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使用聚(N-异丙基丙烯酰胺)接枝硅胶的温度响应尺寸排阻色谱法。

Temperature-responsive size-exclusion chromatography using poly(N-isopropylacrylamide) grafted silica.

作者信息

Lakhiari H, Okano T, Nurdin N, Luthi C, Descouts P, Muller D, Jozefonvicz J

机构信息

Laboratoire de recherche sur les macromolécules, CNRS URA 502, Université Paris Nord, Institut Galilée, Villetaneuse, France.

出版信息

Biochim Biophys Acta. 1998 Mar 2;1379(3):303-13. doi: 10.1016/s0304-4165(97)00110-4.

Abstract

Silica-based packing materials induce non-specific interactions with proteins in aqueous media because of the nature of their surface, mainly silanol groups. Therefore, the silica surface has to be modified in order to be used as stationary phase for the High Performance Size-Exclusion Chromatography (HPSEC) of proteins. For this purpose, porous silica beads were coated with hydrophilic polymer gels (dextrans of different molecular weights) carrying a calculated amount of diethyl-aminoethyl groups (DEAE). Actually, as shown by HPSEC, these dextran modified supports minimize non-specific adsorption for proteins and pullulans in aqueous solution. Then, in order to change the pore size in response to temperature, temperature responsive polymer of poly(N-isopropylacrylamide) (PIPAAm) was introduced into the surface of dextran-DEAE on porous silica beads. The structure of these supports before and after modification was alternately studied by Scanning Electronic Microscopy (SEM) and Scanning Force Microscopy (SFM). An adsorption of radiolabelled albumin was performed to complete our study. Silica modifications by dextran-DEAE and PIPAAm improve the neutrality of the support and minimize the non-specific interactions between the solid support and proteins in solution. At low temperature, the support having PIPAAm exhibits a high resolution domain in HPSEC and finally permits a better resolution of proteins and pullulans. At higher temperature, hydrophobic properties of PIPAAm produce interactions with some proteins and trigger off a slight delay of their elution time.

摘要

基于硅胶的填充材料由于其表面性质(主要是硅醇基团),会在水性介质中与蛋白质产生非特异性相互作用。因此,为了用作蛋白质高效尺寸排阻色谱(HPSEC)的固定相,硅胶表面必须进行改性。为此,在多孔硅胶珠上涂覆了带有计算量二乙氨基乙基基团(DEAE)的亲水性聚合物凝胶(不同分子量的葡聚糖)。实际上,如HPSEC所示,这些葡聚糖改性的载体可最大程度减少水溶液中蛋白质和支链淀粉的非特异性吸附。然后,为了响应温度改变孔径,将聚(N-异丙基丙烯酰胺)(PIPAAm)的温度响应性聚合物引入多孔硅胶珠上葡聚糖-DEAE的表面。通过扫描电子显微镜(SEM)和扫描力显微镜(SFM)交替研究了这些载体改性前后的结构。进行放射性标记白蛋白的吸附以完成我们的研究。葡聚糖-DEAE和PIPAAm对硅胶的改性提高了载体的中性,并最大程度减少了固体载体与溶液中蛋白质之间的非特异性相互作用。在低温下,含有PIPAAm的载体在HPSEC中表现出高分辨率区域,最终能够更好地分离蛋白质和支链淀粉。在较高温度下,PIPAAm的疏水性会与一些蛋白质产生相互作用,并导致其洗脱时间略有延迟。

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