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Determination of Second Virial Coefficient of Proteins Using a Dual-Detector Cell for Simultaneous Measurement of Scattered Light Intensity and Concentration in SEC-HPLC

机译:使用双检测池同时测量SEC-HPLC中散射光强度和浓度的蛋白质的第二病毒系数的测定

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摘要

A method is proposed for the measurement of the B22 value of proteins in aqueous solutions in flow-mode that utilizes a novel fabricated dual-detector cell, which simultaneously measures protein concentration and the corresponding scattered light intensity at 90°, after the protein elutes from a size-exclusion column. Each data point on the chromatograms obtained from the light scattering detector and the concentration (ultraviolet) detector is converted to Rayleigh's ratio, Rθ, and concentration, c, respectively. The B22 value is calculated from the slope of the Debye plot (Kc/Rθ versus c) generated from a range of concentrations obtained from these chromatograms for a single protein injection. It is shown that this method provides reliable determination of the B22 values for such proteins as lysozyme, chymotrypsinogen, and chymotrypsin in various solution conditions that agree well with those reported in literature.
机译:提出了一种以流动模式测量水溶液中蛋白质B22值的方法,该方法利用新型制造的双检测器池,在蛋白质从中洗脱出来后,同时测量蛋白质浓度和相应的90°散射光强度。尺寸排除列。从光散射检测器和浓度(紫外线)检测器获得的色谱图上的每个数据点分别转换为瑞利比Rθ和浓度c。 B22值是根据德比曲线的斜率(Kc /Rθ对c)计算得出的,该斜率是从这些色谱图获得的单次蛋白质注射所获得的一系列浓度范围内得出的。结果表明,该方法可以可靠地确定溶菌酶,胰凝乳蛋白酶原和胰凝乳蛋白酶等蛋白质在各种溶液条件下的B22值,这些条件与文献报道的方法非常吻合。

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