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DOI 10.1016/j.jasms.2008.03.015

Медицинская библиотека · Journal of the American Society for Mass Spectrometry · 2008

Development of an automated digestion and droplet deposition microfluidic chip for MALDI-TOF MS.

Lee Jeonghoon, Musyimi Harrison K, Soper Steven A, Murray Kermit K

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Аннотация

An automated proteolytic digestion bioreactor and droplet deposition system was constructed with a plastic microfluidic device for off-line interfacing to matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The microfluidic chips were fabricated in poly(methyl methacrylate) (PMMA), using a micromilling machine and incorporated a bioreactor, which was 100 microm wide, 100 microm deep, and possessed a 4 cm effective channel length (400 nL volume). The chip was operated by pressure-driven flow and mounted on a robotic fraction collector system. The PMMA bioreactor contained surface immobilized trypsin, which was covalently attached to the UV-modified PMMA surface using coupling reagents N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) and hydroxysulfosuccinimide (sulfo-NHS). The digested peptides were mixed with a MALDI matrix on-chip and deposited as discrete spots on MALDI targets. The bioreactor provided efficient digestion of a test protein, cytochrome c, at a flow rate of 1 microL/min, producing a reaction time of approximately 24 s to give adequate sequence coverage for protein identification. Other proteins were also evaluated using this solid-phase bioreactor. The efficiency of digestion was evaluated by monitoring the sequence coverage, which was 64%, 35%, 58%, and 47% for cytochrome c, bovine serum albumin (BSA), myoglobin, and phosphorylase b, respectively.

Для цитирования: Lee Jeonghoon, Musyimi Harrison K, Soper Steven A, Murray Kermit K. Development of an automated digestion and droplet deposition microfluidic chip for MALDI-TOF MS.. Journal of the American Society for Mass Spectrometry. 2008. DOI: 10.1016/j.jasms.2008.03.015.

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