Quantitative imaging of subcellular metabolism with stable isotopes and multi-isotope imaging mass spectrometry

被引:41
作者
Steinhauser, Matthew L. [1 ,2 ,3 ,4 ]
Lechene, Claude P. [1 ,2 ,3 ,5 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Genet, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA 02115 USA
[5] Natl Resource Imaging Mass Spectrometry, Cambridge, MA 02139 USA
关键词
Stable isotope; Quantitative imaging; Stem cell; Human; Metabolism; Cell division; NITROGEN-FIXATION; DNA; CELLS; CARBON; SEGREGATION; TURNOVER; DIVISION; RENEWAL; STRANDS; RATES;
D O I
10.1016/j.semcdb.2013.05.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multi-isotope imaging mass spectrometry (MIMS) is the quantitative imaging of stable isotope labels in cells with a new type of secondary ion mass spectrometer (NanoSIMS). The power of the methodology is attributable to (i) the immense advantage of using non-toxic stable isotope labels, (ii) high resolution imaging that approaches the resolution of usual transmission electron microscopy and (iii) the precise quantification of label down to 1 part-per-million and spanning several orders of magnitude. Here we review the basic elements of MIMS and describe new applications of MIMS to the quantitative study of metabolic processes including protein and nucleic acid synthesis in model organisms ranging from microbes to humans. (C) 2013 Published by Elsevier Ltd.
引用
收藏
页码:661 / 667
页数:7
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