Structures of human Malic Enzyme 3

Grell, T. A. J.; Mason, M.; Thompson, A. A.; Gomez-Tamayo, J. C.; Riley, D.; Wagner, M. V.; Steele, R.; Ortiz-Meoz, R. F.; Wadia, J.; Shaffer, P. L.; Tresadern, G.; Sharma, S.; Yu, X.

doi:10.1101/2022.08.25.505315

bioRxiv · 10.1101/2022.08.25.505315

Structures of human Malic Enzyme 3

Grell, T. A. J.·Mason, M.·Thompson, A. A.·Gomez-Tamayo, J. C.·Riley, D.·Wagner, M. V.·Steele, R.·Ortiz-Meoz, R. F.·Wadia, J.·Shaffer, P. L.·Tresadern, G.·Sharma, S.·Yu, X.

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Abstract

Malic enzymes (ME1, ME2, and ME3) are involved in cellular energy regulation, redox homeostasis, and biosynthetic processes, through the production of pyruvate and reducing agent NAD(P)H. Recent studies have implicated the third and least well-characterized isoform, mitochondrial NADP+-dependent malic enzyme 3 (ME3), as a therapeutic target for pancreatic cancers. Here, we utilized an integrated structure approach to capture the structures of ME3 in various ligand binding states. ME3 exists as a stable tetramer and its dynamic Domain C is critical for activity. Catalytic assay results reveal that ME3 is a non-allosteric enzyme and does not require modulators for activity while structural analysis suggests that the inner stability of ME3 domain A relative to ME2 disables allostery in ME3. With structural information available for all three malic enzymes, the foundation has been laid to understand the structural and biochemical differences of these enzymes and could aid in the development of specific malic enzyme small molecule drugs.

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Grell, T. A. J., Mason, M., Thompson, A. A., Gomez-Tamayo, J. C., Riley, D., Wagner, M. V., Steele, R., Ortiz-Meoz, R. F., Wadia, J., Shaffer, P. L., Tresadern, G., Sharma, S., Yu, X.. 2022-08-25. Structures of human Malic Enzyme 3. https://doi.org/10.1101/2022.08.25.505315

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