A scalable workflow to characterize the human exposome.
Xin HuDouglas I WalkerYongliang LiangMatthew Ryan SmithMichael L OrrBrian D JuranChunyu MaKaran UppalC Michael HartGreg S MartinDavid C NeujahrCarmen J MarsitYoung-Mi GoKurt D PennellGary W MillerKonstantinos N LazaridisDean P JonesPublished in: Nature communications (2021)
Complementing the genome with an understanding of the human exposome is an important challenge for contemporary science and technology. Tens of thousands of chemicals are used in commerce, yet cost for targeted environmental chemical analysis limits surveillance to a few hundred known hazards. To overcome limitations which prevent scaling to thousands of chemicals, we develop a single-step express liquid extraction and gas chromatography high-resolution mass spectrometry analysis to operationalize the human exposome. We show that the workflow supports quantification of environmental chemicals in human plasma (200 µL) and tissue (≤100 mg) samples. The method also provides high resolution, sensitivity and selectivity for exposome epidemiology of mass spectral features without a priori knowledge of chemical identity. The simplicity of the method can facilitate harmonization of environmental biomonitoring between laboratories and enable population level human exposome research with limited sample volume.
Keyphrases
- endothelial cells
- gas chromatography
- high resolution mass spectrometry
- induced pluripotent stem cells
- public health
- pluripotent stem cells
- mass spectrometry
- healthcare
- magnetic resonance imaging
- liquid chromatography
- risk factors
- tandem mass spectrometry
- computed tomography
- drug delivery
- human health
- climate change
- electronic health record