4.6 Article

Label-Free Imaging of Nanoscale Displacements and Free-Energy Profiles of Focal Adhesions with Plasmonic Scattering Microscopy

Journal

ACS SENSORS
Volume 6, Issue 11, Pages 4244-4254

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c01938

Keywords

surface plasmon resonance; plasmonic scattering microscopy; cell physiology; surface interactions; plasma membrane

Funding

  1. National Institutes of Health [R01GM107165]
  2. NSF program [NNCI-ECCS-1542160]

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Cell adhesion is crucial for cell functions, and plasmonic scattering microscopy (PSM) can directly image single focal adhesions with sub-micrometer spatial resolution. PSM offers high signal-to-noise ratio and enables super-resolution lateral localization and precise tracking of vertical distances for analyzing free-energy profiles. PSM provides insights into focal adhesion activities and serves as a promising tool for investigating cell/surface interactions and tissue adhesive materials screening.
Cell adhesion plays a critical role in cell communication, cell migration, cell proliferation, and integration of medical implants with tissues. Focal adhesions physically link the cell cytoskeleton to the extracellular matrix, but it remains challenging to image single focal adhesions directly. Here, we show that plasmonic scattering microscopy (PSM) can directly image the single focal adhesions in a label-free, real-time, and non-invasive manner with sub-micrometer spatial resolution. PSM is developed based on surface plasmon resonance (SPR) microscopy, and the evanescent illumination makes it immune to the interference of intracellular structures. Unlike the conventional SPR microscopy, PSM can provide a high signal-tonoise ratio and sub-micrometer spatial resolution for imaging the analytes with size down to a single-molecule level, thus allowing both the super-resolution lateral localization for measuring the nanoscale displacement and precise tracking of vertical distances between the analyte centroid and the sensor surface for analysis of free-energy profiles. PSM imaging of the RBL-2H3 cell with temporal resolution down to microseconds shows that the focal adhesions have random diffusion behaviors in addition to their directional movements during the antibody-mediated activation process. The freeenergy mapping also shows a similar movement tendency, indicating that the cell may change its morphology upon varying the binding conditions of adhesive structures. PSM provides insights into the individual focal adhesion activities and can also serve as a promising tool for investigating the cell/surface interactions, such as cell capture and detection and tissue adhesive materials screening.

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