Temporini Caterina, Calleri Enrica, Campèse Daniel, Cabrera Karin, Félix Guy, Massolini Gabriella
Department of Pharmaceutical Chemistry, University of Pavia, Pavia, Italy.
J Sep Sci. 2007 Nov;30(17):3069-76. doi: 10.1002/jssc.200700337.
The preparation and optimization of a new monolithic chymotrypsin bioreactor for online protein digestion is described. Silica monolithic supports have been activated with epoxide functionalities following an optimized in situ procedure and used for covalent immobilization of chymotrypsin in one-step reaction under different conditions. A total of four bioreactors were prepared and characterized in terms of the amount of immobilized enzyme and apparent active units by using a standard substrate, N-benzoyl-L-tyrosine p-nitroanilide (BTPNA). The stability of the bioreactors was evaluated and the morphology of the support after immobilization and use was studied by SEM analysis. The proteolytic activity of the optimized chymotrypsin bioreactor was evaluated using HSA as a model protein by online coupling of the bioreactor with LC-ESI-MS. With the online protocol, complete protein digestion in 120 min was achieved with a sequence coverage of 97.3%.
本文描述了一种用于在线蛋白质消化的新型整体式胰凝乳蛋白酶生物反应器的制备及优化。二氧化硅整体式载体已按照优化的原位程序用环氧化官能团进行活化,并用于在不同条件下通过一步反应共价固定胰凝乳蛋白酶。共制备了四个生物反应器,并通过使用标准底物N-苯甲酰-L-酪氨酸对硝基苯胺(BTPNA),根据固定化酶的量和表观活性单位进行了表征。评估了生物反应器的稳定性,并通过扫描电子显微镜(SEM)分析研究了固定化和使用后载体的形态。通过将生物反应器与液相色谱-电喷雾电离质谱(LC-ESI-MS)在线联用,以人血清白蛋白(HSA)作为模型蛋白评估了优化后的胰凝乳蛋白酶生物反应器的蛋白水解活性。采用在线方案,在120分钟内实现了蛋白质的完全消化,序列覆盖率为97.3%。