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酸性粘多糖及酸性粘多糖-蛋白质对胶原蛋白溶液中纤维形成的影响。

The effect of acid mucopolysaccharides and acid mucopolysaccharide-proteins on fibril formation from collagen solutions.

作者信息

Mathews M B, Decker L

出版信息

Biochem J. 1968 Oct;109(4):517-26. doi: 10.1042/bj1090517.

DOI:10.1042/bj1090517
PMID:4234698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1186937/
Abstract
  1. The effects of acid mucopolysaccharides and acid mucopolysaccharide-proteins on the size and rate of formation of fibril aggregates from collagen solutions in pH7.6 buffers were studied by turbidimetric and light-scattering methods. 2. Serum albumin, orosomucoid, methylated cellulose, chondroitin sulphate A and chondroitin sulphate C of molecular weight less than 20000, and hyaluronate of molecular weight less than 40000 did not influence rates of fibril formation. Chondroitin sulphate A, chondroitin sulphate C and hyaluronate of high molecular weight retarded the rate of fibril formation. This effect of high-molecular-weight chondroitin sulphate C decreased with increasing ionic strength. Heparin, though of low molecular weight (13000), was highly effective, as was also heparitin sulphate. The chondroitin sulphate-proteins of very high molecular weight were highly effective, despite the fact that for some preparations the component chondroitin sulphate chains had molecular weights much less than 20000. 3. Agents that had delayed fibril formation were also effective in producing an increase in degree of aggregation of fibrillar collagen, as indicated by dissymmetry changes observed in light-scattering experiments at low collagen concentrations. Methylated cellulose and heparin at 2.5mug./ml. were unusual in decreasing aggregation, but heparin at 0.25mug./ml. increased aggregation. Electron microscopy of gels showed fibrils and fibril aggregates with ;normal' collagen spacing and dimensions consistent with the light-scattering results. 4. The rates of electrical transport of agents and of solvent (electro-osmosis) through collagen gels indicated a contribution of molecular entanglement that increased with increase in molecular size of the agents. Electrostatic binding of heparin to collagen was noted. Binding to collagen during fibril formation was also found for heparitin sulphate and a chondroitin sulphate with extra sulphate groups. 5. Electrostatic binding of acid mucopolysaccharide-proteins to collagen may be an important factor in the organization and functioning of connective tissues at all stages of growth and development. Excluded-volume (molecular-entanglement) effects may also be important. These factors operate simultaneously and interact mutually so that precise assessment of their relative importance is difficult.
摘要
  1. 采用比浊法和光散射法研究了酸性粘多糖及酸性粘多糖 - 蛋白对pH7.6缓冲液中胶原蛋白溶液形成原纤维聚集体的大小和速率的影响。2. 血清白蛋白、类粘蛋白、甲基化纤维素、分子量小于20000的硫酸软骨素A和硫酸软骨素C以及分子量小于40000的透明质酸盐不影响原纤维形成速率。高分子量的硫酸软骨素A、硫酸软骨素C和透明质酸盐会延缓原纤维形成速率。高分子量硫酸软骨素C的这种作用随离子强度增加而减弱。肝素虽然分子量低(13000),但非常有效,硫酸类肝素也是如此。极高分子量的硫酸软骨素 - 蛋白非常有效,尽管对于某些制剂,其组成的硫酸软骨素链的分子量远小于20000。3. 如在低胶原蛋白浓度下光散射实验中观察到的不对称性变化所示,延迟原纤维形成的试剂在增加纤维状胶原蛋白的聚集程度方面也很有效。2.5μg/ml的甲基化纤维素和肝素在降低聚集方面不寻常,但0.25μg/ml的肝素会增加聚集。凝胶的电子显微镜检查显示原纤维和原纤维聚集体具有“正常”的胶原间距和尺寸,与光散射结果一致。4. 试剂和溶剂(电渗)通过胶原凝胶的电迁移速率表明分子缠结的作用随着试剂分子大小的增加而增加。注意到肝素与胶原的静电结合。在原纤维形成过程中,硫酸类肝素和具有额外硫酸基团的硫酸软骨素也被发现与胶原结合。5. 酸性粘多糖 - 蛋白与胶原的静电结合可能是结缔组织在生长和发育的所有阶段的组织和功能中的一个重要因素。排除体积(分子缠结)效应也可能很重要。这些因素同时起作用并相互影响,因此难以精确评估它们的相对重要性。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/1186937/11dca3260bc9/biochemj00717-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/1186937/11dca3260bc9/biochemj00717-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/1186937/11dca3260bc9/biochemj00717-0040-a.jpg

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