Onaizi Sagheer A
Department of Chemical Engineering, King Fahd University of Petroleum and Minerals, Dhahran, 31216, Saudi Arabia.
Eur Biophys J. 2018 Dec;47(8):951-960. doi: 10.1007/s00249-018-1320-4. Epub 2018 Jul 9.
Protein fouling is a serious problem in many food, pharmaceutical and household industries. In this work, the removal of rubisco protein fouling from cellulosic surfaces using a protease (subtilisin A) has been investigated experimentally and mathematically. The cellulosic surfaces were prepared using self-assembled monolayers (SAMs) on a surface plasmon resonance biosensor (chip) surface after conjugating cellulose to α-lipoic acid. Rubisco adsorption on the prepared cellulosic SAMs was found to be irreversible, leading to the creation of a tough protein fouling. The heterogeneous enzymatic cleansing of such tough fouling involves enzyme transfer to the surface and the subsequent removal of the rubisco via protease activity. In this work, these two processes were decoupled, allowing enzyme transfer and enzymatic surface reaction to be parameterized separately. Mathematical modeling of the enzymatic cleaning of protein fouling from cellulosic SAMs revealed that enzymatic mobility at the interface is an important factor. The approach presented in this work might be useful in designing better protein fouling-resistant surfaces. It could also be used to guide efforts to screen and gauge the cleaning performance of detergent-enzyme formulations.
蛋白质污垢是许多食品、制药和家用行业中存在的严重问题。在这项工作中,已通过实验和数学方法研究了使用蛋白酶(枯草杆菌蛋白酶A)从纤维素表面去除核酮糖-1,5-二磷酸羧化酶/加氧酶(rubisco)蛋白质污垢的情况。在将纤维素与α-硫辛酸共轭后,利用自组装单分子层(SAMs)在表面等离子体共振生物传感器(芯片)表面制备纤维素表面。发现rubisco在制备的纤维素SAMs上的吸附是不可逆的,从而导致形成顽固的蛋白质污垢。对这种顽固污垢的非均相酶促清洁涉及酶向表面的转移以及随后通过蛋白酶活性去除rubisco。在这项工作中,将这两个过程解耦,使得酶转移和酶促表面反应能够分别进行参数化。对从纤维素SAMs上去除蛋白质污垢的酶促清洁过程进行数学建模表明,界面处的酶迁移率是一个重要因素。这项工作中提出的方法可能有助于设计出更好的抗蛋白质污垢表面。它还可用于指导筛选和评估洗涤剂-酶配方清洁性能的工作。