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通过形成取代亚胺酯而活化的尼龙上蛋白质的可逆固定化及其异常性质。

The reversible immobilization of proteins on nylon activated through the formation of a substituted imidoester, and its unusual properties.

作者信息

Sundaram P V

出版信息

Biochem J. 1979 Nov 1;183(2):445-51. doi: 10.1042/bj1830445.

Abstract

Alkylation of nylon produces nylon imidate, which is used for the covalent coupling of enzymes and other proteins and ligands. Nylon imidate is unusually stable when stored wet, with a half-life of about 60 days. Reaction with enzymes has an optimum about pH 7-8 and is extremely rapid, with about 60% of the reaction being complete in the first 10 min. The amidine formed in reaction with an amino group can be displaced by another nucleophile. In view of this finding that nylon amidine is capable of exchanging proteins, it is now concluded that nylon-tube reactors containing immobilized enzymes made by this method may not be used as extracorporeal shunts or as on-line monitors on patients, since the enzyme in the reactor may be released into the circulation by nucleophiles in the blood. This can lead to complications. The chemistry of this displacement reaction is discussed.

摘要

尼龙的烷基化会产生尼龙亚氨酸酯,它用于酶及其他蛋白质和配体的共价偶联。尼龙亚氨酸酯在湿态储存时异常稳定,半衰期约为60天。与酶的反应在pH约7 - 8时最适宜,且极其迅速,在前10分钟约60%的反应就能完成。与氨基反应形成的脒可被另一种亲核试剂取代。鉴于这一发现,即尼龙脒能够交换蛋白质,现在得出结论,由此方法制备的含有固定化酶的尼龙管反应器不能用作体外分流器或患者的在线监测器,因为反应器中的酶可能会被血液中的亲核试剂释放到循环系统中。这可能会导致并发症。本文讨论了这种取代反应的化学过程。

相似文献

7
Polysaccharide derivatives as coats for nylon tube urease.作为尼龙管脲酶包被物的多糖衍生物
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本文引用的文献

1
A Biochemically Specific Method for Enzyme Isolation.一种用于酶分离的生化特异性方法。
Proc Natl Acad Sci U S A. 1953 Apr;39(4):232-6. doi: 10.1073/pnas.39.4.232.
3
Some general methods of preparing affinity columns.制备亲和柱的一些常规方法。
Nucleic Acids Res. 1974 Nov;1(11):1587-99. doi: 10.1093/nar/1.11.1587.
4
Water-insoluble derivatives of enzymes, antigens, and antibodies.酶、抗原和抗体的水不溶性衍生物。
Annu Rev Biochem. 1966;35:873-908. doi: 10.1146/annurev.bi.35.070166.004301.
9
Formation of non-amidine products in the reaction of primary amines with imido esters.
Biochem Biophys Res Commun. 1975 Nov 3;67(1):126-32. doi: 10.1016/0006-291x(75)90292-2.

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