Detecting Individual Proteins and Their Surface Charge Variations in Solution by the Potentiometric Nanoimpact Method

التفاصيل البيبلوغرافية
العنوان: Detecting Individual Proteins and Their Surface Charge Variations in Solution by the Potentiometric Nanoimpact Method
المؤلفون: Popular Pandey, Nisha Bhattarai, Linjia Su, Xuewen Wang, Fenfei Leng, Bernard Gerstman, Prem P. Chapagain, Jin He
المصدر: ACS Sensors. 7:555-563
بيانات النشر: American Chemical Society (ACS), 2022.
سنة النشر: 2022
مصطلحات موضوعية: Fluid Flow and Transfer Processes, Process Chemistry and Technology, Static Electricity, Electrochemistry, Nanoparticles, Nanotechnology, Proteins, Bioengineering, Instrumentation
الوصف: Label-free detection and analysis of proteins in their natural form and their dynamic interactions with substrates at the single-molecule level are important for both fundamental studies and various applications. Herein, we demonstrate a simple potentiometric method to achieve this goal by detecting the native charge of protein in solution by utilizing the principle of single-entity electrochemistry techniques. When a charged protein moves near the vicinity of a floating carbon nanoelectrode connected to a high-impedance voltage meter, the distinct local electrostatic potential changes induced by the transient collision event of protein, also called the "nanoimpact" event, can be captured by the nanoelectrode as a potential probe. This potentiometric method is highly sensitive for charged proteins, and low-molecular-weight proteins less than 10 kDa can be detected in low-salt-concentration electrolytes. By analyzing the shape and magnitude of the recorded time-resolved potential change and its time derivative, we can reveal the charge and motion of the protein in the nonspecific protein-surface interaction event. The charge polarity variations of the proteins at different pH values were also successfully probed. Compared with synthetic spherical nanoparticles, the statistical analysis of many single-molecule nanoimpact events revealed a large variation in the recorded transient potential signals, which may be attributed to the intrinsic protein dynamics and surface charge heterogeneity, as suggested by the finite element method and molecular dynamic simulations.
تدمد: 2379-3694
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b625c7de10613b60e09b1d0464d49a4d
https://doi.org/10.1021/acssensors.1c02385
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....b625c7de10613b60e09b1d0464d49a4d
قاعدة البيانات: OpenAIRE