亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

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
DPH完成签到 ,获得积分10
1秒前
程浩发布了新的文献求助10
6秒前
Lyf完成签到 ,获得积分10
14秒前
Thanks完成签到 ,获得积分10
24秒前
27秒前
cloudyrose发布了新的文献求助10
32秒前
lysenko完成签到 ,获得积分10
47秒前
50秒前
54秒前
小马甲应助科研通管家采纳,获得30
54秒前
54秒前
李健应助科研通管家采纳,获得10
54秒前
SUnnnnn发布了新的文献求助10
57秒前
棉茶完成签到,获得积分10
1分钟前
张昭蓉完成签到,获得积分10
1分钟前
任性的白玉完成签到 ,获得积分10
1分钟前
可爱的函函应助SUnnnnn采纳,获得10
1分钟前
cloudyrose完成签到,获得积分10
1分钟前
1分钟前
Gheros完成签到,获得积分20
1分钟前
zqq完成签到,获得积分0
1分钟前
Gheros发布了新的文献求助10
1分钟前
今后应助anyway采纳,获得10
1分钟前
1分钟前
烟花应助xiaoxinbaba采纳,获得10
1分钟前
青柠完成签到 ,获得积分10
1分钟前
niuniuniu发布了新的文献求助60
1分钟前
852应助Gheros采纳,获得10
2分钟前
三点前我必睡完成签到 ,获得积分10
2分钟前
zsmj23完成签到 ,获得积分0
2分钟前
光亮静槐完成签到 ,获得积分10
2分钟前
2分钟前
xzy发布了新的文献求助10
2分钟前
思源应助xzy采纳,获得10
2分钟前
NexusExplorer应助NICOO采纳,获得10
2分钟前
3分钟前
3分钟前
含蓄绿竹发布了新的文献求助10
3分钟前
跳跃绿竹发布了新的文献求助10
3分钟前
高分求助中
(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
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
卤化钙钛矿人工突触的研究 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 610
2026 Hospital Accreditation Standards 500
脑电大模型与情感脑机接口研究--郑伟龙 400
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6268810
求助须知:如何正确求助?哪些是违规求助? 8090255
关于积分的说明 16910879
捐赠科研通 5338593
什么是DOI,文献DOI怎么找? 2840895
邀请新用户注册赠送积分活动 1818247
关于科研通互助平台的介绍 1671526