Combined Atomic Force Microscope and Volumetric Light Sheet System for Correlative Force and Fluorescence Mechanobiology Studies

  • E. Nelsen
  • , C. M. Hobson
  • , M. E. Kern
  • , J. P. Hsiao
  • , E. T. O’Brien
  • , T. Watanabe
  • , B. M. Condon
  • , M. Boyce
  • , S. Grinstein
  • , K. M. Hahn
  • , M. R. Falvo
  • , R. Superfine

Research output: Contribution to journalArticlepeer-review

29 Citations (Scopus)

Abstract

The central goals of mechanobiology are to understand how cells generate force and how they respond to environmental mechanical stimuli. A full picture of these processes requires high-resolution, volumetric imaging with time-correlated force measurements. Here we present an instrument that combines an open-top, single-objective light sheet fluorescence microscope with an atomic force microscope (AFM), providing simultaneous volumetric imaging with high spatiotemporal resolution and high dynamic range force capability (10 pN – 100 nN). With this system we have captured lysosome trafficking, vimentin nuclear caging, and actin dynamics on the order of one second per single-cell volume. To showcase the unique advantages of combining Line Bessel light sheet imaging with AFM, we measured the forces exerted by a macrophage during FcɣR-mediated phagocytosis while performing both sequential two-color, fixed plane and volumetric imaging of F-actin. This unique instrument allows for a myriad of novel studies investigating the coupling of cellular dynamics and mechanical forces.

Original languageEnglish
Article number8133
JournalScientific reports
Volume10
Issue number1
DOIs
Publication statusPublished - 01-12-2020
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General

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