Zieris Andrea, Dockhorn Ron, Röhrich Anika, Zimmermann Ralf, Müller Martin, Welzel Petra B, Tsurkan Mikhail V, Sommer Jens-Uwe, Freudenberg Uwe, Werner Carsten
Leibniz Institute of Polymer Research Dresden , Hohe Strasse 6, 01069 Dresden, Germany.
Biomacromolecules. 2014 Dec 8;15(12):4439-46. doi: 10.1021/bm5012294. Epub 2014 Nov 5.
Sulfation patterns of glycosaminoglycans (GAG) govern the electrostatic complexation of biomolecules and thus allow for modulating the release profiles of growth factors from GAG-based hydrogels. To explore options related to this, selectively desulfated heparin derivatives were prepared, thoroughly characterized, and covalently converted with star-shaped poly(ethylene glycol) into binary polymer networks. The impact of the GAG sulfation pattern on the network characteristics of the obtained hydrogels was theoretically evaluated by mean field methods and experimentally analyzed by rheometry and swelling measurements. Sulfation-dependent differences of reactivity and miscibility of the heparin derivatives were shown to determine network formation. A theory-based design concept for customizing growth factor affinity and physical characteristics was introduced and validated by quantifying the release of fibroblast growth factor 2 from a set of biohybrid gels. The resulting new class of cell-instructive polymer matrices with tunable GAG sulfation will be instrumental for multiple applications in biotechnology and medicine.
糖胺聚糖(GAG)的硫酸化模式决定了生物分子的静电络合作用,从而能够调节基于GAG的水凝胶中生长因子的释放曲线。为了探索与此相关的方法,制备了选择性脱硫酸肝素衍生物,对其进行了全面表征,并将其与星形聚乙二醇共价转化为二元聚合物网络。通过平均场方法从理论上评估了GAG硫酸化模式对所得水凝胶网络特性的影响,并通过流变学和溶胀测量进行了实验分析。结果表明,肝素衍生物的反应性和混溶性的硫酸化依赖性差异决定了网络的形成。引入了一种基于理论的设计概念,用于定制生长因子亲和力和物理特性,并通过量化一组生物杂交凝胶中成纤维细胞生长因子2的释放进行了验证。由此产生的具有可调节GAG硫酸化的新型细胞指导性聚合物基质将有助于生物技术和医学中的多种应用。