Construction of expressing vectors including Mda-7 gene beside the RGD sequences for better tumor targeting
سال انتشار: 1392
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 734
فایل این مقاله در 10 صفحه با فرمت PDF قابل دریافت می باشد
- صدور گواهی نمایه سازی
- من نویسنده این مقاله هستم
استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
NBCI08_0568
تاریخ نمایه سازی: 29 شهریور 1394
چکیده مقاله:
Background and objective: Up to now, many researches has performed to improve the anti-tumoral effect of mda-7 protein. The purpose of our research is to adjoin anti-tumoral effect of mda-7 and RGD peptide targeting to improve apoptosis induction in tumor site especially liver related onesMaterials and methods: Mda-7 gene with two different RGD sequencees amplified by PCR and then cloned into TA – cloning system. Colonies including these genes selected with Blue – White Screening, colony PCR and sequencing respectively. After that the genes digested and sub - cloned into expression vector following confirmation by colony PCR and sequencing. In addition, these construct transfected into 293 and Huh-7 cells for further expression assay. Protein expression then evaluated by RT-PCR and IF ( Immunofluorescence Assay ).Results and conclusion: Three different Mda-7 with RGD terminal peptide, were cloned correctly into expression vector and its expression evaluated with IF, RT-PCR, which was suitable. It was shown that these proteins were expressed and secreted into culture media and the rate of expression is considerable in 293 and Huh-7 cells. Theoretically RGD tagged Mda-7 would be able to induce apoptosis more strongly than the standard one therefore these new constructs has the potential forfuture researches.
کلیدواژه ها:
نویسندگان
Seyed Younes Hosseini
Gastroenterohepatology Research Center (GEHRC) , shiraz University Of Medical Sciences .
Mahboobeh Khodadad
Gastroenterohepatology Research Center (GEHRC) , shiraz University Of Medical Sciences .Department Of Microbiology , Islamic Azad University , Jahrom Branch
Samaneh Bina
Institute of Biochemistry and Biophysics (IBB) , University Of Tehran .
Shahin Ahmadian
Institute of Biochemistry and Biophysics (IBB) , University Of Tehran .
مراجع و منابع این مقاله:
لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :