate precipitation as an initial purification step for membrane proteins should be avoided in the presence of the nonionic detergents tested. Instead of this procedure, phase separation induced by sodium chloride or ammonium sulfate can be recommended, as was proved for membrane-bound proteases of Pseudomonas aeruginosa and Bacillus cereus and for bacteriorhodopsin.
通过添加盐(氯化钠、硫酸铵),可以在0至20摄氏度的温度下,在含有Triton X-100或Nonidet P-40的膜蛋白增溶物中诱导相分离。Brij、Lubrol和Tween系列的其他非离子洗涤剂也可用于此过程。诱导相分离所需的盐浓度取决于所用洗涤剂的疏水性。对于Triton系列的洗涤剂,似乎亲水亲油平衡值较低的洗涤剂比具有较大亲水部分的洗涤剂需要更低的盐浓度来分离各相。在所测试的非离子洗涤剂存在的情况下,应避免将硫酸铵沉淀作为膜蛋白的初始纯化步骤。可以推荐用氯化钠或硫酸铵诱导相分离来替代此过程,这已在铜绿假单胞菌和蜡样芽孢杆菌的膜结合蛋白酶以及细菌视紫红质中得到证实。