Lin Shuang, Yao Guoping, Qi Dawei, Li Yan, Deng Chunhui, Yang Pengyuan, Zhang Xiangmin
Department of Chemistry & Institute of Biomedical Sciences, Fudan University, Shanghai 200433, China.
Anal Chem. 2008 May 15;80(10):3655-65. doi: 10.1021/ac800023r. Epub 2008 Apr 11.
A fast and efficient proteolysis approach of microwave-assisted protein digestion was developed by using trypsin-immobilized magnetic silica (MS) microspheres. In the work, immobilization of the enzyme onto MS microspheres was very simple and only through a one-step reaction with 3-glycidoxypropyltrimethoxysilane (GLYMO) which provides the epoxy group as a reactive spacer. Considering that the magnetic particles are excellent microwave absorbers, we developed a novel microwave-assisted digestion method based on the easily prepared trypsin-immobilized MS microspheres. This novel digestion method combined the advantages of immobilized trypsin and the rapid-fashion of microwave-assisted digestion, which resulted in high digestion efficiency. BSA and myoglobin were used as model proteins to optimize the conditions of this method. Peptide fragments produced in 15 s could be confidently identified by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) analysis. Equivalent or better digestion efficiency was observed comparing to current in-solution digestion. Besides, because of the unique magnetic responsivity, the immobilized trypsin can be isolated easily with the help of an external magnet and thus used repeatedly. High activity was obtained even after seven runs of the trypsin-immobilized MS microspheres. To further verify its efficiency in proteome analysis, one reversed-phase liquid chromatography (RPLC) fraction of rat liver extract was applied. After 15 s incubation, 16 totally unique peptides corresponding to two proteins were identified. Finally, the rat liver sample was used to evaluate its worth for the application. With analysis by liquid chromatography-electrospray-tandem mass spectrometry (LC-ESI-MS/MS), comparable digestion efficiency was observed with typical in-solution digestion but the incubation time was largely shortened. This new microwave-assisted digestion method will hasten the application of the proteome technique to biomedical and clinical research.
通过使用固定化胰蛋白酶的磁性二氧化硅(MS)微球,开发了一种快速高效的微波辅助蛋白质消化的蛋白水解方法。在这项工作中,将酶固定在MS微球上非常简单,只需通过与3-缩水甘油氧基丙基三甲氧基硅烷(GLYMO)进行一步反应,GLYMO提供环氧基团作为反应间隔基。考虑到磁性颗粒是优异的微波吸收剂,我们基于易于制备的固定化胰蛋白酶的MS微球开发了一种新型的微波辅助消化方法。这种新型消化方法结合了固定化胰蛋白酶的优点和微波辅助消化的快速特性,从而实现了高消化效率。使用牛血清白蛋白(BSA)和肌红蛋白作为模型蛋白来优化该方法的条件。通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)分析,可以可靠地鉴定在15秒内产生的肽片段。与当前的溶液内消化相比,观察到了相当或更好的消化效率。此外,由于独特的磁响应性,固定化胰蛋白酶可以在外部磁铁的帮助下轻松分离,从而可以重复使用。即使经过七次使用固定化胰蛋白酶的MS微球后,仍能获得高活性。为了进一步验证其在蛋白质组分析中的效率,应用了大鼠肝脏提取物的一个反相液相色谱(RPLC)馏分。经过15秒的孵育,鉴定出了对应于两种蛋白质的16个完全独特的肽段。最后,使用大鼠肝脏样品评估其应用价值。通过液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)分析,观察到与典型的溶液内消化相当的消化效率,但孵育时间大大缩短。这种新的微波辅助消化方法将加速蛋白质组技术在生物医学和临床研究中的应用。