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首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Graphite supported preparation (GSP) of α-Cyano-4-Hydroxycinnamic Acid (CHCA) for matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for peptides and proteins
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Graphite supported preparation (GSP) of α-Cyano-4-Hydroxycinnamic Acid (CHCA) for matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for peptides and proteins

机译:石墨支撑的α-氰基-4-羟基肉桂酸(CHCA)制剂(GSP),用于肽和蛋白质的基质辅助激光解吸/电离质谱(MALDI-MS)

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摘要

Graphite as MALDI matrix or in combination with other substances has been reported in recent years. Here, we demonstrate that graphite can be used as target coating supporting the crystallization of the α-cyano-4- hydroxycinnamic acid matrix. A conventional dried-droplet preparation of matrix and analyte solution on a graphite-coated metal target leads to a thin, uniform layer of cubic crystals with about 1 μm edge length. Commercially available graphite powder of 1-2 μm particle size is gently wiped over the target using a cotton Q-tip, leading to an ultra-thin, not-visible film. This surface modification considerably improves analysis of peptides and proteins for MALDI MS using conventional dried-droplet preparation. Compared with untreated targets, the signal intensities of standard peptides are up to eight times higher when using the graphite supported crystallization. The relative standard deviation in peak area of angiotensin II for sample amounts between 1 and 50 fmol is reduced to about 15 % compared with 45 % for untreated sample holders. For a quantification of 1 fmol of the peptide using an internal standard the coefficient of variation is reduced to 3.5 % from 8 %. The new graphite supported preparation (GSP) protocol is very simple and does not require any technical nor manual skills. All standard solvents for peptides and proteins can be used.
机译:近年来,已经报道了作为MALDI基质或与其他物质组合的石墨。在这里,我们证明了石墨可用作支持α-氰基-4-羟基肉桂酸基质结晶的目标涂层。在涂有石墨的金属靶材上进行基质和分析物溶液的常规干滴制备,会形成边缘长度约为1μm的薄而均匀的立方晶体层。使用棉质Q-tip将市售的1-2μm粒径的石墨粉轻轻擦拭在目标上,形成超薄的不可见薄膜。这种表面修饰大大改善了使用常规干滴制备方法对MALDI MS进行肽和蛋白质分析的能力。与未处理的靶标相比,使用石墨支持的结晶法时,标准肽的信号强度高出八倍。在1至50 fmol之间的样品量中,血管紧张素II峰面积的相对标准偏差降低至约15%,而未处理的样品架则为45%。对于使用内标物定量1 fmol的肽,变异系数从8%降低到3.5%。新的石墨支持的制备(GSP)协议非常简单,不需要任何技术或手工技能。可以使用所有用于肽和蛋白质的标准溶剂。

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