Sinha P, Poland J, Schnölzer M, Rabilloud T
Institut für Laboratoriumsmedizin und Pathobiochemie, Universitätsklinikum Charité, Campus Charité Mitte, Schumannstrasse 20-21, 10117 Berlin, Germany.
Proteomics. 2001 Jul;1(7):835-40. doi: 10.1002/1615-9861(200107)1:7<835::AID-PROT835>3.0.CO;2-2.
We report on a new silver stain especially developed for staining large gels (25 cm x 20 cm) from the Hoefer ISO-DALT system for matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) analysis of proteins. The staining protocol can be summarized as follows: the gels are sensitised in tetrathionate/potassium acetate solution and washed several times in distilled water. After impregnation with silver nitrate, the silver is reduced in the presence of potassium carbonate, thiosulphate and formaldehyde. The staining procedure is stopped with Tris/acetate after which the gels are rinsed and stored in water before spot picking for MALDI-TOF analysis is performed. This protocol has several advantages over existing ones. The gels are stained in a new apparatus that reduces gel handling to a minimum thus also reducing the contamination with keratins to a minimum. The development times in potassium carbonate are very long (up to 40 min) thus improving batch-to-batch reproducibility. Only the surface of the proteins is stained and the silver can be oxidized, thereafter MALDI-TOF can be performed with protein loads as little as 100 micrograms per gel.
我们报道了一种专门为从霍夫尔ISO - DALT系统中对用于蛋白质基质辅助激光解吸/电离飞行时间(MALDI - TOF)分析的大型凝胶(25厘米×20厘米)进行染色而开发的新型银染法。染色方案总结如下:凝胶在连四硫酸盐/醋酸钾溶液中敏化,然后在蒸馏水中洗涤数次。用硝酸银浸渍后,在碳酸钾、硫代硫酸盐和甲醛存在的情况下使银还原。用Tris/醋酸盐终止染色过程,之后冲洗凝胶并保存在水中,然后进行用于MALDI - TOF分析的斑点挑选。该方案相对于现有方案具有多个优点。凝胶在一种新装置中染色,该装置将凝胶处理降至最低限度,从而也将角蛋白污染降至最低限度。在碳酸钾中的显色时间非常长(长达40分钟),从而提高了批次间的重现性。仅蛋白质表面被染色且银可被氧化,此后每块凝胶仅需100微克蛋白质负载量即可进行MALDI - TOF分析。