Plasmonic scattering imaging of single proteins and binding kinetics

• Published in: Nature methods Vol. 17; no. 10; pp. 1010 - 1017
• Main Authors: Zhang, Pengfei, Ma, Guangzhong, Dong, Wei, Wan, Zijian, Wang, Shaopeng, Tao, Nongjian
• Format: Journal Article
• Language: English
• Published: New York Nature Publishing Group US 01-10-2020; Nature Publishing Group
• Subjects: 631/1647/2196; 631/1647/245/2226; 631/57/2265; Antibodies; Binding; Bioinformatics; Biological Microscopy; Biological Techniques; Biomedical and Life Sciences; Biomedical Engineering/Biotechnology; Gold; Heterogeneity; Humans; Imaging; Immunoglobulin A - chemistry; Immunoglobulin A - metabolism; Immunoglobulin M - chemistry; Immunoglobulin M - metabolism; Kinetics; Life Sciences; Measuring instruments; Plasmonics; Protein Binding; Protein Interaction Mapping - methods; Proteins; Proteins - chemistry; Proteins - metabolism; Proteomics; Resonance scattering; Single Molecule Imaging; Surface Plasmon Resonance
• ISSN: 1548-7091; 1548-7105
• DOI: 10.1038/s41592-020-0947-0

Measuring the binding kinetics of single proteins represents one of the most important and challenging tasks in protein analysis. Here we show that this is possible using a surface plasmon resonance (SPR) scattering technique. SPR is a popular label-free detection technology because of its extraordinary sensitivity, but it has never been used for imaging single proteins. We overcome this limitation by imaging scattering of surface plasmonic waves by proteins. This allows us to image single proteins, measure their sizes and identify them based on their specific binding to antibodies. We further show that it is possible to quantify protein binding kinetics by counting the binding of individual molecules, providing a digital method to measure binding kinetics and analyze heterogeneity of protein behavior. We anticipate that this imaging method will become an important tool for single protein analysis, especially for low volume samples, such as single cells.
Plasmonic scattering microscopy (PSM) enables the imaging of single proteins on SPR instruments. The method enables measurement of protein size and binding kinetics and is fully compatible with simultaneous traditional SPR measurements.