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
lizishu应助优零采纳,获得10
刚刚
量子星尘发布了新的文献求助10
1秒前
酷波er应助哇哈哈哈哈哈采纳,获得10
2秒前
2秒前
口口完成签到,获得积分10
2秒前
jsl完成签到,获得积分10
2秒前
2秒前
lijiaqi发布了新的文献求助10
2秒前
2秒前
核桃发布了新的文献求助10
2秒前
Avatar完成签到,获得积分10
3秒前
石龙子完成签到,获得积分10
3秒前
3秒前
shuaiyuancheng完成签到,获得积分20
3秒前
3秒前
ding应助ymq156采纳,获得30
4秒前
liangyong发布了新的文献求助10
4秒前
我要吃羊肉粉完成签到,获得积分20
5秒前
5秒前
研友_ZeoKYL应助RS6采纳,获得10
5秒前
5秒前
健忘的妙松完成签到,获得积分10
5秒前
5秒前
xumou完成签到 ,获得积分10
6秒前
6秒前
隐形曼青应助Cassity采纳,获得30
6秒前
今后应助peterhent采纳,获得10
8秒前
halsuen完成签到,获得积分10
8秒前
anti1988完成签到,获得积分10
8秒前
8秒前
sky011221完成签到,获得积分10
9秒前
活力安南发布了新的文献求助10
9秒前
9秒前
balabala完成签到,获得积分10
9秒前
嘿嘿完成签到 ,获得积分10
10秒前
10秒前
今后应助maodoudou采纳,获得10
10秒前
james发布了新的文献求助30
10秒前
斯文败类应助佟碧玉采纳,获得10
10秒前
林霖完成签到 ,获得积分10
10秒前
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
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Contemporary Debates in Epistemology (3rd Edition) 1000
International Arbitration Law and Practice 1000
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6160270
求助须知:如何正确求助?哪些是违规求助? 7988515
关于积分的说明 16604990
捐赠科研通 5268587
什么是DOI,文献DOI怎么找? 2811111
邀请新用户注册赠送积分活动 1791266
关于科研通互助平台的介绍 1658124