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使用增强流动性液相色谱法进行蛋白质分离。

Protein separations using enhanced-fluidity liquid chromatography.

作者信息

Bennett Raffeal, Olesik Susan V

机构信息

Department of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH 43210, United States.

Department of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH 43210, United States.

出版信息

J Chromatogr A. 2017 Nov 10;1523:257-264. doi: 10.1016/j.chroma.2017.07.060. Epub 2017 Jul 22.

Abstract

Enhanced-fluidity liquid chromatography (EFLC) methods using methanol/HO/CO and hydrophilic interaction liquid chromatography (HILIC) were explored for the separation of proteins and peptides. EFLC is a separation mode that uses a mobile phase made of conventional solvents combined with liquid carbon dioxide (CO) in subcritical conditions. The addition of liquid CO enhances diffusivity and decreases viscosity while maintaining mixture polarity, which typically results in reduced time of analysis. TFA additive and elevated temperature were leveraged as key factors in the separation of a 13-analyte intact protein mixture in under 5min. Under these conditions EFLC showed modest improvement in terms of peak asymmetry and analysis time over the competing ACN/HO separation. Protein analytes detected by electrospray ionization - quadrupole time of flight, were shown to be unaffected by the addition of CO in the mobile phase. Herein, the feasibility of separating hydrophilic proteins up to 80kDa (with transferrin) is demonstrated for CO-containing mobile phases.

摘要

探索了使用甲醇/水/二氧化碳的增强流动性液相色谱(EFLC)方法和亲水相互作用液相色谱(HILIC)来分离蛋白质和肽。EFLC是一种分离模式,它使用由常规溶剂与处于亚临界条件的液态二氧化碳(CO₂)组成的流动相。添加液态CO₂可提高扩散率并降低粘度,同时保持混合物极性,这通常会缩短分析时间。在5分钟内分离13种分析物的完整蛋白质混合物时,三氟乙酸添加剂和升高的温度被用作关键因素。在这些条件下,与竞争性的乙腈/水分离相比,EFLC在峰不对称性和分析时间方面有适度改善。通过电喷雾电离-四极杆飞行时间检测的蛋白质分析物不受流动相中添加CO₂的影响。本文证明了含CO₂流动相分离高达80kDa亲水性蛋白质(包括转铁蛋白)的可行性。

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