Self-regenerating giant hyaluronan polymer brushes
Self-regenerating giant hyaluronan polymer brushes
复制标题
DOI:
10.1038/s41467-019-13440-7
复制
发表时间:
2019-12
影响因子:
16.6
通讯作者:
Wenbin Wei;J. Faubel;Hemaa Selvakumar;Daniel T. Kovari;Joanna Tsao;Felipe Rivas;Amar T. Mohabir;Michelle C Krecker;Elaheh Rahbar;A. Hall;M. Filler;Jennifer L. Washburn;P. Weigel;J. Curtis
中科院分区:
文献类型:
--
作者:
Wenbin Wei;J. Faubel;Hemaa Selvakumar;Daniel T. Kovari;Joanna Tsao;Felipe Rivas;Amar T. Mohabir;Michelle C Krecker;Elaheh Rahbar;A. Hall;M. Filler;Jennifer L. Washburn;P. Weigel;J. Curtis
Tailoring interfaces with polymer brushes is a commonly used strategy to create functional materials for numerous applications. Existing methods are limited in brush thickness, the ability to generate high-density brushes of biopolymers, and the potential for regeneration. Here we introduce a scheme to synthesize ultra-thick regenerating hyaluronan polymer brushes using hyaluronan synthase. The platform provides a dynamic interface with tunable brush heights that extend up to 20 microns – two orders of magnitude thicker than standard brushes. The brushes are easily sculpted into micropatterned landscapes by photo-deactivation of the enzyme. Further, they provide a continuous source of megadalton hyaluronan or they can be covalently-stabilized to the surface. Stabilized brushes exhibit superb resistance to biofilms, yet are locally digested by fibroblasts. This brush technology provides opportunities in a range of arenas including regenerating tailorable biointerfaces for implants, wound healing or lubrication as well as fundamental studies of the glycocalyx and polymer physics.