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Expression, purification and biological effect of a novel single chain Fv antibody and protamine fusion protein for the targeted delivery of siRNAs to FGFR3 positive cancer cells
Zang, Chongsen; Liu, Zixuan; Yang, Kunmeng; Li, Rui; Wang, Xinxin; Zhang, Jizhou; Xiao, Yechen.
Affiliation
  • Zang, Chongsen; Jilin University. College of Basic Medical Science. Department of Biochemistry and Molecular Biology. Changchun. CN
  • Liu, Zixuan; Jilin University. College of Basic Medical Science. Department of Biochemistry and Molecular Biology. Changchun. CN
  • Yang, Kunmeng; High School Attached to Northeast Normal University. Changchun. CN
  • Li, Rui; Jilin University. School of Public Health. Department of Radiology. Changchun. CN
  • Wang, Xinxin; Jilin University. College of Basic Medical Science. Department of Biochemistry and Molecular Biology. Changchun. CN
  • Zhang, Jizhou; Jilin University. College of Basic Medical Science. Department of Biochemistry and Molecular Biology. Changchun. CN
  • Xiao, Yechen; Jilin University. College of Basic Medical Science. Department of Biochemistry and Molecular Biology. Changchun. CN
Electron. j. biotechnol ; Electron. j. biotechnol;28: 14-19, July. 2017. ilus, graf
Article in En | LILACS | ID: biblio-1015726
Responsible library: CL1.1
ABSTRACT

Background:

Gain-of-function of fibroblast growth factor receptor 3 (FGFR3) is involved in the pathogenesis of many tumors. More and more studies have focused on the potential usage of therapeutic single-chain Fv (ScFv) antibodies against FGFR3. RNA interference (RNAi) has been considered as a promising therapeutic method against cancer. A tool which can deliver small interference RNAs (siRNAs) into FGFR3 positive cancer cells is very promising for anti-tumor therapy.

Results:

In this study, a novel fusion protein R3P, which consists of FGFR3-ScFv and protamine, was generated in Escherichia coli by inclusion body expression strategy and Ni-NTA chromatography. Its yield reached 10 mg per liter of bacterial culture and its purity was shown to be higher than 95%. 1 µg of R3P could efficiently bind to about 2.5 pmol siRNAs and deliver siRNAs into FGFR3 positive RT112 and K562 cells. Annexin V staining results showed that R3P can deliver the amplified breast cancer 1 (AIB1) siRNAs to induce RT112 cell apoptosis.

Conclusion:

These results indicated that R3P was a promising carrier tool to deliver siRNAs into FGFR3 positive cancer cells and to exert anti-tumor effect.
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Full text: 1 Index: LILACS Main subject: Urinary Bladder Neoplasms / Recombinant Fusion Proteins / Single-Chain Antibodies Language: En Journal: Electron. j. biotechnol Journal subject: BIOTECNOLOGIA Year: 2017 Type: Article / Project document

Full text: 1 Index: LILACS Main subject: Urinary Bladder Neoplasms / Recombinant Fusion Proteins / Single-Chain Antibodies Language: En Journal: Electron. j. biotechnol Journal subject: BIOTECNOLOGIA Year: 2017 Type: Article / Project document