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石墨支持的 α-氰基-4-羟基肉桂酸(CHCA)的制备(GSP)用于肽和蛋白质的基质辅助激光解吸/电离质谱(MALDI-MS)。

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.

机构信息

Institute of Pharmaceutical Chemistry, Cluster of Excellence Macromolecular Complexes, Goethe-University Frankfurt, Frankfurt a M, Germany.

出版信息

J Am Soc Mass Spectrom. 2012 Nov;23(11):1949-54. doi: 10.1007/s13361-012-0478-8. Epub 2012 Sep 20.

DOI:10.1007/s13361-012-0478-8
PMID:22993043
Abstract

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.

摘要

近年来,已有报道称石墨可用作 MALDI 基质或与其他物质联合使用。在此,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靶材涂层。在涂有石墨的金属靶上,通过常规的基质和分析物溶液干滴制备法,可得到具有约 1 μm 边长的薄而均匀的立方晶体层。使用普通的 1-2 μm 粒径的商用石墨粉末,用棉花 Q-tip 轻轻擦拭靶材,即可形成超薄、不可见的薄膜。这种表面修饰极大地改善了使用常规干滴制备法的 MALDI MS 中肽和蛋白质的分析。与未处理的靶材相比,使用石墨支持结晶时,标准肽的信号强度最高可达 8 倍。与未处理的样品支架相比,对于 1 至 50 fmol 之间的样品量,血管紧张素 II 的峰面积的相对标准偏差降低到约 15 %,而未处理的样品支架为 45 %。使用内部标准对 1 fmol 肽进行定量时,变异系数从 8 %降低到 3.5 %。新的石墨支持制备(GSP)方案非常简单,不需要任何技术或手动技能。所有标准的肽和蛋白质溶剂均可使用。

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本文引用的文献

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Mass spectrometry of full-length integral membrane proteins to define functionally relevant structural features.全长整合膜蛋白的质谱分析以确定功能相关的结构特征。
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Ghost peaks observed after atmospheric pressure matrix-assisted laser desorption/ionization experiments may disclose new ionization mechanism of matrix-assisted hypersonic velocity impact ionization.在大气压基质辅助激光解吸/电离实验后观察到的鬼峰可能揭示基质辅助高超音速速度碰撞电离的新电离机制。
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Vibrational analysis of α-cyanohydroxycinnamic acid.α-氰基羟基肉桂酸的振动分析
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Matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometric analysis of intact proteins larger than 100 kDa.大于100 kDa完整蛋白质的基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱分析。
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4-Chloro-alpha-cyanocinnamic acid is an advanced, rationally designed MALDI matrix.4-氯-α-氰基肉桂酸是一种先进的、经过合理设计的基质辅助激光解吸电离(MALDI)基质。
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Analysis of fatty acids by graphite plate laser desorption/ionization time-of-flight mass spectrometry.通过石墨板激光解吸/电离飞行时间质谱法分析脂肪酸。
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Observation of low molecular weight poly(methylsilsesquioxane)s by graphite plate laser desorption/ionization time-of-flight mass spectrometry.用石墨板激光解吸/电离飞行时间质谱法观察低分子量聚(甲基倍半硅氧烷)
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