Optical single-channel recordings reveal correlation between lateral protein diffusion and channel activity of TOM

Electrode-free monitoring and correlation of lateral mobility with single channel activity indicates that mitochondrial β-barrel protein import pores may be mechanosensitive

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High-resolution imaging techniques have shown that many ion channels are not static, but are subject to highly dynamic processes that include transient association of pore-forming and auxiliary subunits, lateral diffusion and clustering with other proteins, which in turn affects their function1-3. However, the link between lateral diffusion and function is poorly understood.

In this study, we used a novel electrode-free optical model system4 to simultaneously monitor and subsequently correlate lateral mobility and single channel activity of a multisubunit membrane protein complex (TOM-CC, also known as the general protein import pore of the mitochondria5-9)  in membranes resting on ultrathin hydrogel films. This optical approach relies on Ca2+-ion flux through individual channels, which is measured by observing the fluorescence emission of a Ca2+-sensitive dye in close proximity to the membrane using total interference reflection fluorescence (TIRF) microscopy. In contrast to classical approaches of single-molecule tracking, no fluorescent fusion proteins or labels, which might interfere with lateral movement and function in the membrane, are required. Possible changes in ion flux associated with protein conformational changes are only caused by thermal motion of the protein and possible interactions with the hydrogel underlying the membrane.

Optical single-molecule tracking and channel activity sensing of TOM-CC in supported lipid membranes. 

We found that freely diffusing TOM-CC molecules stall when interacting with structures adjacent to the membrane, ostensibly due to interaction between its extended polar domains and the supporting hydrogel film. Surprisingly, however, and concomitantly with suspension of movement, TOM-CC changes reversibly from an active (fully light, SH) to a weakly active (medium light, SI) and inactive (dark, SL) channel state. The strong temporal correlation between lateral mobility and ion permeability suggests that TOM-CC channel gating is highly sensitive to molecular confinement and the mode of lateral diffusion. What causes the transitions between the open and the closed conformations of the two TOM-CC pores? What is acting as the “light-intensity-switch”?

Taken alongside recent cryoelectron microscopy of the TOM-CC5-9, we argue that the two Tom22 subunits of TOM-CC can force the two pore-forming β-barrel Tom40 subunits to undergo a conformational change that leads to channel closure, and that this dynamic effect represents a new functionality of TOM-CC. It will be interesting to study as to whether the mechanostimulated conformational change of the TOM-CC observed in vitro can be confirmed in intact mitochondria, where mechanosensitive interactions with components of the mitochondrial inner membrane are of physiological importance.  In this context, it might also be interesting to visualize different Tom22-dependent conformations of TOM-CC using cryo-EM, and to perform single-molecule FRET experiments to study the dynamics of TOM-CC conformers. From a general perspective, to the best of our knowledge, we believe that this may be the first demonstration of mechanoregulation of a β-barrel membrane protein complex and the causal effect of lateral diffusion. So far, mechanosensitivity has only be reported for α-helical proteins10-12.

We believe that the experimental approach we have used can be readily applied to other mechanosensitive channels where the lateral mobility, e.g. free, restricted or directed diffusion, of integral and peripheral membrane proteins is an important factor in the organisation and function of biological membranes and their components. Our study also underlies the importance of the bottom-up approach, using reconstituted systems, to understand interactions in complex physiological environments. 

Full text:

Wang, S., Findeisen, L., Leptihn, S., Wallace, M.I., Hörning, M. & Nussberger, S. Spatiotemporal stop-and-go dynamics of the mitochondrial TOM core complex correlates with channel activity, Communications Biology, DOI: 10.1038/s42003-022-03419-4 (2022).

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Stephan Nussberger

Biophysics Department, University of Stuttgart