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通过微滤从转基因山羊奶中优化单克隆抗体的回收。

Optimized recovery of monoclonal antibodies from transgenic goat milk by microfiltration.

作者信息

Baruah Gautam Lal, Belfort Georges

机构信息

Howard P. Isermann Department of Chemical Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.

出版信息

Biotechnol Bioeng. 2004 Aug 5;87(3):274-85. doi: 10.1002/bit.20112.

Abstract

The Predictive Aggregate Transport Model for microfiltration is used in combination with optimum fluid mechanics and electrostatics to maximize recovery of a heterologous immunoglobulin (IgG) from transgenic goat milk. The optimization algorithm involved varying pH (6.8-9), transmembrane pressure (2-4.5 psi), milk feed concentration (1-2X), membrane module type (linear vs. helical design), and axial velocity (Reynolds number: 830-1170). Operation in the pressure-dependent regime at low uniform transmembrane pressures (approximately 2 psi) using permeate circulation in co-flow, at the pI of the protein (9 in this case) was used to increase IgG recovery from less than 1% to over 95%. Sodium dodecyl sulfate polyacrylamide gel electrophoresis and attenuated total reflection Fourier transform infrared spectroscopy of the microfiltration permeate samples confirmed that all the fat globules and most of the casein micelles were retained in the MF membrane whereas a large amount of the target IgG was transported through the membrane. Transmembrane pressure and hence permeation flux was kept low (approximately 15 lmh) to maximize IgG membrane transport and thus recovery, due to a sparse deposit on the membrane which facilitated high solute transport. Next, an analytical method was used to optimize the diafiltration process using the aggregate transport model, experimental target protein sieving coefficients and permeation flux (Baruah and Belfort, 2003). The methodology reported here should be generalizable to the recovery of target proteins found in other complex suspensions of biological origin using the microfiltration process.

摘要

微滤的预测性聚集传输模型与最佳流体力学和静电学相结合,以最大限度地从转基因山羊奶中回收异源免疫球蛋白(IgG)。优化算法涉及改变pH值(6.8 - 9)、跨膜压力(2 - 4.5 psi)、牛奶进料浓度(1 - 2X)、膜组件类型(线性与螺旋设计)和轴向速度(雷诺数:830 - 1170)。在低均匀跨膜压力(约2 psi)下的压力依赖模式下操作,采用并流渗透循环,在蛋白质的pI值(在这种情况下为9)下,可将IgG回收率从低于1%提高到超过95%。微滤渗透样品的十二烷基硫酸钠聚丙烯酰胺凝胶电泳和衰减全反射傅里叶变换红外光谱证实,所有脂肪球和大部分酪蛋白胶束都保留在微滤膜中,而大量目标IgG则透过膜传输。由于膜上沉积物稀疏,有利于高溶质传输,因此跨膜压力和渗透通量保持较低(约15 lmh),以最大限度地提高IgG的膜传输及回收率。接下来,使用一种分析方法,利用聚集传输模型、实验目标蛋白筛分系数和渗透通量来优化渗滤过程(Baruah和Belfort,2003)。本文报道的方法应可推广应用于通过微滤过程从其他生物来源的复杂悬浮液中回收目标蛋白。

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