明胶
材料科学
结合
软物质
组织谷氨酰胺转胺酶
纳米技术
基质(化学分析)
赖氨酸
酶
谷氨酰胺
化学工程
组合化学
生物物理学
生物化学
化学
有机化学
氨基酸
生物
工程类
数学分析
数学
胶体
复合材料
作者
Yi Liu,Jessica L. Terrell,Chen‐Yu Tsao,Hsuan‐Chen Wu,Vishal Javvaji,Eunkyoung Kim,Yi Cheng,Yifeng Wang,Rein V. Ulijn,Srinivasa R. Raghavan,Gary W. Rubloff,William E. Bentley,Gregory Francis Payne
标识
DOI:10.1002/adfm.201200095
摘要
Abstract Methods that allow soft matter to be fabricated with controlled structure and function would be beneficial for applications ranging from flexible electronics to regenerative medicine. Here, the assembly of a multifunctional gelatin matrix is demonstrated by triggering its self‐assembly and then enzymatically assembling biological functionality. Triggered self‐assembly relies on electrodeposition of the pH‐responsive hydrogelator, 9‐fluorenylmethoxycarbonyl‐phenylalanine (Fmoc‐Phe), in response to electrical inputs that generate a localized pH‐gradient. Warm solutions of Fmoc‐Phe and gelatin are co‐deposited and, after cooling to room temperature, a physical gelatin network forms. Enzymatic assembly employs the cofactor‐independent enzyme microbial transglutaminase (mTG) to perform two functions: crosslink the gelatin matrix to generate a thermally stable chemical gel and conjugate proteins to the matrix. To conjugate globular proteins to gelatin these proteins are engineered to have short lysine‐rich or glutamine‐rich fusion tags to provide accessible residues for mTG‐catalysis. Viable bacteria can be co‐deposited and entrapped within the crosslinked gelatin matrix and can proliferate upon subsequent incubation. These results demonstrate the potential for enlisting biological materials and mechanisms to biofabricate multifunctional soft matter.
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