Davidova V N, Naberezhnykh G A, Yermak I M, Gorbach V I, Solov'eva T F
Pacific Institute of Bioorganic Chemistry, Far-Eastern Division of the Russian Academy of Sciences, Vladivostok.
Biochemistry (Mosc). 2006 Mar;71(3):332-9. doi: 10.1134/s0006297906030151.
The interaction of endotoxins--lipopolysaccharides (LPS) different in degree of the O-specific chain polymerization--with 20- and 130-kD chitosan was studied using the competitive binding of LPS with the complex of chitosan-anionic dye (tropaeolin 000-2) and the direct binding of (125)I-labeled LPS with chitosan immobilized on Sepharose 4B. The interaction of 20-kD chitosan with LPS was non-cooperative, and immobilization of the polycation on Sepharose resulted in its binding to (125)I-labeled LPS with a positive cooperativity. The interaction of LPS possessing a long O-specific chain with 130-kD chitosan was characterized by negative cooperativity. Binding constants of LPS with the polycation and the number of binding sites per amino group of chitosan were determined. The interaction affinity and stoichiometry of the LPS-chitosan complexes significantly depend on the LPS structure and concentration in the reaction mixture. The increase in the length of carbohydrate chains of LPS results in increase in the binding constants and decrease in the bound endotoxin amount.
利用脂多糖(LPS)与壳聚糖 - 阴离子染料(金莲橙OOO - 2)复合物的竞争性结合以及固定在琼脂糖4B上的壳聚糖与(125)I标记的LPS的直接结合,研究了具有不同O - 特异性链聚合程度的内毒素——脂多糖(LPS)与20kD和130kD壳聚糖的相互作用。20kD壳聚糖与LPS的相互作用是非协同性的,并且将这种聚阳离子固定在琼脂糖上会导致其与(125)I标记的LPS结合呈现正协同性。具有长O - 特异性链的LPS与130kD壳聚糖的相互作用具有负协同性。测定了LPS与聚阳离子的结合常数以及壳聚糖每个氨基的结合位点数。LPS - 壳聚糖复合物的相互作用亲和力和化学计量显著取决于反应混合物中LPS的结构和浓度。LPS碳水化合物链长度的增加导致结合常数增加以及结合的内毒素量减少。