Hirabayashi J, Kasai K
Department of Biological Chemistry, Teikyo University, Sagamiko, Japan.
J Chromatogr A. 1996 Jan 26;722(1-2):135-42. doi: 10.1016/0021-9673(95)00505-6.
Improved resolution in slalom chromatography, a novel size-fractionation method discovered recently for relatively large DNA molecules (> 5 kpb), was obtained by using columns generally employed for reversed-phase chromatography: i.e., two types of Capcell-Pak (methyl or phenyl-derivatized 5-microns microbeads), and five types of Hypersil-3 packings (trimethylsilyl, dimethyloctyl, cyanopropyl, octadecyl or phenyl-derivatized 3-microns microbeads). The resolution of 5-15-kbp DNA was significantly improved by employing these columns, though the separation characteristics differed. When Capcell-Pak columns were used with a normal low-salt eluting solvent (10 mM sodium phosphate, pH 6.8, 1 mM EDTA), chromatograms were obtained for lambda/HindIII fragments (a mixture of 0.1, 0.5, 2.0, 2.3, 4.4, 6.6, 9.4 and 23.1-kbp fragments) similar to those obtained previously with Asahipak GS-310 5-microns size-exclusion packings. However, when up to 0.2 M NaCl was added to the solvent, the DNA was increasingly retarded, particularly the 4.4, 6.6 and 9.4-kbp fragments, resulting in improved resolution in the low to middle molecular-mass range. The effect of salt was more significant with Capcell-Pak Phe than C1, although various features characteristic of slalom chromatography were preserved with both columns; i.e., dependency on DNA size, flow-rate, and temperature. This suggests that a mixed mode of separation, that is, slalom mode and hydrophobic-interaction mode, was operating. Although all of the Hypersil-3 packings showed significant adsorption of lambda/HindIII fragments under low-salt conditions, the fragments could be eluted with satisfactory yield and resolution by adding acetonitrile (> 5%) to the solvent. Notably, these Hypersil-3 packings allowed resolution of a 4.4-kbp lambda/HindIII fragment from the flow-through fraction for the first time, possibly due to their small particle size. Thus, various packing materials developed for high-performance liquid chromatography proved to be applicable for slalom chromatography, though the eluting conditions still need to be refined. The results support the concept that slalom chromatography is based on a hydrodynamic phenomenon.
在最近发现的一种用于相对较大DNA分子(> 5 kpb)的新型尺寸分离方法——回转色谱中,通过使用通常用于反相色谱的柱获得了更高的分辨率:即两种类型的Capcell-Pak(甲基或苯基衍生的5微米微珠),以及五种类型的Hypersil-3填料(三甲基硅烷基、二甲基辛基、氰丙基、十八烷基或苯基衍生的3微米微珠)。尽管分离特性有所不同,但使用这些柱时,5-15-kbp DNA的分辨率得到了显著提高。当Capcell-Pak柱与常规低盐洗脱溶剂(10 mM磷酸钠,pH 6.8,1 mM EDTA)一起使用时,获得了λ/HindIII片段(0.1、0.5、2.0、2.3、4.4、6.6、9.4和23.1-kbp片段的混合物)的色谱图,类似于之前使用Asahipak GS-310 5微米尺寸排阻填料获得的色谱图。然而,当向溶剂中加入高达0.2 M NaCl时,DNA的滞留越来越明显,特别是4.4、6.6和9.4-kbp片段,从而在低至中等分子量范围内提高了分辨率。Capcell-Pak Phe柱比C1柱的盐效应更显著,尽管两种柱都保留了回转色谱的各种特征;即对DNA大小、流速和温度的依赖性。这表明存在一种混合分离模式,即回转模式和疏水相互作用模式。尽管所有的Hypersil-3填料在低盐条件下都显示出对λ/HindIII片段的显著吸附,但通过向溶剂中加入乙腈(> 5%),这些片段可以以令人满意的产率和分辨率洗脱。值得注意的是,这些Hypersil-3填料首次从流出级分中分离出了4.4-kbp的λ/HindIII片段,这可能是由于它们的小粒径。因此,尽管洗脱条件仍需优化,但为高效液相色谱开发的各种填料被证明适用于回转色谱。这些结果支持了回转色谱基于流体动力学现象的概念。