Johansson Christian, Hansson Per, Malmsten Martin
Department of Pharmacy, Uppsala University, P.O. Box 580, SE-751 23 Uppsala, Sweden.
J Colloid Interface Sci. 2007 Dec 15;316(2):350-9. doi: 10.1016/j.jcis.2007.07.052. Epub 2007 Jul 28.
The interaction between lysozyme and oppositely charged poly(acrylic acid) microgels was investigated by micromanipulator-assisted light microscopy, confocal microscopy and circular dichroism. Lysozyme uptake and distribution within the microgel particles, and its effect on microgel deswelling, was studied regarding effects of pH, ionic strength and lysozyme concentration. For a range of conditions, lysozyme distributes nonuniformly within the microgels, forming a lysozyme/microgel shell in the outer parts of the microgel. This shell formation is associated both with increased lysozyme loading to the microgels and with increased lysozyme-induced microgel deswelling. At high microgel charge density, the shell formation displays nonmonotonic ionic strength dependence. The shells formed are characterized by a net positive charge, and by relatively fast exchange of lysozyme between shell and solution, although the exchange kinetics decreases strongly with decreasing ionic strength. At conditions of slower exchange kinetics, the shells are characterized by an effective pore size of less than about 4 nm.
通过微操纵器辅助光学显微镜、共聚焦显微镜和圆二色性研究了溶菌酶与带相反电荷的聚丙烯酸微凝胶之间的相互作用。研究了pH值、离子强度和溶菌酶浓度对溶菌酶在微凝胶颗粒内的摄取和分布及其对微凝胶溶胀的影响。在一系列条件下,溶菌酶在微凝胶内分布不均匀,在微凝胶的外部形成溶菌酶/微凝胶壳。这种壳的形成既与微凝胶中溶菌酶负载量的增加有关,也与溶菌酶诱导的微凝胶溶胀增加有关。在高微凝胶电荷密度下,壳的形成表现出非单调的离子强度依赖性。形成的壳具有净正电荷,并且溶菌酶在壳与溶液之间的交换相对较快,尽管交换动力学随着离子强度的降低而强烈降低。在交换动力学较慢的条件下,壳的有效孔径小于约4nm。