色谱 ›› 2020, Vol. 38 ›› Issue (9): 1022-1027.DOI: 10.3724/SP.J.1123.2020.02028

• 专论与综述 • 上一篇    下一篇

聚(2-甲基-2-噁唑啉)在毛细管电泳分离蛋白质中的应用

王雨晨, 王延梅()   

  1. 中国科学技术大学高分子科学与工程系, 安徽 合肥 230026
  • 收稿日期:2020-02-28 出版日期:2020-09-08 发布日期:2020-12-11
  • 通讯作者: 王延梅
  • 作者简介:王延梅.Tel:(0551)63607652, E-mail:wangyanm@ustc.edu.cn
  • 基金资助:
    国家自然科学基金项目(21674102);国家自然科学基金项目(21374109)

Application of poly(2-methyl-2-oxazoline) in protein separation by capillary electrophoresis

WANG Yuchen, WANG Yanmei()   

  1. Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, China
  • Received:2020-02-28 Online:2020-09-08 Published:2020-12-11
  • Contact: WANG Yanmei
  • Supported by:
    National Natural Science Foundation of China(21674102);National Natural Science Foundation of China(21374109)

摘要:

毛细管电泳作为一种常见的液相分离技术,因其分析速度快、分离效率高、样品消耗量少等特点,在蛋白质分离分析领域有广泛应用。然而,常用的熔融硅毛细管容易吸附蛋白质,导致电渗流不稳定,分离结果重现性变差;此外,商用毛细管电泳中常用的紫外检测器由于光程短,使得毛细管电泳的检测灵敏度往往不能达到低丰度蛋白质的直接分析要求。因此寻找能够阻止蛋白质吸附、同时能够提高检测灵敏度的涂层是毛细管电泳分离分析蛋白质的重要课题之一。聚(2-甲基-2-噁唑啉)(PMOXA)作为一种类肽类亲水性聚合物,具有与抗蛋白质吸附聚合物聚乙二醇类似的亲水性、抗蛋白质吸附性和生物相容性,而且其类肽结构使之具有较聚乙二醇更好的稳定性,因此近年来在生物质传递、药物载体和阻抗蛋白质吸附等领域得到越来越多的应用。该文主要从两个方面对聚(2-甲基-2-噁唑啉)在毛细管电泳中的应用进行了阐述。一是利用多巴胺作为黏合层将其涂覆在毛细管内壁作为抗蛋白质吸附涂层,这种涂层不仅能成功分离多种蛋白质的混合物(如溶菌酶、细胞色素C、核糖核酸酶A和α-胰凝乳蛋白酶原A),而且在定量检测奶粉中三聚氰胺、乳铁蛋白的过程中,能阻抗其他蛋白质的非特异性吸附,提高了毛细管电泳对奶粉中三聚氰胺、乳铁蛋白的检测效率。二是将其与具有刺激响应性的聚合物(如聚丙烯酸)构成二元混合刷涂层,在一定的pH和离子强度条件下,涂层可吸附目标蛋白质(如牛血清白蛋白、溶菌酶),在另一pH和离子强度条件下可将吸附的目标蛋白质全部释放,同时在释放过程中,处于涂层表面的聚(2-甲基-2-噁唑啉)会进一步阻止蛋白质的吸附,释放的蛋白质在电渗流和电泳的双重作用下快速迁移,到达检测器的蛋白质瞬时浓度大大增加,使目标蛋白质得到富集,目标蛋白质的检测信号得到放大,从而达到了提高低丰度蛋白质检测灵敏度的目的。此外,该文还对聚(2-甲基-2-噁唑啉)在毛细管电泳分离蛋白质中的未来发展趋势进行了展望。

关键词: 毛细管电泳, 抗蛋白质吸附, 蛋白质分离, 在线富集, 聚(2-甲基-2-噁唑啉), 综述

Abstract:

Capillary electrophoresis (CE), a commonly used liquid-phase separation technology, has many advantages such as high analysis speed, high separation efficiency, and low sample consumption. Hence, CE has gained popularity in food analysis, medical clinical diagnosis, environmental monitoring, and biological sample separation, especially in the field of protein separation and analysis. However, the fused silica capillaries that are commonly used in CE easily adsorb proteins, resulting in unstable electroosmotic flow and poor reproducibility of the separation results. In addition, due to the short optical path of the typical ultraviolet detectors employed in commercial CE, the detection sensitivity often does not meet the requirements for the direct analysis of low-abundance proteins. Therefore, developing a coating that can prevent protein adsorption and improve detection sensitivity is one of the important challenges in CE separation and analysis of proteins. Poly(2-methyl-2-oxazoline), a peptide-like hydrophilic polymer, not only has hydrophilicity, protein-repellent ability, and biocompatibility similar to the gold standard of the anti-protein adsorption polymer (polyethylene glycol), but also shows better stability than polyethylene glycol due to its peptide-like structure. Therefore, it has been increasingly used in biomass transfer, drug carrier, and impedance protein adsorption in recent years. This article aims to review the recent applications of poly(2-methyl-2-oxazoline) in CE from two standpoints. First, poly(2-methyl-2-oxazoline) was grafted onto the capillary inner wall using polydopamine as an anchor. The resulting coated capillary successfully separated a mixture of proteins (such as lysozyme, cytochrome C, ribonuclease A, and α -pancreas chymosinogen A), in addition to preventing the non-specific adsorption of other proteins during the quantitative analysis of melamine and lactoferrin in milk powder. Thus, the detection efficiency of melamine and lactoferrin in milk powder was improved. Second, poly(2-methyl-2-oxazoline) was used to produce a binary mixed brush coating with a stimulus-responsive polymer (such as polyacrylic acid). The capillary coated with the mixed brushes could adsorb high amounts of the target protein (such as bovine serum albumin and lysozyme) under certain pH and ionic strength conditions, and most of the adsorbed proteins could be desorbed by changing the pH and ionic strength. During the release, poly(2-methyl-2-oxazoline) present on the coating would prevent the adsorption of proteins. Under the dual effects of electroosmotic flow and electrophoresis, the released protein could migrate rapidly, and the instantaneous concentration of the protein reaching the detector could be greatly increased. Therefore, the target proteins could be on-line concentrated and the detection signals could be amplified, resulting in improved detection sensitivity for the protein. Future development trends in the function of poly(2-methyl-2-oxazoline) for the separation of proteins by CE are also discussed.

Key words: capillary electrophoresis (CE), anti-protein adsorption, protein separation, on-line preconcentration, poly(2-methyl-2-oxazoline) (PMOXA), review