Assembly-controlled biocompatible interface on a microchip: Strategy to highly efficient proteolysis

被引:50
作者
Liu, Yun
Zhong, Wei
Meng, Sheng
Kong, Jilie
Lu, Haojie
Yang, Pengyuan
Girault, Hubert H.
Liu, Baohong [1 ]
机构
[1] Fudan Univ, Dept Chem, Inst Biomed Sci, Shanghai 200433, Peoples R China
[2] Fudan Univ, Dept Macromol Sci, Shanghai 200433, Peoples R China
[3] Ecole Polytech Fed Lausanne, Lab Electrochim Phys & Analyt, CH-1015 Lausanne, Switzerland
关键词
interfaces; layer-by-layer assembly; microchip reactors; proteomics; trypsin;
D O I
10.1002/chem.200501622
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A biocompatible interface was constructed on a microchip by using the layer-by-layer (LBL) assembly of charged polysaccharides incorporating proteases for highly efficient proteolysis. The controlled assembly of natural polyelectrolytes and the enzyme-adsorption step were monitored by using a quartz-crystal microbalance and atomic force microscopy (AFM). Such a multilayer-assembled membrane provides a biocompatible interconnected network with high enzyme-loading capacity. The maximum digestion rate of the adsorbed trypsin in a microchannel was significantly accelerated to 1600 mm min(-1) mu g(-1), compared with the tryptic digestion in solution. Based on the Langmuir isotherm model, the thermodynamic constant of adsorption K was calculated to be 1.6 x 10(5) M-1 and the maximum adsorption loading Gamma(max) was 3.6 x 10(-6) mol m(-2), 30 times more than a monolayer of trypsin on the native surface. The tunable interface containing trypsin was employed to construct a microchip reactor for digestion of femtomoles of proteins and the produced peptides were analyzed by MALDI-TOF mass spectroscopy. The efficient on-chip proteolysis was obtained within a few seconds, and the identification of biological samples was feasible.
引用
收藏
页码:6585 / 6591
页数:7
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