Pluen A, Netti P A, Jain R K, Berk D A
Edwin L. Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114 USA.
Biophys J. 1999 Jul;77(1):542-52. doi: 10.1016/S0006-3495(99)76911-0.
The diffusion coefficients (D) of different types of macromolecules (proteins, dextrans, polymer beads, and DNA) were measured by fluorescence recovery after photobleaching (FRAP) both in solution and in 2% agarose gels to compare transport properties of these macromolecules. Diffusion measurements were conducted with concentrations low enough to avoid macromolecular interactions. For gel measurements, diffusion data were fitted according to different theories: polymer chains and spherical macromolecules were analyzed separately. As chain length increases, diffusion coefficients of DNA show a clear shift from a Rouse-like behavior (DG congruent with N0-0.5) to a reptational behavior (DG congruent with N0-2.0). The pore size, a, of a 2% agarose gel cast in a 0.1 M PBS solution was estimated. Diffusion coefficients of the proteins and the polymer beads were analyzed with the Ogston model and the effective medium model permitting the estimation of an agarose gel fiber radius and hydraulic permeability of the gels. Not only did flexible macromolecules exhibit greater mobility in the gel than did comparable-size rigid spherical particles, they also proved to be a more useful probe of available space between fibers.
通过光漂白后荧光恢复(FRAP)技术,在溶液和2%琼脂糖凝胶中测量了不同类型大分子(蛋白质、葡聚糖、聚合物珠和DNA)的扩散系数(D),以比较这些大分子的传输特性。扩散测量在足够低的浓度下进行,以避免大分子间相互作用。对于凝胶测量,扩散数据根据不同理论进行拟合:聚合物链和球形大分子分别进行分析。随着链长增加,DNA的扩散系数呈现出从类似Rouse行为(D∝N^-0.5)到爬行行为(D∝N^-2.0)的明显转变。估算了在0.1 M PBS溶液中浇铸的2%琼脂糖凝胶的孔径a。利用奥格斯顿模型和有效介质模型分析了蛋白质和聚合物珠的扩散系数,从而估算了琼脂糖凝胶纤维半径和凝胶的水力渗透率。柔性大分子不仅在凝胶中比尺寸相当的刚性球形颗粒表现出更大的迁移率,而且还被证明是纤维间可用空间的更有效探针。