The enhanced effect of nuclear localization signal peptide during the ultrasound targeted microbubbles destruction mediated gene transfection

转染 核定位序列 分子生物学 NLS公司 琼脂糖凝胶电泳 微气泡 绿色荧光蛋白 荧光显微镜 流式细胞术 医学
作者
Sheng Cao,Qing Zhou,Jinling Chen,Yijia Wang,Nan Jiang,Qing Deng
出处
期刊:Chinese Journal of Ultrasonography [Chinese Medical Association]
卷期号:25 (3): 252-257
标识
DOI:10.3760/cma.j.issn.1004-4477.2016.03.018
摘要

Objective To investigate the transfection efficiency combining ultrasound targeted microbubbles destruction (UTMD) and nuclear localization signal (NLS) peptide for facilitating the plasmid of enhanced green fluorescent protein (pEGFP) into nucleus. Methods This study was divided into 3 groups, group A: UTMD+ pEGFP; group B: UTMD+ NLS+ pEGFP; group C: Lipo3000+ pEGFP. The NLS was labeled by FITC and pEGFP was marked by Cy3. The different mole ratio was adjusted between NLS and pEGFP for observing the best ratio of combination.The human umbilical vein endothelial cells (HUVEC) were transfected by the optimum ultrasonic irradiation parameters and the optimal NLS/pEGFP mole ratio. Six hours after transfection, the rate of Cy3 labeled pDNA into cells and nuclear were detected by flow cytometer and laser confocal microscope respectively. Forty-eight hours after transfection, the transfection efficiency was detected by flow cytometer; the survival rate of cells was measured by CCK8. RT-PCR and Western technology were used to detect the relative expression amount of mRNA and protein. The above indicators were compared among 3 groups, which were used to evaluate the enhanced effect of NLS in UTMD mediated gene transfection. Results ①Six hours after transfection, the NLS with green fluorescence and pEGFP with red fluorescence can show at the same site and signal intensity within the cell, that suggested a combination between them, agarose gel electrophoresis showed that the best molar ratio of NLS/pEGFP combining was 104∶1. ②Six hours after transfection, the rates of pEGFP into the cells were (63±12)%, (80±10)% and (92±8)%; the rates of pEGFP into the nucleus were (17±3)%, (50±12)% and (35±8)% in 3 groups respectively(P 80% in all groups; the transfection efficiency, relative quantity of mRNA and protein expression were increased gradually. There were significant differences among 3 groups(P<0.05). They were 1.6, 2.3 and 2.4 times in group B than those in group A, still lower than those in group C. Conclusions The UTMD combining NLS can promote the pEGFP into nucleus for improving the transfection efficiency. The NLS peptide can play an enhanced effect as a new strategy of UTMD. Key words: Sonication; Microbubbles; Transfection; Nuclear localization signal

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
桐桐应助小易采纳,获得10
刚刚
HThree完成签到 ,获得积分10
刚刚
刚刚
67完成签到,获得积分10
刚刚
杜欣然完成签到,获得积分10
1秒前
小羊完成签到 ,获得积分10
1秒前
沫沫发布了新的文献求助30
1秒前
2秒前
科研通AI6.4应助科研小白采纳,获得10
2秒前
车厘子完成签到 ,获得积分10
2秒前
cm357558984发布了新的文献求助10
2秒前
高高发布了新的文献求助10
3秒前
干净海亦发布了新的文献求助10
3秒前
3秒前
徐佳乐完成签到,获得积分10
3秒前
Sylus完成签到,获得积分20
3秒前
楠楠发布了新的文献求助10
3秒前
4秒前
4秒前
4秒前
左贵辉发布了新的文献求助10
5秒前
poppy发布了新的文献求助10
5秒前
5秒前
阿泓发布了新的文献求助10
5秒前
5秒前
凉皮DOG完成签到 ,获得积分20
5秒前
aajhajkahna应助goal采纳,获得10
5秒前
6秒前
Akim应助growl采纳,获得10
6秒前
aurora完成签到,获得积分10
6秒前
丰富时光完成签到,获得积分10
6秒前
6秒前
Sylus发布了新的文献求助10
7秒前
无私啤酒完成签到,获得积分10
7秒前
从嘉完成签到,获得积分10
7秒前
HUQ发布了新的文献求助10
7秒前
7秒前
乐乐应助yangts2021采纳,获得10
9秒前
zzzzzz发布了新的文献求助10
9秒前
高分求助中
Markov Chain Monte Carlo 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Common Foundations of American and East Asian Modernisation: From Alexander Hamilton to Junichero Koizumi 5000
Pediatric Dermoscopy Trichoscopy & Onychoscopy 2030
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
Handbuch Trainingswissenschaft – Trainingslehre 500
Additive Manufacturing Design and Applications (ASM Handbook, Volume 24A) 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7575233
求助须知:如何正确求助?哪些是违规求助? 9154670
关于积分的说明 19583580
捐赠科研通 7159380
什么是DOI,文献DOI怎么找? 3264673
关于科研通互助平台的介绍 2429991
邀请新用户注册赠送积分活动 2255071