Effects of Alzheimer's Disease Drug Candidates on Disordered Aβ42 Dissected by Comparative Markov State Analysis (CoVAMPnet)

Marques, S. M.; Kouba, P.; Legrand, A.; Sedlar, J.; Disson, L.; Planas-Iglesias, J.; Sanusi, Z.; Kunka, A.; Damborsky, J.; Pajdla, T.; Prokop, Z.; Mazurenko, S.; Sivic, J.; Bednar, D.

doi:10.1101/2023.01.06.523007

bioRxiv · 10.1101/2023.01.06.523007

Effects of Alzheimer's Disease Drug Candidates on Disordered Aβ42 Dissected by Comparative Markov State Analysis (CoVAMPnet)

Marques, S. M.·Kouba, P.·Legrand, A.·Sedlar, J.·Disson, L.·Planas-Iglesias, J.·Sanusi, Z.·Kunka, A.·Damborsky, J.·Pajdla, T.·Prokop, Z.·Mazurenko, S.·Sivic, J.·Bednar, D.

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Abstract

Computational study of the effect of drug candidates on intrinsically disordered biomolecules is challenging due to their vast and complex conformational space. Here we developed a Comparative Markov State Analysis (CoVAMPnet) framework to quantify changes in the conformational distribution and dynamics of a disordered biomolecule in the presence and absence of small organic drug candidate molecules. First, molecular dynamics trajectories are generated using enhanced sampling, in the presence and absence of small molecule drug candidates, and ensembles of soft Markov state models (MSMs) are learned for each system using unsupervised machine learning. Second, these ensembles of learned MSMs are aligned across different systems based on a solution to an optimal transport problem. Third, the directional importance of inter-residue distances for the assignment to different conformational states is assessed by a discriminative analysis of aggregated neural network gradients. This final step provides interpretability and biophysical context to the learned MSMs. We applied this novel computational framework to assess the effects of ongoing phase 3 therapeutics tramiprosate (TMP) and its metabolite 3-sulfopropanoic acid (SPA) on the disordered A{beta}42 peptide involved in Alzheimers disease. Based on adaptive sampling molecular dynamics and CoVAMPnet analysis, we observed that both TMP and SPA preserved more structured conformations of A{beta}42 by interacting non-specifically with charged residues. SPA impacted A{beta}42 more than TMP, protecting -helices and suppressing the formation of aggregation-prone {beta}-strands. Experimental biophysical analyses showed only mild effects of TMP/SPA on A{beta}42, and activity enhancement by the endogenous metabolization of TMP into SPA. Our data suggest that TMP/SPA may also target other biomolecules than A{beta} peptides. The CoVAMPnet method is broadly applicable to study the effects of drug candidates on the conformational behavior of intrinsically disordered biomolecules. TOC Graphic O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=109 SRC="FIGDIR/small/523007v2_ufig1.gif" ALT="Figure 1"> View larger version (46K): org.highwire.dtl.DTLVardef@13eea16org.highwire.dtl.DTLVardef@17a6bd1org.highwire.dtl.DTLVardef@3c6b33org.highwire.dtl.DTLVardef@a20444_HPS_FORMAT_FIGEXP M_FIG C_FIG

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Marques, S. M., Kouba, P., Legrand, A., Sedlar, J., Disson, L., Planas-Iglesias, J., Sanusi, Z., Kunka, A., Damborsky, J., Pajdla, T., Prokop, Z., Mazurenko, S., Sivic, J., Bednar, D.. 2023-01-06. Effects of Alzheimer's Disease Drug Candidates on Disordered Aβ42 Dissected by Comparative Markov State Analysis (CoVAMPnet). https://doi.org/10.1101/2023.01.06.523007

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