Abstract |
To enhance the penetration of P53 into tumor cells by fusion it with the cell penetrating peptide 9R. The fusion gene of 9R-p53 was cloned into the expression vector. The fusion protein, CPPs-P53, was expressed and purified. We detected the rate of cell growth inhibition and apoptosis by MTT and Annexin-V-FITC/PI double stained method respectively for measuring its effect on tumor cells. CPPs-P53 and P53 were successfully expressed and purified, the purity of both proteins reached up to 90%. MTT assay showed that the cell growth inhibition by CPPs-P53 was more efficient than P53, and the rate of cell growth inhibition is dose-dependent. The apoptosis experiment showed that P53 could induce apoptosis of tumor cells. Compared with the P53, CPPs-P53 had a more significant effect in inducing cell apoptosis (**P < 0.01). The CPPs-P53 shows more significant effects than P53 in inhibiting cell growth and inducing apoptosis on tumor cells.
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Authors | Yuan Liu, Rui Chen, Nan Zhang, Xianlong Ye, Yin Bai, Yuquan Wei, Guiping Ren, Deshan Li |
Journal | Sheng wu gong cheng xue bao = Chinese journal of biotechnology
(Sheng Wu Gong Cheng Xue Bao)
Vol. 29
Issue 7
Pg. 955-64
(Jul 2013)
ISSN: 1000-3061 [Print] China |
PMID | 24195362
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cell-Penetrating Peptides
- Tumor Suppressor Protein p53
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Topics |
- Apoptosis
- Cell Line, Tumor
- Cell-Penetrating Peptides
(pharmacology)
- Humans
- Tumor Suppressor Protein p53
(pharmacology)
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