Immersion Mirau interferometry for label-free live cell imaging in an epi-illumination geometry

Oleksandra V Lyulko1, Gerhard Randers-Pehrson1, David J Brenner1

  • 1Center for Radiological Research, Columbia University, New York, NY 10533.

Insights

Immersion Mirau Interferometry (IMI) offers label-free imaging for living cells, avoiding UV-light damage. Simultaneous Immersion Mirau Interferometry (SIMI) overcomes vibration sensitivity, enabling high-quality cell imaging for experiments.

Area of Science:

  • Cell biology
  • Optical microscopy
  • Biophysics

Background:

  • Fluorescent stains and UV-light can damage cells during imaging.
  • Label-free imaging techniques are crucial for studying live cells.
  • Phase-shifting interferometry (PSI) is sensitive to environmental vibrations.

Purpose of the Study:

  • To develop and validate Immersion Mirau Interferometry (IMI) for label-free imaging of living cells in medium.
  • To introduce Simultaneous Immersion Mirau Interferometry (SIMI) to overcome vibration limitations of PSI.
  • To enable high-quality cell imaging for subsequent targeted irradiation experiments.

Main Methods:

  • Designed and built a custom immersion Mirau interferometric attachment for microscopy.
  • Employed phase-shifting interferometry (PSI) principles.
  • Developed SIMI using polarization optics for simultaneous interferogram acquisition, spatially separating two interferograms.

Main Results:

  • IMI and SIMI successfully imaged live and fixed cells.
  • The custom attachment ensured identical optical paths in test and reference arms.
  • SIMI effectively eliminated vibration-induced artifacts, producing high-quality images.

Conclusions:

  • IMI and SIMI are effective label-free imaging techniques for cell biology.
  • The developed system provides sufficient image quality for targeted cellular irradiation.
  • SIMI represents a significant advancement in interferometric microscopy for live-cell studies.