Specific Detection of Cellular Glutamine Hydrolysis in Live Cells Using HNCO Triple Resonance NMR

Authors
Lee, SujinWen, HeCha, Jin WookPark, Sunghyouk
Issue Date
2016-11
Publisher
AMER CHEMICAL SOC
Citation
ACS CHEMICAL BIOLOGY, v.11, no.11, pp.3140 - 3145
Abstract
Glutamine plays key roles as a biosynthetic precursor or an energy source in cancers, and interest in its metabolism is rapidly growing. However, the proper evaluation of glutamine hydrolysis, the very first reaction in the entire glutaminolysis, has been difficult. Here, we report a triple resonance NMR-based assay for specific detection of glutaminase activity carrying out this reaction using stable-isotope labeled glutamine. Compared to conventional methods involving coupled enzyme assays, the proposed approach is direct because it detects the presence of the H-N-CO amide spin system. In addition, the method is unique in enabling the measurement of glutamine hydrolysis reaction in real-time in live cells. The approach was applied to investigating the effects of a glutaminase inhibitor and the inhibitory effects of glucose on glutamine metabolism in live cells. It can be easily applied to studying other signals that affect cellular glutamine metabolism.
Keywords
PHOSPHATE-DEPENDENT GLUTAMINASE; CANCER METABOLISM; ASSAY; EXPRESSION; DEHYDROGENASE; ASPARAGINASE; MITOCHONDRIA; SUPPRESSION; INHIBITION; GLUCOSE; PHOSPHATE-DEPENDENT GLUTAMINASE; CANCER METABOLISM; ASSAY; EXPRESSION; DEHYDROGENASE; ASPARAGINASE; MITOCHONDRIA; SUPPRESSION; INHIBITION; GLUCOSE
ISSN
1554-8929
URI
https://pubs.kist.re.kr/handle/201004/123489
DOI
10.1021/acschembio.6b00493
Appears in Collections:
KIST Article > 2016
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE