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使用聚乙烯吡咯烷酮和聚(N,N-二甲基丙烯酰胺)瞬态互穿网络通过毛细管电泳分离双链DNA片段。

Separation of double-stranded DNA fragments by capillary electrophoresis using polyvinylpyrrolidone and poly(N,N-dimethylacrylamide) transient interpenetrating network.

作者信息

Wang Yanmei, Liang Dehai, Hao Jingcheng, Fang Dufei, Chu Benjamin

机构信息

Chemistry Department, State University of New York at Stony Brook, Stony Brook, NY 11794-3400, USA.

出版信息

Electrophoresis. 2002 May;23(10):1460-6. doi: 10.1002/1522-2683(200205)23:10<1460::AID-ELPS1460>3.0.CO;2-J.

Abstract

A noncross-linked interpenetrating polymer network (IPN), consisting of poly(N,N-dimethylacrylamide) (PDMA) and polyvinylpyrrolidone (PVP, weight-average molecular weight M(w) = 1 x 10(6) g/mol) was synthesized by polymerizing N,N-dimethylacrylamide (DMA) monomers directly in PVP buffer solution and tested as a separation medium for double-stranded (ds)DNA analysis without further purification. Due to the incompatibility of PVP and PDMA, a simple solution mixture could incur a microphase separation and showed poor performance on dsDNA separation. However, a dramatic improvement was achieved by the formation of an IPN. We attributed the high sieving ability of IPN as due to an increase in the number of entanglements by the more extended polymer chains. Apparent viscosity studies showed that the IPN had a much higher viscosity than the simple mixture containing the same amount of PDMA and PVP. In 1 x Tris-borate-EDTA (TBE) buffer, the concentration ratio of PDMA and PVP had a great effect on the DNA separation. At optimal conditions, the 22 fragments in pBR322/HaeIII DNA were successfully separated within 15 min, with a resolution of better than 1.0 for 123/124 bp.

摘要

通过在聚乙烯吡咯烷酮(PVP,重均分子量M(w)=1×10(6) g/mol)缓冲溶液中直接聚合N,N-二甲基丙烯酰胺(DMA)单体,合成了一种由聚(N,N-二甲基丙烯酰胺)(PDMA)和聚乙烯吡咯烷酮组成的非交联互穿聚合物网络(IPN),并将其作为双链(ds)DNA分析的分离介质进行测试,无需进一步纯化。由于PVP和PDMA不相容,简单的溶液混合物会发生微相分离,并且在dsDNA分离方面表现不佳。然而,通过形成IPN实现了显著的改善。我们将IPN的高筛分能力归因于聚合物链更加伸展导致缠结数量增加。表观粘度研究表明,IPN的粘度比含有相同量PDMA和PVP的简单混合物高得多。在1×Tris-硼酸-乙二胺四乙酸(TBE)缓冲液中,PDMA和PVP的浓度比对DNA分离有很大影响。在最佳条件下,pBR322/HaeIII DNA中的22个片段在15分钟内成功分离,123/124 bp的分辨率优于1.0。

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