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DNA sequence analysis by hybridization with oligonucleotide microchips: MALDI mass spectrometry identification of 5mers contiguously stacked to microchip oligonucleotides

机译:通过与寡核苷酸微芯片杂交进行DNA序列分析:MALDI质谱鉴定连续堆叠到微芯片寡核苷酸的5mers

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摘要

Matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) has been applied to increase the informational output from DNA sequence analysis. It has been used to analyze DNA by hybridization with microarrays of gel-immobilized oligonucleotides extended with stacked 5mers. In model experiments, a 28 nt long DNA fragment was hybridized with 10 immobilized, overlapping 8mers. Then, in a second round of hybridization DNA–8mer duplexes were hybridized with a mixture of 10 5mers. The stability of the 5mer complex with DNA was increased to raise the melting temperature of the duplex by 10–15°C as a result of stacking interaction with 8mers. Contiguous 13 bp duplexes containing an internal break were formed. MALDI MS identified one or, in some cases, two 5mers contiguously stacked to each DNA–8mer duplex formed on the microchip. Incorporating a mass label into 5mers optimized MALDI MS monitoring. This procedure enabled us to reconstitute the sequence of a model DNA fragment and identify polymorphic nucleotides. The application of MALDI MS identification of contiguously stacked 5mers to increase the length of DNA for sequence analysis is discussed.
机译:基质辅助激光解吸电离质谱法(MALDI MS)已用于增加DNA序列分析的信息输出。它已通过与固定有堆叠5聚体的凝胶固定寡核苷酸微阵列杂交来分析DNA。在模型实验中,将28 nt长的DNA片段与10个固定的重叠8聚体杂交。然后,在第二轮杂交中,将DNA–8mer双链体与10个5mer的混合物杂交。 5mer复合物与DNA的稳定性提高了,由于与8mer的堆叠相互作用,双链体的解链温度提高了10-15°C。形成了包含内部断裂的连续的13 bp双链体。 MALDI MS鉴定了一个或在某些情况下两个5mer连续堆叠在微芯片上形成的每个DNA-8mer双链体上。将质量标签并入5mers优化的MALDI MS监测中。此过程使我们能够重构模型DNA片段的序列并鉴定多态性核苷酸。讨论了MALDI MS鉴定连续堆叠的5聚体以增加DNA长度以进行序列分析的应用。

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