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Chip-Type Asymmetrical Flow Field-Flow Fractionation Channel Coupled with Mass Spectrometry for Top-Down Protein Identification

机译:芯片型非对称流场-流分馏通道与质谱联用,用于自上而下的蛋白质鉴定

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摘要

A chip-type design asymmetrical flow field-flow fractionation (AF4) channel has been developed for high-speed separation of proteins and top-down proteomic analysis using online coupled electrospray ionization mass spectrometry (ESI-MS). The new miniaturized AF4 channel was assembled by stacking multilayer thin stainless steel (SS, 1.5 mm each) plates embedded with an SS frit in such a way that the total thickness of the channel assembly was about 6 mm. The efficiency of the miniaturized AF4 channel at different channel lengths was examined with the separation of protein standards by adjusting flow rates in which an identical effective channel flow rate or an identical void time can be maintained at different channels. Detection limit, overloading effect, reproducibility, and influence of channel membrane materials on separation efficiency were investigated. Desalting and purification of proteins achieved during the AF4 operation by the action of an exiting crossflow and the use of aqueous mass-spectrometry-compatible (MS-compatible) buffer were advantageous for online coupling of the chip-type AF4 with ESI-MS. The direct coupling of AF4 and ESI-MS capabilities was demonstrated for the high-speed separation and identification of carbonic anhydrase (29 kDa) and transferrin (78 kDa) by full scan MS and for the first top-down identification of proteins with AF4-ESI-MS-MS using collision-induced fragmentation (CID). The presence of intact dimers (156 kDa) of transferrin was confirmed by AF4-ESI-MS via size separation of the dimers from monomers, followed by multiply charged ion spectral analysis of the dimers and molecular mass determinations. It was also found from these experiments that AF4-ESI-MS analysis of transferrin exhibited an increased signal-to-noise ratio compared to that of direct ESI-MS analysis due to online purification of the protein sample and size separation of dimers with AF4.
机译:已经开发了一种芯片型设计的非对称流场流分馏(AF4)通道,用于使用在线耦合电喷雾电离质谱(ESI-MS)进行蛋白质的高速分离和自上而下的蛋白质组学分析。新的小型化AF4通道是通过堆叠嵌入SS熔块的多层薄不锈钢板(SS,每个1.5 mm)组装而成的,以使通道组件的总厚度约为6 mm。通过调节流速,通过在不同的通道长度下保持相同的有效通道流速或相同的无效时间,可以通过分离蛋白质标准品来检查微型化AF4通道在不同通道长度下的效率。研究了检测限,过载效应,重现性以及通道膜材料对分离效率的影响。在AF4操作过程中,通过存在的横流作用进行脱盐和纯化蛋白质,以及使用水相质谱兼容(MS兼容)缓冲液有利于将芯片型AF4与ESI-MS在线偶联。通过全扫描MS可以快速分离和鉴定碳酸酐酶(29 kDa)和转铁蛋白(78 kDa),以及通过AF4首次自上而下地鉴定蛋白质,证明了AF4和ESI-MS功能的直接结合。使用碰撞诱导碎片(CID)的ESI-MS-MS。 AF4-ESI-MS通过将二聚体与单体进行大小分离,然后对二聚体进行多电荷离子光谱分析和分子量测定,通过AF4-ESI-MS确认了转铁蛋白完整二聚体(156 kDa)的存在。从这些实验中还发现,由于蛋白质样品的在线纯化和AF4对二聚体的大小分离,与直接ESI-MS分析相比,转铁蛋白的AF4-ESI-MS分析显示出更高的信噪比。

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