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采用基质辅助激光解吸/电离飞行时间质谱法对载脂蛋白E进行基因分型。

Genotyping of apolipoprotein E by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

作者信息

Srinivasan J R, Kachman M T, Killeen A A, Akel N, Siemieniak D, Lubman D M

机构信息

Department of Chemistry, University of Michigan, Ann Arbor 48109, USA.

出版信息

Rapid Commun Mass Spectrom. 1998;12(16):1045-50. doi: 10.1002/(SICI)1097-0231(19980831)12:16<1045::AID-RCM281>3.0.CO;2-Y.

Abstract

The genotyping of the various isoforms of Apolipoprotein E (apo E) has been performed using matrix-assisted laser desorption/ionization (MALDI-MS). The polymerase chain reaction was used to amplify the specific apo E gene sequence followed by digestion with Cfo I (Clostridium formicoaceticum), for generating restriction fragments for rapid and accurate mass analysis. An exonuclease I digestion step was introduced to remove the unused primers after PCR, which can otherwise interfere in the mass spectral analysis. By replacing the gel electrophoresis detection step with MALDI-MS, restriction isotyping of the apo E gene was achieved. Genotyping of an unknown sample and obtained from an independent diagnostic laboratory demonstrated the validity of the MALDI-MS method for the routine analysis of apo E.

摘要

已使用基质辅助激光解吸/电离(MALDI-MS)对载脂蛋白E(apo E)的各种异构体进行基因分型。采用聚合酶链反应扩增特定的apo E基因序列,随后用甲酸乙酸梭菌(Cfo I)进行酶切,以产生用于快速准确质量分析的限制性片段。引入核酸外切酶I消化步骤以在PCR后去除未使用的引物,否则这些引物会干扰质谱分析。通过用MALDI-MS取代凝胶电泳检测步骤,实现了apo E基因的限制性分型。对来自独立诊断实验室的未知样品进行基因分型,证明了MALDI-MS方法用于apo E常规分析的有效性。

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