Glucose oxidase-like activity of cerium oxide nanoparticles: use for personal glucose meter-based label-free target DNA detection

葡萄糖计 葡萄糖氧化酶 放大器 葡萄糖酸 化学 大肠杆菌 组合化学 聚合酶链反应 DNA 生物化学 生物物理学 生物传感器 糖尿病 基因 生物 内分泌学
作者
Hyo Yong Kim,Ki Soo Park,Hyun Gyu Park
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:10 (10): 4507-4514 被引量:38
标识
DOI:10.7150/thno.41484
摘要

Recently, personal glucose meter (PGM) has been utilized for the detection of non-glucose targets for point-of-care (POC) testing.Aimed at this goal, we herein developed a new PGM-based label-free read-out method for polymerase chain reaction (PCR) based on our novel finding that cerium oxide nanoparticles (CeO2 NPs) exhibit glucose oxidase-like activity comparable to the natural glucose oxidase enzyme.Methods: In principle, DNA amplicons produced by PCR in the presence of target DNA electrostatically bind to CeO2 NPs, leading to their aggregation and reducing the efficiency for CeO2 NP-catalyzed glucose oxidation reaction.Thus, glucose is hardly oxidized to gluconic acid, resulting in the maintenance of initial high glucose level.On the contrary, in the absence of target DNA or presence of non-target DNA, DNA amplicons are not produced and glucose is effectively oxidized by the glucose oxidase-like activity of CeO2 NPs, leading to the significant reduction of glucose level.Finally, the resulting glucose level is simply measured by using PGM.Results: With this strategy, DNA amplicons were quantitatively examined within 5 min, realizing ultrafast analysis of PCR results without any cumbersome and labor-intensive procedures.In addition, the target genomic DNA derived from Escherichia coli (E.coli) was sensitively determined down to 10 copies with high selectivity.Conclusion: Importantly, the use of PGM as a detection component enables its direct application in POC settings.Based on the meritorious features of PGM such as rapidity, simplicity, and cost-effectiveness, we expect that the devised system could serve as a core platform for the on-site read-out of PCR amplification.
最长约 10秒,即可获得该文献文件

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
Orange应助guangshuang采纳,获得10
刚刚
NIDADI完成签到,获得积分20
刚刚
kk0612完成签到,获得积分20
1秒前
1秒前
Summer发布了新的文献求助10
2秒前
无花果应助墨秘一采纳,获得10
3秒前
3秒前
跳跃奇迹完成签到,获得积分10
3秒前
kk0612发布了新的文献求助10
3秒前
3秒前
舒服的安想完成签到,获得积分10
4秒前
zzc完成签到,获得积分10
4秒前
5秒前
隐形曼青应助troyqiujing采纳,获得10
5秒前
6秒前
6秒前
领导范儿应助戈多采纳,获得10
7秒前
NIDADI发布了新的文献求助10
7秒前
正月初九完成签到,获得积分10
7秒前
跳跃奇迹发布了新的文献求助10
7秒前
钇铯完成签到,获得积分10
7秒前
喵了个咪完成签到 ,获得积分10
8秒前
田様应助HY采纳,获得10
8秒前
情怀应助忐忑的石头采纳,获得10
10秒前
蒋若风发布了新的文献求助10
10秒前
酷波er应助Binggo采纳,获得10
10秒前
乐乐应助清秀的迎彤采纳,获得10
10秒前
wwx发布了新的文献求助10
10秒前
11秒前
离明完成签到,获得积分20
11秒前
dfg完成签到,获得积分10
12秒前
丘比特应助夜信采纳,获得10
12秒前
大模型应助Jay采纳,获得10
12秒前
小王同学发布了新的文献求助10
12秒前
12秒前
ding应助牧歌采纳,获得10
13秒前
lkjh发布了新的文献求助10
13秒前
忧伤的听白完成签到,获得积分20
13秒前
13秒前
aaa发布了新的文献求助10
13秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2500
Continuum thermodynamics and material modelling 2000
Healthcare Finance: Modern Financial Analysis for Accelerating Biomedical Innovation 2000
Applications of Emerging Nanomaterials and Nanotechnology 1111
Les Mantodea de Guyane Insecta, Polyneoptera 1000
지식생태학: 생태학, 죽은 지식을 깨우다 700
Neuromuscular and Electrodiagnostic Medicine Board Review 700
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 纳米技术 内科学 物理 化学工程 计算机科学 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 电极
热门帖子
关注 科研通微信公众号,转发送积分 3468882
求助须知:如何正确求助?哪些是违规求助? 3061910
关于积分的说明 9077482
捐赠科研通 2752380
什么是DOI,文献DOI怎么找? 1510402
科研通“疑难数据库(出版商)”最低求助积分说明 697789
邀请新用户注册赠送积分活动 697759