Kan Cheuk-Wai, Doherty Erin A S, Barron Annelise E
Department of Chemical Engineering, Northwestern University, Evanston, IL 60208, USA.
Electrophoresis. 2003 Dec;24(24):4161-9. doi: 10.1002/elps.200305670.
We have developed a novel class of thermogelling polymer networks based on poly-N-alkoxyalkylacrylamides, and demonstrated their use as DNA sequencing matrices for high-throughput microchannel electrophoresis in capillary arrays. Polymers and copolymers of N-ethoxyethylacrylamide (NEEA) and N-methoxyethylacrylamide (NMEA) were synthesized by aqueous-phase free-radical polymerization and characterized by tandem gel permeation chromatography-multi-angle laser light scattering. These copolymer matrices exhibit "re-entrant"-type volume phase transitions, forming entangled networks with high shear viscosity at low (< 20 degrees C) and high (> 35 degrees C) temperatures, and undergoing a "coil-to-globular", lower critical solution temperature (LCST)-like phase transition over an intermediate temperature range (20-35 degrees C). Hence, matrix viscosity is relatively low at room temperature (25 degrees C), and increases rapidly above 35 degrees C. The material properties and phase behavior of these thermogelling polymer networks were studied by steady-shear rheometry. These matrices are easily loaded into capillary arrays at room temperature while existing as viscous fluids, but thermogel above 35 degrees C to form transparent hydrogels via a thermo-associative phase transition. The extent of the intermediate viscosity drop and the final viscosity increase depends on the composition of the copolymers. DNA sequencing by capillary array electrophoresis with four-color laser-induced fluorescence (LIF) detection shows that these thermogelling networks provide enhanced resolution of both small and large DNA sequencing fragments and longer sequencing read lengths, in comparison to appropriate control (closely related, nonthermogelling) polymer networks. In particular, a copolymer comprised of 90% w/w NMEA and 10% w/w NEEA, with a molecular mass of approximately 2 MDa, delivers around 600 bases at 98.5% base-calling accuracy in 100 min of electrophoresis.
我们基于聚-N-烷氧基烷基丙烯酰胺开发了一类新型的热凝胶聚合物网络,并证明了它们作为DNA测序基质在毛细管阵列中的高通量微通道电泳中的应用。通过水相自由基聚合合成了N-乙氧基乙基丙烯酰胺(NEEA)和N-甲氧基乙基丙烯酰胺(NMEA)的聚合物和共聚物,并通过串联凝胶渗透色谱-多角度激光光散射进行了表征。这些共聚物基质表现出“折返”型体积相变,在低温(<20℃)和高温(>35℃)下形成具有高剪切粘度的缠结网络,并在中间温度范围(20-35℃)经历“线圈到球状”的、类似低临界溶液温度(LCST)的相变。因此,基质粘度在室温(25℃)下相对较低,在35℃以上迅速增加。通过稳态剪切流变学研究了这些热凝胶聚合物网络的材料性能和相行为。这些基质在室温下作为粘性流体时很容易加载到毛细管阵列中,但在35℃以上会热凝胶化,通过热缔合相变形成透明水凝胶。中间粘度下降和最终粘度增加的程度取决于共聚物的组成。与合适的对照(密切相关的、非热凝胶化)聚合物网络相比,通过毛细管阵列电泳结合四色激光诱导荧光(LIF)检测进行的DNA测序表明,这些热凝胶网络提高了小DNA和大DNA测序片段的分辨率以及更长的测序读长。特别是,一种由90% w/w NMEA和10% w/w NEEA组成、分子量约为2 MDa的共聚物,在100分钟的电泳中以98.5%的碱基识别准确率提供约600个碱基的测序结果。