Protein adsorption by nanomechanical mass spectrometry: Beyond the real-time molecular weighting

被引:4
|
作者
Stachiv, Ivo [1 ]
Kuo, Chih-Yun [2 ,3 ,4 ]
Li, Wei [1 ]
机构
[1] Czech Acad Sci, Inst Phys, Dept Funct Mat, Prague, Czech Republic
[2] Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic
[3] Charles Univ Prague, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic
[4] Charles Univ Prague, Gen Univ Hosp Prague, Prague, Czech Republic
关键词
protein adsorption; molecule mechanical properties; molecular weight; protein detection; mass spectrometry; mass sensing; RESONATORS; NANOPARTICLES; FREQUENCY;
D O I
10.3389/fmolb.2022.1058441
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During past decades, enormous progress in understanding the mechanisms of the intermolecular interactions between the protein and surface at the single-molecule level has been achieved. These advances could only be possible by the ongoing development of highly sophisticated experimental methods such as atomic force microscopy, optical microscopy, surface plasmon resonance, ellipsometry, quartz crystal microbalance, conventional mass spectrometry, and, more recently, the nanomechanical systems. Here, we highlight the main findings of recent studies on the label-free single-molecule (protein) detection by nanomechanical systems including those focusing on the protein adsorption on various substrate surfaces. Since the nanomechanical techniques are capable of detecting and manipulating proteins even at the single-molecule level, therefore, they are expected to open a new way of studying the dynamics of protein functions. It is noteworthy that, in contrast to other experimental methods, where only given protein properties like molecular weight or protein stiffness can be determined, the nanomechanical systems enable a real-time measurement of the multiple protein properties (e.g., mass, stiffness, and/or generated surface stress), making them suitable for the study of protein adsorption mechanisms. Moreover, we also discuss the possible future trends in label-free detection and analysis of dynamics of protein complexes with these nanomechanical systems.
引用
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页数:8
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