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具有已知微观几何结构的多孔材料中蛋白质的传输速率。

Transport rates of proteins in porous materials with known microgeometry.

作者信息

Saltzman W M, Langer R

机构信息

Harvard/MIT Division of Health Sciences and Technology, Cambridge, Massachusetts 02139.

出版信息

Biophys J. 1989 Jan;55(1):163-71. doi: 10.1016/S0006-3495(89)82788-2.

Abstract

Many biological and biotechnological systems involve the diffusion of macromolecules through complicated macroporous (pore size on the order of 10-100 microns) environments. In this report, we present and evaluate an experimental system for measuring the rate of protein transport in an inert, macroporous membrane. For this particular membrane system, the microgeometry was characterized in terms of distribution of pore size, position, and orientation. Although the rate of protein desorption was much less than expected based on continuum diffusion models, we demonstrate that the measured transport rates are consistent with diffusion of protein in a complex, interconnected network of water-filled pores. The porous systems exhibit transitional behavior in quantitative agreement with the behavior of percolation lattices (mean square error 7%, n = 29). Predictive mathematical models of the diffusion process were developed: these models used percolation concepts to describe pore topology, continuum models of diffusion/dissolution to describe protein movement at each single pore, and measured pore size distributions. Effective diffusion coefficients for protein transport in aqueous, constricted macropores were predicted by this technique. Predicted diffusion coefficients, based on measured and derived microstructural parameters, agree with experimentally measured diffusion coefficients within a factor of 2. This approach may be useful in the design of porous polymer systems for biological applications and for evaluating other biological systems where conduction of mass, heat, momentum, or charge occurs in a heterogeneous environment.

摘要

许多生物和生物技术系统都涉及大分子在复杂的大孔(孔径在10 - 100微米量级)环境中的扩散。在本报告中,我们展示并评估了一个用于测量蛋白质在惰性大孔膜中传输速率的实验系统。对于这个特定的膜系统,微观几何结构通过孔径分布、位置和取向来表征。尽管基于连续介质扩散模型,蛋白质解吸速率远低于预期,但我们证明所测得的传输速率与蛋白质在充满水的相互连通的复杂孔网络中的扩散是一致的。多孔系统表现出的过渡行为与渗流晶格的行为在定量上相符(均方误差7%,n = 29)。我们开发了扩散过程的预测数学模型:这些模型使用渗流概念来描述孔拓扑结构,用扩散/溶解的连续介质模型来描述每个单个孔中蛋白质的运动,并结合测量得到的孔径分布。通过该技术预测了蛋白质在含水的收缩大孔中传输的有效扩散系数。基于测量和推导的微观结构参数预测的扩散系数与实验测量的扩散系数在2倍的范围内相符。这种方法可能有助于设计用于生物应用的多孔聚合物系统,以及评估其他在非均匀环境中发生质量、热量、动量或电荷传导的生物系统。

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