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本文引用的文献

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Monitoring the inflammatory response to infection through the integration of MALDI IMS and MRI.通过 MALDI IMS 和 MRI 的整合来监测感染的炎症反应。
Cell Host Microbe. 2012 Jun 14;11(6):664-73. doi: 10.1016/j.chom.2012.04.018.
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Structure, function and diversity of the healthy human microbiome.健康人体微生物组的结构、功能与多样性。
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Mass spectral molecular networking of living microbial colonies.微生物菌落的质谱分子网络分析。
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Innovation: Metabolomics: the apogee of the omics trilogy.创新:代谢组学:组学三部曲的巅峰。
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Targeted data extraction of the MS/MS spectra generated by data-independent acquisition: a new concept for consistent and accurate proteome analysis.靶向提取数据独立采集产生的 MS/MS 谱图:一致且准确的蛋白质组分析的新概念。
Mol Cell Proteomics. 2012 Jun;11(6):O111.016717. doi: 10.1074/mcp.O111.016717. Epub 2012 Jan 18.
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Bacteroides in the infant gut consume milk oligosaccharides via mucus-utilization pathways.婴儿肠道中的拟杆菌通过黏液利用途径消耗乳寡糖。
Cell Host Microbe. 2011 Nov 17;10(5):507-14. doi: 10.1016/j.chom.2011.10.007. Epub 2011 Oct 27.
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Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease.肠道菌群对磷脂酰胆碱的代谢作用促进了心血管疾病的发生。
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MALDI imaging mass spectrometry of human tissue: method challenges and clinical perspectives.基质辅助激光解吸电离成像质谱技术在人体组织中的应用:方法挑战与临床前景。
Trends Biotechnol. 2011 Mar;29(3):136-43. doi: 10.1016/j.tibtech.2010.12.002. Epub 2011 Feb 2.
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Bifidobacteria can protect from enteropathogenic infection through production of acetate.双歧杆菌可以通过产生乙酸盐来预防肠致病性感染。
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利用成像质谱和纳喷雾电喷雾离子化技术对模型肠道微生物组进行分子分析揭示了饮食代谢产物的转化。

Molecular analysis of model gut microbiotas by imaging mass spectrometry and nanodesorption electrospray ionization reveals dietary metabolite transformations.

机构信息

Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, San Diego, California 92093, United States.

出版信息

Anal Chem. 2012 Nov 6;84(21):9259-67. doi: 10.1021/ac302039u. Epub 2012 Oct 10.

DOI:10.1021/ac302039u
PMID:23009651
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3711173/
Abstract

The communities constituting our microbiotas are emerging as mediators of the health-disease continuum. However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial species within the gastrointestinal (GI) tract. Herein, we apply imaging mass spectrometry (IMS) to localize metabolites from the interaction between the host and colonizing microbiota. This approach complements other molecular imaging methodologies in that analytes need not be known a priori, offering the possibility of untargeted analysis. Localized molecules within the GI tract were then identified in situ by surface sampling with nanodesorption electrospray ionization Fourier transform ion cyclotron resonance-mass spectrometry (nanoDESI FTICR-MS). Products from diverse structural classes were identified including cholesterol-derived lipids, glycans, and polar metabolites. Specific chemical transformations performed by the microbiota were validated with bacteria in culture. This study illustrates how untargeted spatial characterization of metabolites can be applied to the molecular dissection of complex biology in situ.

摘要

构成我们微生物组的群落正在成为健康-疾病连续体的介导者。然而,由于胃肠道 (GI) 道内化学物质和微生物种类的不均匀分布,破译微生物群落对宿主病理生理学的功能影响是一项艰巨的挑战。在这里,我们应用成像质谱 (IMS) 来定位宿主与定植微生物群相互作用产生的代谢物。这种方法补充了其他分子成像方法,因为分析物不需要事先知道,从而提供了非靶向分析的可能性。然后通过纳米解吸电喷雾电离傅里叶变换离子回旋共振-质谱 (nanoDESI FTICR-MS) 对胃肠道内的局部分子进行表面采样原位鉴定。鉴定出了包括胆固醇衍生脂质、聚糖和极性代谢物在内的多种结构类别的产物。通过培养中的细菌验证了微生物群进行的特定化学转化。本研究说明了如何将代谢物的非靶向空间特征应用于原位复杂生物学的分子剖析。