Takei Y G, Matsukata M, Aoki T, Sanui K, Ogata N, Kikuchi A, Sakurai Y, Okano T
Department of Chemistry, Faculty of Science and Technology, Sophia University, Tokyo, Japan.
Bioconjug Chem. 1994 Nov-Dec;5(6):577-82. doi: 10.1021/bc00030a013.
Immunoglobulin G (IgG) has been modified by poly(N-isopropylacrylamide) (PIPAAm) to create a novel bioconjugate which exhibits reversible phase transition behavior at 32 degrees C in aqueous media. A terminal carboxyl group introduced into PIPAAm molecule by polymerization of IPAAm with 3-mercaptopropionic acid was used for conjugation to IgG via coupling reaction of activated ester with protein amino group. These conjugates exhibited rapid response to changes in solution temperature and significant phase separation above a critical solution temperature corresponding to that for the original PIPAAm. These conjugates bound to antigen quantitatively in aqueous system, and antigen-bound complex also demonstrated phase separation and precipitation above a critical temperature. Precipitate was reversibly redissolved in cold buffer. Though particular conjugate which includes 12 molecules of PIPAAm with 6,100 molecular weight suppressed more than 95% of Fc-dependent binding with protein A, it retained approximately 60% of original specific antigen binding activity. It was manifested that polymer content of conjugate was 20-30 wt% for the case of 6,100 molecular weight of PIPAAm to demonstrate specific antigen binding activity most effectively and to reduce Fc-dependent binding with protein A. IgG-PIPAAm conjugates were soluble in water and formed antigen-bound complex in homogeneous solution system below a critical temperature. These conjugates were separated from solution and other solutes corresponding to PIPAAm nature and scarcely bound to antigen above a critical temperature. It is revealed that temperature-responsive PIPAAm conjugated to biomolecule operated as a switching molecule. These phenomena are attractive for not only reversible bioreactors and protein separations but also carrier substrate to localize biomolecules such as drugs, peptides and hormones in a living body.
免疫球蛋白G(IgG)已被聚(N-异丙基丙烯酰胺)(PIPAAm)修饰,以制备一种新型生物共轭物,该共轭物在水介质中于32℃表现出可逆的相变行为。通过IPAAm与3-巯基丙酸聚合引入到PIPAAm分子中的末端羧基,用于通过活化酯与蛋白质氨基的偶联反应与IgG共轭。这些共轭物对溶液温度的变化表现出快速响应,并且在高于对应于原始PIPAAm的临界溶液温度时出现明显的相分离。这些共轭物在水性体系中与抗原定量结合,并且抗原结合复合物在临界温度以上也表现出相分离和沉淀。沉淀物在冷缓冲液中可逆地重新溶解。尽管包含12个分子量为6100的PIPAAm分子的特定共轭物抑制了超过95%的与蛋白A的Fc依赖性结合,但它保留了约60%的原始特异性抗原结合活性。结果表明,对于分子量为6100的PIPAAm,共轭物的聚合物含量为20-30 wt%时,能最有效地表现出特异性抗原结合活性并减少与蛋白A的Fc依赖性结合。IgG-PIPAAm共轭物可溶于水,并在低于临界温度的均相溶液体系中形成抗原结合复合物。这些共轭物在临界温度以上与溶液和其他对应于PIPAAm性质的溶质分离,并且几乎不与抗原结合。结果表明,与生物分子共轭的温度响应性PIPAAm起到了开关分子的作用。这些现象不仅对可逆生物反应器和蛋白质分离具有吸引力,而且对在生物体内定位生物分子(如药物、肽和激素)的载体底物也具有吸引力。