Hennessey J P, Scarborough G A
Department of Pharmacology, School of Medicine, University of North Carolina, Chapel Hill 27599.
Anal Biochem. 1989 Feb 1;176(2):284-9. doi: 10.1016/0003-2697(89)90310-2.
A procedure for successful analysis of the hydrophobic tryptic peptides of the Neurospora crassa plasma membrane H+-ATPase by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) is described. The features of this procedure that are essential for the best results include (i) treatment of the hydrophobic peptide samples with neat trifluoroacetic acid, (ii) dissolution and disaggregation of the hydrophobic peptide samples with SDS at 0 degrees C, (iii) SDS-PAGE of the hydrophobic peptide samples in gels containing a 200:1 ratio of acrylamide to bisacrylamide and a 5-20% convex acrylamide gradient, and (iv) silver-staining of the gels after electrophoresis. This method results in the reproducible resolution and visualization of the H+-ATPase hydrophobic tryptic peptides, which range in size from ca. 5 to 21 kDa, as well as other peptides and proteins ranging in size from ca. 2.5 to 150 kDa. The methods described should also prove useful in other studies where resolution and visualization of hydrophobic peptides of integral membrane proteins are required.
描述了一种通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)成功分析粗糙脉孢菌质膜H⁺-ATP酶疏水胰蛋白酶肽的方法。该方法取得最佳结果所必需的特征包括:(i)用纯三氟乙酸处理疏水肽样品;(ii)在0℃下用SDS溶解和分散疏水肽样品;(iii)在含有丙烯酰胺与双丙烯酰胺比例为200:1且丙烯酰胺呈5-20%凸形梯度的凝胶中对疏水肽样品进行SDS-PAGE;(iv)电泳后对凝胶进行银染。该方法可重现地分离并可视化大小约为5至21 kDa的H⁺-ATP酶疏水胰蛋白酶肽,以及大小约为2.5至150 kDa的其他肽和蛋白质。所述方法在其他需要分离和可视化整合膜蛋白疏水肽的研究中也应证明是有用的。