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Lack of Evidence for PKM2 Protein Kinase Activity
被引:90
|作者:
Hosios, Aaron M.
[1
]
Fiske, Brian P.
[1
]
Gui, Dan Y.
[1
]
Vander Heiden, Matthew G.
[1
,2
]
机构:
[1] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
关键词:
PYRUVATE-KINASE;
GENE-TRANSCRIPTION;
M2;
PHOSPHORYLATION;
ISOFORM;
PROMOTES;
SERINE;
TYROSINE;
ATP;
D O I:
10.1016/j.molcel.2015.07.013
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The role of pyruvate kinase M2 (PKM2) in cell proliferation is controversial. A unique function of PKM2 proposed to be important for the proliferation of some cancer cells involves the direct activity of this enzyme as a protein kinase; however, a detailed biochemical characterization of this activity is lacking. Using [P-32]-phosphoenolpyruvate (PEP) we examine the direct substrates of PKM2 using recombinant enzyme and in vitro systems where PKM2 is genetically deleted. Labeling of some protein species from [P-32]-PEP can be observed; however, most were dependent on the presence of ADP, and none were dependent on the presence of PKM2. In addition, we also failed to observe PKM2-dependent transfer of phosphate from ATP directly to protein. These findings argue against a role for PKM2 as a protein kinase.
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页码:850 / 857
页数:8
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