Acetic Acid Enables Precise Tailoring of the Mechanical Behavior of Protein-Based Hydrogels

被引:12
|
作者
Slawinski, Marina [1 ]
Kaeek, Maria [2 ]
Rajmiel, Yair [2 ]
Khoury, Luai R. [2 ]
机构
[1] Univ Wisconsin Milwaukee, Dept Phys, Milwaukee, WI 53211 USA
[2] Technion Israel Inst Technol, Dept Mat Sci & Engn, IL-32000 Haifa, Israel
关键词
Protein-based hydrogels; Biomaterials; Protein folding transitions; Responsive biomaterials; Dynamic hydrogels; CROSS; VISCOELASTICITY; STIFFNESS; MODES; TOUGH;
D O I
10.1021/acs.nanolett.2c01558
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Engineering viscoelastic and biocompatible materials with tailored mechanical and microstructure properties capable of mimicking the biological stiffness (< 17 kPa) or serving as bioimplants will bring protein-based hydrogels to the forefront in the biomaterials field. Here, we introduce a method that uses different concentrations of acetic acid (AA) to control the covalent tyrosine-tyrosine cross-linking interactions at the nanoscale level during protein-based hydrogel synthesis and manipulates their mechanical and microstructure properties without affecting protein concentration and (un)folding nanomechanics. We demonstrated this approach by adding AA as a precursor to the preparation buffer of a photoactivated protein-based hydrogel mixture. This strategy allowed us to synthesize hydrogels made from bovine serum albumin (BSA) and eight repeats protein L structure, with a fine-tailored wide range of stiffness (2-35 kPa). Together with protein engineering technologies, this method will open new routes in developing and investigating tunable protein-based hydrogels and extend their application toward new horizons.
引用
收藏
页码:6942 / 6950
页数:9
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