Programmable assembly of a metabolic pathway enzyme in a pre-packaged reusable bioMEMS device

被引:46
作者
Luo, Xiaolong [2 ,6 ]
Lewandowski, Angela T. [3 ,4 ]
Yi, Hyunmin [1 ,7 ]
Payne, Gregory F. [4 ]
Ghodssi, Reza [5 ,6 ]
Bentley, William E. [2 ,4 ]
Rubloff, Gary W. [1 ,6 ]
机构
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[3] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20742 USA
[4] Univ Maryland, UMBI, College Pk, MD 20742 USA
[5] Univ Maryland, Dept Elect & Comp Engn, College Pk, MD 20742 USA
[6] Univ Maryland, ISR, College Pk, MD 20742 USA
[7] Tufts Univ, Dept Chem & Biol Engn, Medford, MA 02155 USA
基金
美国国家科学基金会;
关键词
D O I
10.1039/b713756g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report a biofunctionalization strategy for the assembly of catalytically active enzymes within a completely packaged bioMEMS device, through the programmed generation of electrical signals at spatially and temporally defined sites. The enzyme of a bacterial metabolic pathway, S-adenosylhomocysteine nucleosidase (Pfs), is genetically fused with a pentatyrosine "pro-tag" at its C-terminus. Signal responsive assembly is based on covalent conjugation of Pfs to the aminopolysaccharide, chitosan, upon biochemical activation of the pro-tag, followed by electrodeposition of the enzyme-chitosan conjugate onto readily addressable sites in microfluidic channels. Compared to traditional physical entrapment and surface immobilization approaches in microfluidic environments, our signal-guided electrochemical assembly is unique in that the enzymes are assembled under mild aqueous conditions with spatial and temporal programmability and orientational control. Significantly, the chitosan-mediated enzyme assembly can be reversed, making the bioMEMS reusable for repeated assembly and catalytic activity. Additionally, the assembled enzymes retain catalytic activity over multiple days, demonstrating enhanced enzyme stability. We envision that this assembly strategy can be applied to rebuild metabolic pathways in microfluidic environments for antimicrobial drug discovery.
引用
收藏
页码:420 / 430
页数:11
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