Towards cracking the epigenetic code using a combination of high-throughput epigenomics and quantitative mass spectrometry-based proteomics

BioEssays ◽  
2011 ◽  
Vol 33 (7) ◽  
pp. 547-551 ◽  
Author(s):  
Hendrik G. Stunnenberg ◽  
Michiel Vermeulen
Molecules ◽  
2011 ◽  
Vol 16 (3) ◽  
pp. 2391-2413 ◽  
Author(s):  
Anne E. Boyer ◽  
Maribel Gallegos-Candela ◽  
Renato C. Lins ◽  
Zsuzsanna Kuklenyik ◽  
Adrian Woolfitt ◽  
...  

Author(s):  
Masaru Miyagi ◽  
Takhar Kasumov

The controlled and selective synthesis/clearance of biomolecules is critical for most cellular processes. In most high-throughput ‘omics’ studies, we measure the static quantities of only one class of biomolecules (e.g. DNA, mRNA, proteins or metabolites). It is, however, important to recognize that biological systems are highly dynamic in which biomolecules are continuously renewed and different classes of biomolecules interact and affect each other's production/clearance. Therefore, it is necessary to measure the turnover of diverse classes of biomolecules to understand the dynamic nature of biological systems. Herein, we explain why the kinetic analysis of a diverse range of biomolecules is important and how such an analysis can be done. We argue that heavy water ( 2 H 2 O) could be a universal tracer for monitoring the synthesis of biomolecules on a global scale. This article is part of the themed issue ‘Quantitative mass spectrometry’.


2007 ◽  
Vol 177 (4S) ◽  
pp. 52-53
Author(s):  
Stefano Ongarello ◽  
Eberhard Steiner ◽  
Regina Achleitner ◽  
Isabel Feuerstein ◽  
Birgit Stenzel ◽  
...  

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