Al-Lawati Haider, Watts Paul, Welham Kevin J
Department of Chemistry, University of Hull, Cottingham Road, Hull, UKHU6 7RX.
Analyst. 2006 May;131(5):656-63. doi: 10.1039/b600752j. Epub 2006 Mar 22.
A highly efficient protein digestion device has been fabricated using commercially available immobilized trypsin on agarose beads, packed into a silica capillary and connected either directly to an electrospray mass spectrometer via a 'microtight T' connector, from which aqueous acetic acid (0.2%) was pumped, or via a monolithic column connected to the mass spectrometer ion source. Six proteins with molecular mass ranging from 2848 to 77703 Da were digested completely using this system. In the second set of experiments a short monolithic separation column was placed after the immobilized trypsin capillary and partial separation of the generated peptides was obtained. The detection limits were increased from the micromol to pmol range by utilization of this separation column. Gradient elution, using a binary HPLC pump and a flow splitter, was used to optimize the peptide separation. This provided significantly enhanced resolution of the tryptic peptides but increased the analysis time to 30 minutes.
利用琼脂糖珠上的市售固定化胰蛋白酶制造了一种高效蛋白质消化装置,将其填充到硅胶毛细管中,并通过“微密封T”连接器直接连接到电喷雾质谱仪上,从该连接器中泵入0.2%的乙酸水溶液,或者通过连接到质谱仪离子源的整体柱进行连接。使用该系统完全消化了六种分子量范围从2848到77703 Da的蛋白质。在第二组实验中,在固定化胰蛋白酶毛细管之后放置了一个短的整体分离柱,获得了生成肽段的部分分离。通过使用该分离柱,检测限从微摩尔范围提高到皮摩尔范围。使用二元高效液相色谱泵和分流器进行梯度洗脱,以优化肽段分离。这显著提高了胰蛋白酶肽段的分辨率,但将分析时间增加到了30分钟。