Shape, membrane morphology, and morphodynamic response of metabolically active human mitochondria revealed by scanning ion conductance microscopy

• Eric Lieberwirth,
• Anja Schaeper,
• Regina Lange,
• Ingo Barke,
• Simone Baltrusch and
• Sylvia Speller

Beilstein J. Nanotechnol. 2025, 16, 951–967, doi:10.3762/bjnano.16.73

• . Consequently, the outer membrane, which separates the mitochondrion from the cytoplasm, has become a focus of investigation. We analysed metabolically active mitochondria from HeLa cells using scanning ion conductance microscopy to generate nanoscopically resolved, three-dimensional topographies. Our

• local environment. The similarities between the nanopipette in the measurement setup and the microtubules in the cellular context are discussed as the basis for the hypothesis. Keywords: HeLa; metabolically active; mitochondria; morphodynamics; scanning ion conductance microscopy; Introduction

• study of metabolically active organelles [26]. Scanning ion conductance microscopy (SICM) enables three-dimensional visualisation of living cells in their native state [27]. Pioneered by Hansma et al. [28], the method has been continuously refined since the 1990s [27][29][30]. SICM utilises a

Two dynamic modes to streamline challenging atomic force microscopy measurements

• Alexei G. Temiryazev,
• Andrey V. Krayev and
• Marina P. Temiryazeva

Beilstein J. Nanotechnol. 2021, 12, 1226–1236, doi:10.3762/bjnano.12.90

• parachuting and sticking (Figure 2a). Figure 2a and Figure 2b show the top of a micropipette, which is a probe in scanning ion conductance microscopy [25]. From Figure 2b, we can estimate that the diameter of the intact micropipette at its most protruding part is about 100 nm. To do this, we need to make a

The nanomorphology of cell surfaces of adhered osteoblasts

• Christian Voelkner,
• Mirco Wendt,
• Regina Lange,
• Max Ulbrich,
• Martina Gruening,
• Susanne Staehlke,
• Barbara Nebe,
• Ingo Barke and
• Sylvia Speller

Beilstein J. Nanotechnol. 2021, 12, 242–256, doi:10.3762/bjnano.12.20

• present a comprehensive characterization of the 3D nanomorphology of living, as well as fixed, osteoblastic cells using scanning ion conductance microscopy (SICM), which is a nanoprobing method that largely avoids mechanical perturbations. Dynamic ruffles are observed, manifesting themselves in

• capability of apical membrane features and fluctuation dynamics in aiding the assessment of adhesion and migration properties on a single-cell basis. Keywords: cell adhesion; membrane fluctuations; osteoblast; plasma membrane nanomorphology; scanning ion conductance microscopy (SICM); Introduction

• remain obscure. A localized ion current flowing through a nanopipette probe represents a suitable non-invasive interaction, which is exploited in scanning ion conductance microscopy (SICM) [19][20][21]. SICM is well suited to probe soft and responsive surfaces, such as those of living cells. The applied

Scanning probe microscopy and related methods

• Ernst Meyer

Beilstein J. Nanotechnol. 2010, 1, 155–157, doi:10.3762/bjnano.1.18

• resonance-STM, SICM: Scanning ion conductance microscopy, CAFM: Conductive AFM.