基本信息
浏览量:52
职业迁徙
个人简介
Research Interests
Optical Semi-noninvasive Glucose Sensor
Schematics illustrating the principles of the fluorescence affinity hollow fiber sensor. In the absence of glucose, fluorochromelabeled Concanavalin A is bound to fixed glucose residues inside porous beads (left hand). The beads are colored with dyes that prevent the excitation light from penetrating into them and inducing Con A to fluoresce, thus keeping the fluorescence emission at 520 nm. After diffusion of glucose through the hollow fiber membrane (molecular weight cutoff, 10 kDa), Con A is displaced from the beads and diffuses out of them, and hereby fluorochrome-labeled Con A becomes exposed to excitation light resulting in a strong increase in fluorescence (right hand).
Design of a GIP (glucose indicator protein) for sensing glucose based on FRET. (a) Diagram of the GIP structure showing how FRET between two GFPs can measure glucose concentration. The GBP adopts an “open” form in the presence of the glucose, which triggers a conformation change, causing two GFPs apart from the center of GBP leading to the change in FRET. The (b) represents one molecule of the glucose bound onto the binding cleft of the GBP.
Optical Semi-noninvasive Glucose Sensor
Schematics illustrating the principles of the fluorescence affinity hollow fiber sensor. In the absence of glucose, fluorochromelabeled Concanavalin A is bound to fixed glucose residues inside porous beads (left hand). The beads are colored with dyes that prevent the excitation light from penetrating into them and inducing Con A to fluoresce, thus keeping the fluorescence emission at 520 nm. After diffusion of glucose through the hollow fiber membrane (molecular weight cutoff, 10 kDa), Con A is displaced from the beads and diffuses out of them, and hereby fluorochrome-labeled Con A becomes exposed to excitation light resulting in a strong increase in fluorescence (right hand).
Design of a GIP (glucose indicator protein) for sensing glucose based on FRET. (a) Diagram of the GIP structure showing how FRET between two GFPs can measure glucose concentration. The GBP adopts an “open” form in the presence of the glucose, which triggers a conformation change, causing two GFPs apart from the center of GBP leading to the change in FRET. The (b) represents one molecule of the glucose bound onto the binding cleft of the GBP.
研究兴趣
论文共 193 篇作者统计合作学者相似作者
按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
Yadin David,Jerome Schultz
Global Clinical Engineering Journalno. 1 (2020): 33-43
Journal of Diabetes Science and Technologyno. 1 (2015): 153-155
A. D. Pant,K. Nagamine, I. Shiraki,E. Torikai,K. Shimomura,F. L. Pratt,H. Ariga, K. Ishida,J. S. Schultz
13TH INTERNATIONAL CONFERENCE ON MUON SPIN ROTATION, RELAXATION AND RESONANCE (2014)
加载更多
作者统计
#Papers: 192
#Citation: 7071
H-Index: 41
G-Index: 81
Sociability: 6
Diversity: 0
Activity: 0
合作学者
合作机构
D-Core
- 合作者
- 学生
- 导师
数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn