Background-Free Imaging of a Viral Capsid Proteins Coated Anisotropic Nanoparticle on a Living Cell Membrane with Dark-Field Optical Microscopy

• Published in: Analytical chemistry (Washington) 2018-01, Vol.90 (2), p.1177-1185
• Main Authors: Ye, Zhongju, Wei, Lin, Zeng, Xuyao, Weng, Rui, Shi, Xingbo, Wang, Naidong, Chen, Langxing, Xiao, Lehui
• Format: Article
• Language: English
• Subjects: Anchoring; Anisotropy; Biocompatibility; Capsid Proteins - analysis; Cells; Cells (biology); Chemistry; Circoviridae Infections - pathology; Circoviridae Infections - virology; Circovirus - chemistry; Diffusion; Digital imaging; Equipment Design; Gaussian process; Gold; Gold - chemistry; Hep G2 Cells; Hepatocytes - pathology; Hepatocytes - virology; Humans; Image analysis; Image contrast; Image processing; Inspection; Metal Nanoparticles - chemistry; Microscopy; Microscopy - instrumentation; Microscopy - methods; Nanoparticles; Nanorods; Normal distribution; Optical Imaging - instrumentation; Optical Imaging - methods; Optical microscopy; Organelles; Polarization; Proteins; Scattering; Surface chemistry
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.7b03762

Exploring the diffusion dynamics of a viral capsid proteins (VCP)-functionalized nanocarrier on a living cell membrane could provide much kinetic information for the better understanding of their biological functionality. Gold nanoparticles are an excellent core material of nanocarriers because of the good biocompatibility as well as versatile surface chemistry. However, due to the strong scattering background from subcellular organelles, it is a grand challenge to selectively image an individual nanocarrier on a living cell membrane. In this work, we demonstrated a convenient strategy to effectively screen the scattering background from living cells for single-particle imaging with a polarization-resolved dual-channel imaging module. By taking advantage of the polarization of anisotropic gold nanoparticles (gold nanorods, GNRs), the signals from cell components could be counteracted after subtracting the sequential images one by one, while those transiently rotating GNRs on the cell membrane still exist in the processed image. In contrast to the previously reported methods, this method does not require a complicated optical setup alignment and sophisticated digital image analysis process. According to the single-particle imaging results, the majority of VCP–GNRs were anchoring on the cell membrane with confined diffusion. Interestingly, on further inspection of the diffusion trajectories, the particles displayed anomalous confined diffusion with randomly distributed large walking steps during the whole track. Non-Gaussian step distribution was noted, indicating heterogeneous binding and desorption processes on the cell membrane. As a consequence of the robust background screening capability, this approach would find broad applications for single-particle imaging under a noisy environment, e.g., living cells.