Abstract

Scanning ion conductance microscopy (SICM) is a super-resolution live imaging technique that uses a glass nanopipette as an imaging probe to produce three-dimensional (3D) images of cell surface. SICM can be used to analyze cell morphology at nanoscale, follow membrane dynamics, precisely position an imaging nanopipette close to a structure of interest, and use it to obtain ion channel recordings or locally apply stimuli or drugs. Practical implementations of these SICM advantages, however, are often complicated due to the limitations of currently available SICM systems that inherited their design from other scanning probe microscopes in which the scan assembly is placed right above the specimen. Such arrangement makes the setting of optimal illumination necessary for phase contrast or the use of high magnification upright optics difficult. Here, we describe the designs that allow mounting SICM scan head on a standard patch-clamp micromanipulator and imaging the sample at an adjustable approach angle. This angle could be as shallow as the approach angle of a patch-clamp pipette between a water immersion objective and the specimen. Using this angular approach SICM, we obtained topographical images of cells grown on nontransparent nanoneedle arrays, of islets of Langerhans, and of hippocampal neurons under upright optical microscope. We also imaged previously inaccessible areas of cells such as the side surfaces of the hair cell stereocilia and the intercalated disks of isolated cardiac myocytes, and performed targeted patch-clamp recordings from the latter. Thus, our new, to our knowledge, angular approach SICM allows imaging of living cells on nontransparent substrates and a seamless integration with most patch-clamp setups on either inverted or upright microscopes, which would facilitate research in cell biophysics and physiology.

Highlights

  • Monitoring molecular phenomena at precisely defined cellular locations, as opposed to the entire cell or the bulk of tissue, has become essential for understanding cellular mechanisms

  • We have built a Hopping probe ion conductance microscopy (HPICM) with an adjustable nanopipette approach angle that can be integrated into any patch-clamp setup, including the setups with an upright optical microscope (Fig. 1)

  • High-resolution HPICM scanning was performed by a three-dimensional (3D) piezo actuator assembly mounted on a PatchStar micromanipulator (Scientifica, Uckfield, UK)

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Summary

Introduction

Monitoring molecular phenomena at precisely defined cellular locations, as opposed to the entire cell or the bulk of tissue, has become essential for understanding cellular mechanisms. 2252 Biophysical Journal 110, 2252–2265, May 24, 2016 reconstruction microscopy [3], structured illumination microscopy [4], stimulated emission depletion microscopy [5], or pulsed two-photon stimulated emission depletion microscopy that allows high resolution imaging deep into the tissues [6] Implementations of these techniques for imaging of living cells are still limited, because of light-induced cell damage [7,8]. They all require fluorescent tags attached to the proteins or lipids, showing nothing but structures of interest. A combination of fluorescence confocal microscopy (FCM) and confocal reflection microscopy was successfully used

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