Volume 24, Issue 7 pp. 903-909
Full Paper

Sol-gel-derived Poly(dimethylsiloxane) Enzymatic Reactor for Microfluidic Peptide Mapping

Hui-Ling Wu

Hui-Ling Wu

School of Pharmacy, Second Military Medical University, the People's Liberation Army, Shanghai 200433, China

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Peng-Yuan Yang

Peng-Yuan Yang

Department of Chemistry, Research Center for Proteome, Fudan University, Shanghai 200433, China

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Guo-Rong Fan

Guo-Rong Fan

Project supported by the National Natural Science Foundation of China (Nos. 30572227, 20299030), Shanghai Science Research Foundation (No. 03JC14005), National Basic Research Priority Program (No. 001CB510202) and National High Technology Key Project (No. 2002BAC11A11).

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Yu-Ping Tian

Yu-Ping Tian

Department of Chemistry, Research Center for Proteome, Fudan University, Shanghai 200433, China

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Hao-Jie Lu

Hao-Jie Lu

Department of Chemistry, Research Center for Proteome, Fudan University, Shanghai 200433, China

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Hong Jin

Hong Jin

Department of Chemistry, Research Center for Proteome, Fudan University, Shanghai 200433, China

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First published: 04 July 2006
Citations: 4

Abstract

The silica-based poly(dimethylsiloxane) (PDMS) microfluidic enzymatic reactor was reported along with its analytical features in coupling with MALDI TOF and ESI MS. Microfluidic chip was fabricated using PDMS casting and O2-plasma techniques, and used for the preparation of enzymatic reactor. Plasma oxidation for PDMS enabled the channel wall of microfluidics to present a layer of silanol (SiOH) groups. These SiOH groups as anchors onto the microchannel wall were linked covalently with the hydroxy groups of trypsin-encapsulated sol matrix. As a result, the leakage of sol-gel matrix from the microchannel was effectively prevented. On-line protein analysis was performed with the microfluidic enzymatic reactor by attachment of stainless steel tubing electrode and replaceable tip. The success of trypsin encapsulation was investigated by capillary electrophoresis (CE) detection, and MALDI TOF and ESI MS analysis. The lab-made device provided excellent extent of digestion even at the fast flow rate of 7.0 (L/min with very short residence time of ca. 2 s. In addition, the encapsulated trypsin exhibits increased stability even after continuous use. These features are the most requisite for high-throughput protein identification.

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