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8WTW

Cryo-EM structure of noradrenaline transporter in complex with a x-MrlA analogue

Summary for 8WTW
Entry DOI10.2210/pdb8wtw/pdb
EMDB information37844
DescriptorSodium-dependent noradrenaline transporter, MrlA, CHLORIDE ION, ... (4 entities in total)
Functional Keywordsnorapinephrine transporter, mrla, structural protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight65548.61
Authors
Zhao, Y.,Hu, T.,Yu, Z. (deposition date: 2023-10-19, release date: 2024-08-07, Last modification date: 2024-10-02)
Primary citationHu, T.,Yu, Z.,Zhao, J.,Meng, Y.,Salomon, K.,Bai, Q.,Wei, Y.,Zhang, J.,Xu, S.,Dai, Q.,Yu, R.,Yang, B.,Loland, C.J.,Zhao, Y.
Transport and inhibition mechanisms of the human noradrenaline transporter.
Nature, 632:930-937, 2024
Cited by
PubMed Abstract: The noradrenaline transporter (also known as norepinephrine transporter) (NET) has a critical role in terminating noradrenergic transmission by utilizing sodium and chloride gradients to drive the reuptake of noradrenaline (also known as norepinephrine) into presynaptic neurons. It is a pharmacological target for various antidepressants and analgesic drugs. Despite decades of research, its structure and the molecular mechanisms underpinning noradrenaline transport, coupling to ion gradients and non-competitive inhibition remain unknown. Here we present high-resolution complex structures of NET in two fundamental conformations: in the apo state, and bound to the substrate noradrenaline, an analogue of the χ-conotoxin MrlA (χ-MrlA), bupropion or ziprasidone. The noradrenaline-bound structure clearly demonstrates the binding modes of noradrenaline. The coordination of Na and Cl undergoes notable alterations during conformational changes. Analysis of the structure of NET bound to χ-MrlA provides insight into how conotoxin binds allosterically and inhibits NET. Additionally, bupropion and ziprasidone stabilize NET in its inward-facing state, but they have distinct binding pockets. These structures define the mechanisms governing neurotransmitter transport and non-competitive inhibition in NET, providing a blueprint for future drug design.
PubMed: 39085602
DOI: 10.1038/s41586-024-07638-z
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.8 Å)
Structure validation

227344

건을2024-11-13부터공개중

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