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Kinetics of Phosphatase of Regenerating Liver-3(PRL-3) Inhibition by Small-molecular Inhibitors 被引量:2
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作者 SHEN Xing-gui SUN Li-wen +5 位作者 JIAO Ming LI Zhao-fa ZHAO Zhi-zhuang LI Qing-shan FU Xue-qi HUANG Zhong-xiu 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2006年第2期221-224,共4页
Phosphatase of Regenerating Liver-3 (PRL-3) is a newly identified colorectal cancer metastasis-related protein, which is a 22 kDa non-classical protein tyrosine phosphatase with a C-terminal prenylation motif. In th... Phosphatase of Regenerating Liver-3 (PRL-3) is a newly identified colorectal cancer metastasis-related protein, which is a 22 kDa non-classical protein tyrosine phosphatase with a C-terminal prenylation motif. In this study, the inhibition kinetics of protein tyrosine phosphatases(PTPs) by a fluorescent substrate, 6,8-difluoro-4-methylumbelliferyl phosphate(DiFMUP) was evaluated. PRL-3 exhibits classical Michaelis-Menten kinetics with a Vmax value of 11.3 μmol · L^-l · min^-1 Analysis of PRL-3 by a Michaelis-Menten plot and a double-reciprocal plot indicated that the inhibitor magnolol can cause Km to increase, but does not alter the Vmax value, which suggests the competitive inhibition of PRL-3. At the same time, it was found that DiFMUP is a more sensitive substrate for PRL-3 than para-nitrophenyl phosphate(pNPP) that is more frequently used at present. Furthermore, the method of screening for PTPs by the use of DiFMUP was developed, which studied the acceptance of DiFMUP by other PTPs. 展开更多
关键词 PRL-3 DiFMUP KINETICS INHIBITOR
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