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采用窄径开口管柱进行流动注射色谱分析。

Performing flow injection chromatography using a narrow open tubular column.

机构信息

Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.

Department of Chemistry, College of Sciences, Northeastern University, Shenyang, 110819, PR China.

出版信息

Anal Chim Acta. 2020 May 1;1109:19-26. doi: 10.1016/j.aca.2020.02.052. Epub 2020 Feb 27.

Abstract

Flow injection chromatography (FIC) or sequential injection chromatography (SIC) is a low-pressure liquid chromatography technique that uses flow injection or sequential injection hardware. Due to the constraints of this hardware, the separation resolution is low; often no more than 3-5 components are resolved. We have recently demonstrated the excellent resolving power of narrow open tubular (OT) columns for various biomolecules, and only moderate elution pressures are needed to carry out these separations. In this paper, we incorporate a narrow OT column with FIC and construct an FIC system using a pressure chamber and two injection valves to implement gradient elution. The resultant system not only improves the resolution but also reduces the system cost. When we use the system to separate peptides from trypsin-digested cytochrome C, we can resolve dozens of peptides (with resolutions of 0.5 or greater) at a speed of 12 samples per hour. When we use this system to separate a mixture containing 3 amino acids, we can base-line resolve these compounds at a speed of 1800 sample per hour.

摘要

流动注射色谱(FIC)或顺序注射色谱(SIC)是一种低压液相色谱技术,使用流动注射或顺序注射硬件。由于这种硬件的限制,分离分辨率较低;通常只能分辨出 3-5 个组分。我们最近证明了窄开口管(OT)柱对各种生物分子具有出色的分辨率,并且仅需要中等的洗脱压力即可进行这些分离。在本文中,我们将窄 OT 柱与 FIC 结合,并使用压力室和两个注射阀构建 FIC 系统以实现梯度洗脱。所得系统不仅提高了分辨率,而且降低了系统成本。当我们使用该系统从胰蛋白酶消化的细胞色素 C 中分离肽时,我们可以以每小时 12 个样品的速度分离数十个肽(分辨率为 0.5 或更高)。当我们使用该系统分离含有 3 种氨基酸的混合物时,我们可以以每小时 1800 个样品的速度基线分离这些化合物。

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