Andrew Sarah M, Titus Julie A, Zumstein Louis
Chester College, Chester, United Kingdom.
Curr Protoc Toxicol. 2002 Feb;Appendix 3:A.3H.1-5. doi: 10.1002/0471140856.txa03hs10.
Conventional dialysis separates small molecules from large molecules by allowing diffusion of only the small molecules through selectively permeable membranes. Dialysis is usually used to change the salt (small-molecule) composition of a macromolecule-containing solution. The solution to be dialyzed is placed in a sealed dialysis membrane and immersed in a selected buffer; small solute molecules then equilibrate between the sample and the dialysate. Concomitant with the movement of small solutes across the membrane, however, is the movement of solvent in the opposite direction. There are several simple and relatively inexpensive methods for concentrating protein solutions. Dialysis against Aquacide 11A (Calbiochem), which removes water through the dialysis tubing, may be used. After concentration, the solution must be redialyzed into the appropriate buffer. Another method is to use Immersible-CX Ultrafilters (Millipore) which, when connected to a vacuum, remove everything below their molecular weight cutoff (MWCO). Alternatively, centrifugal concentrators, which are operated with the aid of ordinary laboratory centrifuges may be used.
传统透析通过仅允许小分子通过选择性渗透膜扩散来分离小分子和大分子。透析通常用于改变含大分子溶液的盐(小分子)组成。待透析的溶液置于密封的透析膜中,并浸入选定的缓冲液中;然后小溶质分子在样品和透析液之间达到平衡。然而,与小溶质跨膜移动同时发生的是溶剂沿相反方向的移动。有几种简单且相对便宜的方法可用于浓缩蛋白质溶液。可使用对Aquacide 11A(Calbiochem公司)进行透析,它通过透析管除去水分。浓缩后,溶液必须重新透析到合适的缓冲液中。另一种方法是使用Immersible-CX超滤器(密理博公司),当连接到真空时,它会除去分子量截留值(MWCO)以下的所有物质。或者,也可以使用借助普通实验室离心机操作的离心浓缩器。