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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >FLUIDIFIED POLYACRYLAMIDES AS MOLECULAR SIEVES IN CAPILLARY ZONE ELECTROPHORESIS OF DNA FRAGMENTS
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FLUIDIFIED POLYACRYLAMIDES AS MOLECULAR SIEVES IN CAPILLARY ZONE ELECTROPHORESIS OF DNA FRAGMENTS

机译:DNA片段毛细管区带电泳中的分子筛流态化聚丙烯酰胺

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In order to optimize the separation of DNA fragments, in the 50-500 base pairs (bp) range, a typical size interval of most polymerase chain reaction-amplified DNA chains produced for analysis of genetic diseases, different ways of preparing liquid linear polyacrylamides were evaluated. Standard linear polyacrylamides (PAA), as prepared with typical levels of catalysts (1 mu l of pure N,N,N',N'-tetramethylethylenediamine and 4 mu l of 10% peroxodisulfate per mi of gelling solution) at room temperature, have extremely high weight-average molecular mass (M(w)) values (in excess of 2.10(6)) and can be injected or extruded from a capillary at concentrations above 6% only with great difficulty. The same polyacrylamide, if subjected to mastication by ultrasound at 45 kHz for up to ca. 50 h, exhibits much reduced viscosities (e.g. 700 vs. 3600 mPa s, at 8% concentration) and chain lengths (M(w) ca. 550000) and offers increased resolution in the 50-500 bp interval. However, chain rupture by ultrasound produces charged chains, which migrate out of the capillary under the influence of an electric field, thus impairing resolution. Two other ways have been found to produce uncharged, short chains of very low viscosity: chain termination in 2-propanol by polymerization at 35 and 70 degrees C, respectively. The latter process produces chains of M, as low as 230000 (M(n) = 55000; polydispersity = 4.2) with a viscosity of only 350 mPa s for a 10% polymer solution. In the separation of the seventeen DNA fragments of the marker pBR322/HaeIII (ranging in size from 51 to 587 bp), a 6% solution of ''short-chain polyacrylamide (PAA)'' affords a resolution of 880000 theoretical plates, vs. 440000 for ''long-chain PAA''. In a biological sample of a multiplex Duchenne muscular dystrophy containing eighteen DNA fragments, ''short-chain PAA'' resolves 17 of them, compared with a pattern of only eleven zones in ''long-chain PAA''. [References: 33]
机译:为了优化DNA片段的分离,在50-500个碱基对(bp)的范围内,这是大多数用于遗传病分析的聚合酶链反应扩增的DNA链的典型大小区间,采用了不同的制备液态线性聚丙烯酰胺的方法评估。标准的线性聚丙烯酰胺(PAA),在室温下用典型水平的催化剂(每毫升胶凝溶液中含1微升纯N,N,N',N'-四甲基乙二胺和4微升10%过氧二硫酸盐)制得,极高的重均分子量(M(w))值(超过2.10(6)),并且很难以高于6%的浓度从毛细管中注入或挤出。如果在45 kHz的频率下通过超声波进行咀嚼,则同一聚丙烯酰胺的最大寿命约为。 50 h时,粘度降低了很多(例如,浓度为8%时700 vs. 3600 mPa s)和链长(M(w)约为550000),并在50-500 bp的间隔内提供了更高的分辨率。但是,超声波导致的链断裂会产生带电链,这些带电链会在电场的影响下从毛细管中迁移出来,从而降低分离度。已经发现另外两种产生低电荷的不带电荷的短链的方法:分别在35和70摄氏度下通过聚合反应在2-丙醇中终止链。后一种方法产生的M链低至230000(M(n)= 55000;多分散度= 4.2),对于10%的聚合物溶液,其粘度仅为350 mPa s。在分离标记pBR322 / HaeIII的17个DNA片段(大小从51到587 bp)时,使用6%的“短链聚丙烯酰胺(PAA)”溶液可获得880000个理论塔板的分离度,而``长链PAA''为440000。在含有18个DNA片段的多重杜氏肌营养不良症的生物学样本中,“长链PAA”中只有11个区域,“短链PAA”可分辨其中的17个。 [参考:33]

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