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bioRxiv · 10.1101/2023.06.13.544749

Predicting the placement of biomolecular structures on AFM substrates based on electrostatic interactions

Amyot, R.·Kodera, N.·Flechsig, H.
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Abstract

Atomic force microscopy (AFM) and high-speed AFM allow direct observation of biomolecular structures and their functional dynamics. Based on scanning the molecular surface of a sample deposited on a supporting substrate by a probing tip, topographic images of its dynamic shape are obtained. Critical to successful AFM observations is a balance between immobilization of the sample while avoiding too strong perturbations of its functional conformational dynamics. Since the sample placement on the supporting substrate cannot be directly controlled in experiments, the relative orientation is a priori unknown, and, due to limitations in the spatial resolution of images, difficult to infer from a posteriori analysis. We present a method to predict the macromolecular placement of samples based on electrostatic interactions with the AFM substrate and demonstrate applications to HS-AFM observations of the Cas9 endonuclease, an aptamer-protein complex, and the ClpB molecular chaperone. The model also allows predictions of imaging stability under tip-scanning. We implemented the developed method within the freely available BioAFMviewer software package. Therefore, predictions based on available structural data can be made even prior to an actual experiment.

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Amyot, R., Kodera, N., Flechsig, H.. 2023-06-14. Predicting the placement of biomolecular structures on AFM substrates based on electrostatic interactions. https://doi.org/10.1101/2023.06.13.544749

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