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在基质辅助激光解吸电离质谱中观察到的蛋白质离子的电荷态分布移动。

Charge state distribution shifting of protein ions observed in matrix-assisted laser desorption ionization mass spectrometry.

机构信息

Division of Immunology, Beckman Research Institute of the City of Hope, 1450 E. Duarte Road, 91010, Duarte, CA.

出版信息

J Am Soc Mass Spectrom. 1995 Dec;6(12):1183-9. doi: 10.1016/1044-0305(95)00578-1.

Abstract

By using a new sample preparation method for matrix-assisted laser desorption ionization, a significant shift to lower mass-to-charge values can be obtained for many protein samples. The sample preparation technique involves the creation of a thin film of protein-doped α-cyano-4-hydroxycinnamic acid (CHCA) matrix formed in the presence of glycerol on top of a previously deposited pad of CHCA matrix. The higher charge states were not observed if the laser power was significantly above the threshold needed to produce protein molecular ions. Similar spectra were observed when samples were prepared in the presence of urea. The phenomenon was specific for the CHCA matrix because no effects were observed when sinapinic acid (3,5-dimethoxy-4-hydroxy-trans-cinnamic acid) and 2-(4-hydroxyphenylazo) benzoic acid matrices were used with the new sample preparation method.

摘要

通过使用一种新的基质辅助激光解吸电离的样品制备方法,可以获得许多蛋白质样品的质量荷比显著向低质量荷比移动的效果。该样品制备技术包括在先前沉积的 CHCA 基质垫上,形成一层由甘油存在下的掺杂有 α-氰基-4-羟基肉桂酸(CHCA)基质的蛋白质的薄膜。如果激光功率显著高于产生蛋白质分子离子所需的阈值,则不会观察到较高的电荷态。当在存在尿素的情况下制备样品时,观察到了相似的光谱。该现象是 CHCA 基质特有的,因为当使用新的样品制备方法时,当使用 3,5-二甲氧基-4-羟基反式肉桂酸(sinapinic 酸)和 2-(4-羟基偶氮)苯甲酸基质时,没有观察到任何影响。

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