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首页> 外文期刊>Journal of inherited metabolic disease >Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders.
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Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders.

机译:通过串联质谱直接多重分析干血斑中的酶,用于新生儿筛查溶酶体贮积病。

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Tandem mass spectrometry is currently used in newborn screening programmes to quantify the level of amino acids and acylcarnitines in dried blood spots for detection of metabolites associated with treatable diseases. We have developed assays for lysosomal enzymes in rehydrated dried blood spots in which a set of substrates is added and the set of corresponding enzymatic products are quantified using tandem mass spectrometry with the aid of mass-differentiated internal standards. We have developed a multiplex assay of the set of enzymes that, when deficient, cause the lysosomal storage disorders Fabry, Gaucher, Hurler, Krabbe, Niemann-Pick A/B and Pompe diseases. These diseases were selected because treatments are now available or expected to emerge shortly. The discovery that acarbose is a selective inhibitor of maltase glucoamylase allows the Pompe disease enzyme, acid alpha-glucosidase, to be selectively assayed in white blood cells and dried blood spots. When tested with dried blood spots from 40 unaffected individuals and 10-12 individuals with the lysosomal storage disorder, the tandem mass spectrometry assay led to the correct identification of the affected individuals with 100% sensitivity. Many of the reagents needed for the new assays are commercially available, and those that are not are being prepared under Good Manufacturing Procedures for approval by the FDA. Our newborn screening assay for Krabbe disease is currently being put in place at the Wadsworth Center in New York State for the analysis of approximately 1000 dried blood spots per day. Summary We have developed tandem mass spectrometry for the direct assay of lysosomal enzymes in rehydrated dried blood spots that can be implemented for newborn screening of lysosomal storage disorders. Several enzymes can be analysed by a single method (multiplex analysis) and in a high-throughput manner appropriate for newborn screening laboratories.
机译:串联质谱法目前用于新生儿筛查程序中,以定量检测干血斑中氨基酸和酰基肉碱的水平,以检测与可治疗疾病相关的代谢物。我们已经开发了复水后的干燥血斑中溶酶体酶的检测方法,其中添加了一组底物,并使用串联质谱在质量差异内标的帮助下对了一组相应的酶产物进行了定量。我们已经开发了一套酶的多重分析方法,这些酶在缺乏时会引起溶酶体贮积病,法布里,高雪,霍勒,克拉贝,尼曼-皮克A / B和庞贝病。选择这些疾病是因为现在可以使用治疗方法,或者预计很快就会出现治疗方法。阿卡波糖是麦芽糖酶葡糖淀粉酶的选择性抑制剂的发现使庞贝病酶酸性α-葡糖苷酶能够在白细胞和干血斑中进行选择性测定。用来自40个未受影响的个体和10-12个患有溶酶体贮积症的个体的干血斑进行测试时,串联质谱分析法以100%的敏感性正确鉴定了受影响的个体。新测定法所需的许多试剂可商购,而那些未按照良好生产程序制备且需​​要FDA批准的试剂。我们目前正在纽约州的沃兹沃思中心进行我们针对Krabbe病的新生儿筛查试验,每天分析约1000个干血斑。总结我们已经开发了串联质谱法,用于直接测定复水的干血斑中的溶酶体酶,可用于新生儿筛查溶酶体贮积病。几种酶可以通过一种方法(多重分析)以适合新生儿筛查实验室的高通量方式进行分析。

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