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三叶草形毛细管通道聚合物纤维柱与表面多孔和整体相的比较分析,用于反相蛋白质分离。

Comparative analysis of trilobal capillary-channeled polymer fiber columns with superficially porous and monolithic phases toward reversed-phase protein separations.

机构信息

Department of Chemistry, Biosystems Research Complex, Clemson University, Clemson, South Carolina, USA.

出版信息

J Sep Sci. 2022 Oct;45(20):3811-3826. doi: 10.1002/jssc.202200410. Epub 2022 Aug 26.

Abstract

A trilobal capillary-channeled polymer fiber stationary phase is evaluated for its performance for intact protein separations under reversed-phase high-performance liquid chromatography conditions. The separation quality, operational characteristics, and protein dynamic loading capacity on the fiber phases are compared to commercially-available superficially porous and monolithic columns. The trilobal or "y-shaped" polypropylene fiber phase was employed to separate a synthetic mixture of five proteins (having diverse chemistries and molecular weights). The separation quality was evaluated based on the resolution, peak heights/recoveries, peak widths, and peak areas. The present work illustrates the unique ability to operate at higher linear velocities (47.5 mm/s) while maintaining lower back pressures (∼4 MPa), faster separation times (<8 min), and faster gradient rates using the fiber columns while yielding comparable chromatographic performance to the commercial columns. The separations employing the commercial stationary phases operate at lower linear velocities (∼3.0 mm/s), higher back pressures (∼9 MPa), require longer separation times (10 min), and require slightly higher compositions of organic mobile phase to effect protein elution. Likewise, based on breakthrough loading analysis of lysozyme and bovine serum albumin, the trilobal, polypropylene C-CP fiber column stationary phases demonstrate 3-9X greater binding capacities on a bed volume basis versus the commercial columns.

摘要

一种三叶形毛细管通道聚合物纤维固定相,用于在反相高效液相色谱条件下评估其用于完整蛋白质分离的性能。比较了纤维相的分离质量、操作特性和蛋白质动态上样容量与市售的表面多孔和整体柱。三叶形或“Y 形”聚丙烯纤维相用于分离五种具有不同化学性质和分子量的蛋白质的合成混合物。根据分辨率、峰高/回收率、峰宽和峰面积评估分离质量。本工作说明了在使用纤维柱时以更高的线性速度(47.5mm/s)操作而同时保持更低的背压(约 4MPa)、更快的分离时间(<8 分钟)和更快的梯度速率的独特能力,同时产生可与商业柱相媲美的色谱性能。使用商业固定相的分离在较低的线性速度(约 3.0mm/s)、较高的背压(约 9MPa)下进行,需要更长的分离时间(10 分钟),并且需要稍微更高的有机流动相组成来实现蛋白质洗脱。同样,基于溶菌酶和牛血清白蛋白的穿透负载分析,三叶形、聚丙烯 C-CP 纤维柱固定相在床体积基础上表现出比商业柱高 3-9 倍的结合能力。

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