Stable Bioactive Enzyme-Containing Multi layer Films Based on Covalent Cross-Linking from Mussel-Inspired Adhesives

被引:15
作者
Longo, Johan [1 ]
Garnier, Tony [1 ]
Mateescu, Mihaela [2 ,3 ]
Ponzio, Florian [2 ,3 ]
Schaaf, Pierre [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Jierry, Loic [1 ,4 ,5 ,6 ]
Ball, Vincent [2 ,3 ]
机构
[1] Univ Strasbourg, Inst Charles Sadron, CNRS, UPR 22, F-67034 Strasbourg 2, France
[2] INSERM, Biomat & Bioingn, UMR S 1121, F-67085 Strasbourg, France
[3] Univ Strasbourg, Fac Chirurg Dent, F-67000 Strasbourg, France
[4] Univ Strasbourg, Ecole Chim Polymeres & Mat, F-67087 Strasbourg, France
[5] Univ Strasbourg, Inst Etud Avancees, F-67083 Strasbourg, France
[6] Int Ctr Frontier Res Chem, F-67083 Strasbourg, France
[7] Inst Univ France, F-75005 Paris, France
关键词
IMMOBILIZED ENZYMES; PROTEIN; MULTILAYERS; HYDROGELS; VESICLES; POLYMER; SURFACE;
D O I
10.1021/acs.langmuir.5b03329
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of immobilized enzymes is mandatory for the easy separation of the enzyme, the unreacted substrates, and the obtained products to allow repeated enzymatic assays without cumbersome purification steps. The immobilization procedure is however critical to obtain a high fraction of active enzyme. In this article, we present an enzyme immobilization strategy based on a catechol functionalized alginate. We demonstrate that alkaline phosphatase (ALP) remains active in multilayered films made with alginate modified with catechol moieties (AlgCat) for long duration, that is, up to 7 weeks, provided the multilayered architecture is crosslinked with sodium periodate. This cross-linking reaction allows to create covalent bonds between the amino groups of ALP and the quinone group carried by the modified alginate. In the absence of cross-linking, the enzymatic activity is rapidly lost and this reduction is mainly due to enzyme desorption. We also show that NaIO4 cross-linked (AlgCat-Alp)(n) films can be freeze-dried and reused at least 3 weeks later without lost in enzymatic activity.
引用
收藏
页码:12447 / 12454
页数:8
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