Customizing Morphology, Size, and Response Kinetics of Matrix Metalloproteinase-Responsive Nanostructures by Systematic Peptide Design

被引:49
|
作者
Son, Jiye [1 ,2 ,3 ]
Kalafatovic, Daniela [1 ]
Kumar, Mohit [1 ]
Yoo, Barney [5 ]
Cornejo, Mike A. [2 ]
Contel, Maria [2 ,3 ,4 ]
Ulijn, Rein V. [1 ,3 ,5 ]
机构
[1] CUNY, Adv Sci Res Ctr, Grad Ctr, 85 St Nicholas Terrace, New York, NY 10031 USA
[2] CUNY Brooklyn Coll, Dept Chem, 2900 Bedford Ave, Brooklyn, NY 11210 USA
[3] CUNY, Grad Ctr, PhD Program Chem, 365 Fifth Ave, New York, NY 10016 USA
[4] CUNY, Grad Ctr, PhD Program Biochem, 365 Fifth Ave, New York, NY 10016 USA
[5] CUNY Hunter Coll, Dept Chem, 695 Pk Ave, New York, NY 10065 USA
关键词
MMP-responsive; enzyme kinetics; electrostatic enzyme interactions; supramolecular organization; morphology change; self-assembling peptides; BIOMATERIALS; DEGRADATION; HYDROLYSIS; CLEAVAGE; DELIVERY; RELEASE; TARGETS; SITES;
D O I
10.1021/acsnano.8b07401
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Overexpression and activation of matrix metalloproteinase-9 (MMP-9) is associated with multiple diseases and can serve as a stimulus to activate nanomaterials for sensing and controlled release. In order to achieve autonomous therapeutics with improved spacetime targeting capabilities, several features need to be considered beyond the introduction of an enzyme cleavable linker into a nanostructure. We introduce guiding principles for a customizable platform using supra molecular peptide nanostructures with three modular components to achieve tunable kinetics and morphology changes upon MMP-9 exposure. This approach enables (1) fine-tuning of kinetics through introduction of ordered/disordered structures, (2) a 12-fold variation in hydrolysis rates achieved by electrostatic (mis)matching of particle and enzyme charge, and (3) selection of enzymatic reaction products that are either cell-killing nanofibers or disintegrate. These guiding principles, which can be rationalized and involve exchange of just a few amino acids, enable systematic customization of enzyme-responsive peptide optimization of enzyme responsive materials.
引用
收藏
页码:1555 / 1562
页数:8
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