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. 2017 Jun;74(12):2299-2318.
doi: 10.1007/s00018-017-2461-9. Epub 2017 Jan 28.

Membrane-traversing Mechanism of Thyroid Hormone Transport by Monocarboxylate Transporter 8

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Membrane-traversing Mechanism of Thyroid Hormone Transport by Monocarboxylate Transporter 8

Jonas Protze et al. Cell Mol Life Sci. .

Abstract

Monocarboxylate transporter 8 (MCT8) mediates thyroid hormone (TH) transport across the plasma membrane in many cell types. In order to better understand its mechanism, we have generated three new MCT8 homology models based on sugar transporters XylE in the intracellular opened (PDB ID: 4aj4) and the extracellular partly occluded (PDB ID: 4gby) conformations as well as FucP (PDB ID: 3o7q) and GLUT3 (PDB ID: 4zwc) in the fully extracellular opened conformation. T3-docking studies from both sides revealed interactions with His192, His415, Arg445 and Asp498 as previously identified. Selected mutations revealed further transport-sensitive positions mainly at the discontinuous transmembrane helices TMH7 and 10. Lys418 is potentially involved in neutralising the charge of the TH substrate because it can be replaced by charged, but not by uncharged, amino acids. The side chain of Thr503 was hypothesised to stabilise a helix break at TMH10 that undergoes a prominent local shift during the transport cycle. A T503V mutation accordingly affected transport. The aromatic Tyr419, the polar Ser313 and Ser314 as well as the charged Glu422 and Glu423 lining the transport channel have been studied. Based on related sugar transporters, we suggest an alternating access mechanism for MCT8 involving a series of amino acid positions previously and newly identified as critical for transport.

Keywords: MFS-transporter; Membrane proteins; Molecular modelling; Mutagenesis; Structure–function study; Thyroid hormones.

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References

    1. J Neurosci. 2009 Jul 29;29(30):9439-49 - PubMed
    1. Nature. 2015 Oct 15;526(7573):397-401 - PubMed
    1. J Mol Biol. 2006 Jul 14;360(3):586-98 - PubMed
    1. J Mol Biol. 2007 Nov 2;373(4):1006-16 - PubMed
    1. J Biol Chem. 2003 Oct 31;278(44):43489-95 - PubMed

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