Frenkel M J, Blagrove R J
J Chromatogr. 1975 Sep 3;111(2):397-402. doi: 10.1016/s0021-9673(00)99289-6.
The inclusion of urea has been found to eliminate adsorption of protein-sodium dodecyl sulphate (SDS) complexes to controlled pore glass. Using buffer containing 6 M urea, 0.5% SDS and glass with pore diameter 12.3 nm, it is possible to determine protein molecular weights in the range 3500-12,000. Results with glass of larger pore diameter (25.5 nm) are similar to those reported in the absence of urea in the molecular-weight range 12,000-140,000. Controlled pore glass chromatography also permits the study of the relative importance of conformation free of charge effects for those proteins which deviate from the normal calibration curve for SDS-polyacrylamide gels.
已发现加入尿素可消除蛋白质 - 十二烷基硫酸钠(SDS)复合物在可控孔径玻璃上的吸附。使用含有6M尿素、0.5% SDS的缓冲液以及孔径为12.3nm的玻璃,能够测定分子量在3500至12,000范围内的蛋白质分子量。对于孔径较大(25.5nm)的玻璃,在分子量范围12,000至140,000内得到的结果与未添加尿素时所报道的结果相似。可控孔径玻璃色谱法还允许对那些偏离SDS - 聚丙烯酰胺凝胶正常校准曲线的蛋白质,研究无电荷效应构象的相对重要性。