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用加速器质谱法定量同位素分子标记物。

Quantitating isotopic molecular labels with accelerator mass spectrometry.

作者信息

Vogel John S, Love Adam H

机构信息

Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, Livermore, California, USA.

出版信息

Methods Enzymol. 2005;402:402-22. doi: 10.1016/S0076-6879(05)02013-6.

Abstract

Accelerator mass spectrometry (AMS) traces isotopically labeled biochemicals and provides significant new directions for understanding molecular kinetics and dynamics in biological systems. AMS traces low-abundance radioisotopes for high specificity but detects them with MS for high sensitivity. AMS reduces radiation exposure doses to levels safe for use in human volunteers of all ages. Total radiation exposures are equivalent to those obtained in very short airplane flights, a commonly accepted radiation risk. Waste products seldom reach the Nuclear Regulatory Commission (NRC) definition of radioactive waste material for (14)C and (3)H. Attomoles of labeled compounds are quantified in milligram-sized samples, such as 20 microl of blood. AMS is available from several facilities that offer services and new spectrometers that are affordable. Detailed examples of designing AMS studies are provided, and the methods of analyzing AMS data are outlined.

摘要

加速器质谱法(AMS)可追踪同位素标记的生物化学物质,并为理解生物系统中的分子动力学和动态变化提供重要的新方向。AMS追踪低丰度放射性同位素以实现高特异性,但通过质谱仪检测它们以实现高灵敏度。AMS将辐射暴露剂量降低到对所有年龄段的人类志愿者都安全的水平。总辐射暴露量相当于在非常短的飞机飞行中所获得的暴露量,这是一种普遍接受的辐射风险。对于碳-14(¹⁴C)和氢-3(³H),其废弃物很少达到美国核管理委员会(NRC)对放射性废料的定义。在毫克级样本(如20微升血液)中可对阿托摩尔级的标记化合物进行定量分析。有几家机构提供AMS服务,还有价格实惠的新型光谱仪可供使用。文中提供了设计AMS研究的详细示例,并概述了分析AMS数据的方法。

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