4.8 Article

Measurement of Protein-Protein Interaction Dynamics Using Microfluidics and Particle Diffusometry

期刊

ANALYTICAL CHEMISTRY
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c02570

关键词

-

资金

  1. National Institutes of Health (NIH) National Institute of Allergy and Infectious Diseases (NIAID) [R61AI140474]
  2. National Cancer Institute (NCI) [R01CA246315]
  3. National Science Foundation (NSF) CAREER award [1752366]
  4. Div Of Chem, Bioeng, Env, & Transp Sys
  5. Directorate For Engineering [1752366] Funding Source: National Science Foundation

向作者/读者索取更多资源

Measuring and optimizing protein-protein interactions are crucial in biomolecular sciences and engineering. We developed a new method based on microfluidics and particle diffusometry that is simple to operate and as accurate as the current gold standard.
The measurement and optimization of protein-protein interactions are critical in the design of biotherapeutics, biomolecular sensing elements, and functional protein-based biomaterials among other biomolecular sciences and engineering. Current gold standard assays require specifically designed core facilities, equipment, and expertise to implement the measurement, making it inconvenient for most labs unless implemented routinely. We developed a new method aiming at measuring protein binding kinetics based on microfluidics and particle diffusometry (PD), which only needs very general lab equipment, including a fluorescence microscope, a syringe pump, and a simple microchannel fabricated on a glass slide. Protein binding pairs are immobilized on two kinds of nanoparticles with different diameters using widely available conjugation chemistries. The two diluted particle suspensions are injected using a syringe pump into a Y-junction microchannel, where they bind and form particle complexes with increasing size, thereby decreasing particles' Brownian motion amplitude and diffusivity, which can be detected by PD. By taking images at a series of specific points along the microchannel, the particle diffusivity is measured at different time points after the introduction of protein-protein binding. These data are then used to quantify the protein binding kinetic constant. This label-free particle-based method is simple to operate and as accurate as the current gold standard. We demonstrate the feasibility of this accessible method by quantifying the streptavidin-biotin association constant (1.74 +/- 0.51 x 107 M-1 s-1), which compares well with previously published results.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据