Shogren R L, Blackwell J, Jamieson A M, Carrino D A, Pechak D, Caplan A I
J Biol Chem. 1983 Dec 25;258(24):14741-4.
Static and dynamic light-scattering methods have been used to investigate the structure of chick limb bud chondrocyte proteoglycan aggregate in 0.4 M guanidinium chloride. Zimm plot data for proteoglycan aggregate yield a molecular weight of 45 +/- 8 X 10(6) which compares well with a value of approximately 43 X 10(6) obtained by combination of the diffusion and sedimentation data via the Svedberg equation. The molecular weight of the proteoglycan subunit was determined previously to be 1.4 +/- 0.3 X 10(6), which indicates that the average proteoglycan aggregate molecule contains 32 associated subunits. This is in good agreement with electron microscopy which suggests an average of approximately 25.5 subunits/aggregate; it can be concluded that the aggregates visualized by electron microscopy are also present in solution. These data are also compatible with the ratio of the hydrodynamic volumes of proteoglycan aggregate and subunit. The formation of the aggregate structure has little effect on the solvent-binding capacity of the components: both proteoglycan aggregate and subunit have expanded coil conformations that include approximately 99% solvent.
静态和动态光散射方法已被用于研究鸡胚肢芽软骨细胞蛋白聚糖聚集体在0.4M氯化胍中的结构。蛋白聚糖聚集体的 Zimm 图数据得出分子量为45±8×10⁶,这与通过 Svedberg 方程结合扩散和沉降数据得到的约43×10⁶的值相当吻合。蛋白聚糖亚基的分子量先前测定为1.4±0.3×10⁶,这表明平均蛋白聚糖聚集体分子包含32个相关亚基。这与电子显微镜观察结果非常一致,电子显微镜观察表明平均约25.5个亚基/聚集体;可以得出结论,电子显微镜观察到的聚集体在溶液中也存在。这些数据也与蛋白聚糖聚集体和亚基的流体力学体积比相符。聚集体结构的形成对组分的溶剂结合能力影响很小:蛋白聚糖聚集体和亚基都具有扩展的卷曲构象,其中约99%为溶剂。