کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9774627 | 1509090 | 2005 | 13 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Evaluation of cell penetrating peptides fused to elastin-like polypeptide for drug delivery
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کلمات کلیدی
PBSRFUPenetratinMβCDMTSELPPNACPPPeptide nucleic acid - اسید نوکلئیک پپتیدTAT - تاتDrug delivery - تحویل(رهایش) داروPhosphate buffered saline - فسفات بافر شورmethyl-β-cyclodextrin - متیل-β-سیکلوکودکسترینAntp - مزهRelative Fluorescence Units - واحد فلورسانس نسبیElastin-like polypeptide - پلی پپتید مانند پلی استرcell penetrating peptide - پپتید نفوذ سلولی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
بیومتریال
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Evaluation of cell penetrating peptides fused to elastin-like polypeptide for drug delivery Evaluation of cell penetrating peptides fused to elastin-like polypeptide for drug delivery](/preview/png/9774627.png)
چکیده انگلیسی
Translocation through the plasma membrane is a major limiting step for the cellular delivery of macromolecules. Several cell penetrating peptides (CPP) have been demonstrated to efficiently internalize various molecular cargo to targets inside eukaryotic cells. In this study, the efficiency and mechanism of cellular uptake of the CPPs penetratin, Tat, and MTS fused to elastin-like polypeptides (CPP-ELP) were evaluated. Elastin-like polypeptides are biopolymers with features that make them useful as polymeric carriers for the delivery of therapeutics. Therefore, improving efficiency of cellular uptake by fusing ELPs to CPPs and understanding the mechanism of their cellular internalization could contribute to development of new therapeutic approaches. Flow cytometry and confocal fluorescence microscopy were used to elucidate the mechanism of CPP-ELP uptake. The internalization of all CPP-ELPs was impaired dramatically at 4 °C, under ATP depletion conditions, and with hyperosmolar sucrose, implicating involvement of an endocytic pathway for CPP-ELP internalization. Penetratin was identified as the most effective CPP for delivering ELP. Finally, in order to demonstrate the potential of CPP-ELP for drug delivery, a fusion polypeptide was made containing penetratin, ELP, and a peptide derived from the cyclin-dependent kinase inhibitor p21. This polypeptide was shown to inhibit proliferation of SKOV-3 and HeLa cells by slowing their growth rate.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Controlled Release - Volume 108, Issues 2â3, 28 November 2005, Pages 396-408
Journal: Journal of Controlled Release - Volume 108, Issues 2â3, 28 November 2005, Pages 396-408
نویسندگان
Iqbal Massodi, Gene L. III, Drazen Raucher,