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.
引用
收藏
页码:850 / 857
页数:8
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