探討抗菌胜肽攜帶干擾核糖核酸於細胞抑制基因效率; Delivery of short interfering RNA using antimicrobial peptides

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Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/61420

Title:	探討抗菌胜肽攜帶干擾核糖核酸於細胞抑制基因效率;Delivery of short interfering RNA using antimicrobial peptides
Authors:	蔡勝凱;Tsai,Sheng-Kai
Contributors:	化學工程與材料工程學系
Keywords:	干擾核糖核酸;抗菌胜肽;siRNA;antimicrobial peptide
Date:	2013-08-29
Issue Date:	2013-10-08 15:08:05 (UTC+8)
Publisher:	國立中央大學
Abstract:	Small interfering RNA (siRNA)具有專一性有效抑制特定基因表現的功能，然而它本身帶負電的緣故，無法有效接近帶負電的細胞膜、進去細胞質發揮正常功能。所以需要一個合適的載體把siRNA包覆，防止siRNA被降解和進入細胞。本研究利用Indolicidin(IL)以及其衍生物ILF89、PEI(M.W=25k da)-ILC、PEI(M.W=25k da)-CIL、PEI(M.W=750k da)-ILC以及PEI(M.W=750k da)-CIL作為基因載體。檢測出IL-siRNA和ILF89-siRNA粒徑大小分別為大約800-1000nm和300-600nm而在表面電位的部分IL-siRNA complex在小於N/P=20是呈現中性和負電，大於N/P=30以上則是18mV以上 ILF89其表面電位都呈現負電。以相同的配製方法對HEK293T這株細胞的基因-GAPDH(每個動物細胞都含有此基因)去做抑制實驗，IL、ILF89利用QPCR分析出來的實驗結果大約是30-40％和幾乎0％的mRNA抑制效果比預期的來的低。針對另一株細胞HT1080的基因-EGFP，以Flow cytometry分析螢光螢光蛋白質的表現，IL、ILF89當成載體攜帶siRNA其螢光幾乎沒有下降。原因是EGFP的半生期過長，長達26小時，蛋白質很穩定以致於抑制效果非常的不明顯。以PEI(M.W=25k da)-ILC、PEI(M.W=25k da)-CIL、PEI(M.W=750k da)-ILC以及PEI(M.W=750k da)-CIL作為基因載體，分析的結果PEI接上IL的抑制效果都比PEI好 PEI(M.W=25k da)-IL的抑制效果則是比PEI(M.W=750 da)好。 IL、ILF89作為基因載體抑制效果沒有預期的高，然而PEI以共價鍵和IL相接，效果比PEI好，所以IL有發揮提高轉染的效果。 Small interfering RNA (siRNA) can specifically inhibit certain gene expression, but siRNA cannot approach to negatively-charged cell membrane and not even be functionalized into cytoplasm. To overcome the above problems, a suitable carrier to cover siRNA from degradation and to deliver it into cell is required. In this study, we selected Indolicidin(IL), its derivative ILF89, PEI(M.W=25k da)-ILC、PEI(M.W=25k da)-CIL、PEI(M.W=750k da)-ILC以及PEI(M.W=750k da)-CIL as the gene carriers. Indolicidin may assemble into a complex with siRNA by electrostatic interaction at different amine over phosphate molar ratio (N/P ratio). First, we covered siRNA with IL and ILF89, and found that the sizes of siRNA-peptide complex are 800nm to 1000nm and 300nm to 600nm, respectively. On the other hand, the zeta potential of siRNA-IL complex at N/P ratio less than 20 is neutral and negatively charged while that of N/P ratio higher than 30 is above 18mV. In contrast to siRNA-IL complex, zeta potential of siRNA-ILF89 complex is completely negatively charged. We applied the above method to the inhibitory examination on glyceraldehyde 3-phosphate dehydrogenase (GAPDH) gene of HEK293T cell line. From the real-time polymerase chain reaction (QPCR) analysis, we found that the inhibitory efficiencies of siRNA-IL and siRNA-ILF89 complex are 30% to 40% of mRNA and 0％ of mRNA, respectively, which is relatively lower than the expected result. To another gene, enhanced green fluorescent protein (EGFP), expressed from HT1080 cell line, there is little decrease in the fluorescence intensity from the green fluorescent protein expression of both siRNA-IL and siRNA-ILF89 complex, which was analyzed by QPCR. We attributed the above results to the long half-life of EGFP (26 hour) that makes the protein stable resulting in low inhibitory efficiency. From results of PEI-IL, we found that the inhibitory efficiencies of PEI-IL are higher than PEI and the inhibitory efficiencies of PEI(M.W=25kda)-IL are higher than PEI(M.W=750kda)-IL. Thus, IL shows enhanced transfection ability.
Appears in Collections:	[National Central University Department of Chemical & Materials Engineering] Electronic Thesis & Dissertation

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