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The ZIP-prion connection

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Pages 317-321 | Published online: 17 May 2012

Figures & data

Figure 1. Localization, function and possible interaction of LZTs with the prion protein. (A) Cartoon depicting the reported predominant cellular localization of LIV-1 ZIP transporter (LZT) family members. Whereas more distantly related LZT metal ion transporters may preferentially associate with a variety of intracellular organelles, members of the phylogenetic subbranch of LZTs comprising ZIPs 5, 6 and 10 are predominantly observed at the plasma membrane. (B) Model of prion protein next to an LZT, depicted with its predicted PrP-like ectodomain. The interface that mediates the interaction between PrP and LZTs is as yet undefined. (C) Model of LZT-mediated cellular zinc import through passive diffusion and shedding of the PrP-like ectodomain in response to extracellular metal starvation. It should be noted that a similar endoproteolysis of a subset of LZTs can be observed in prion-infected mouse brains (unpublished dataCitation20). Panels B and C were modified from a Progress in Neurobiology articleCitation3 with permission from Elsevier.

Figure 1. Localization, function and possible interaction of LZTs with the prion protein. (A) Cartoon depicting the reported predominant cellular localization of LIV-1 ZIP transporter (LZT) family members. Whereas more distantly related LZT metal ion transporters may preferentially associate with a variety of intracellular organelles, members of the phylogenetic subbranch of LZTs comprising ZIPs 5, 6 and 10 are predominantly observed at the plasma membrane. (B) Model of prion protein next to an LZT, depicted with its predicted PrP-like ectodomain. The interface that mediates the interaction between PrP and LZTs is as yet undefined. (C) Model of LZT-mediated cellular zinc import through passive diffusion and shedding of the PrP-like ectodomain in response to extracellular metal starvation. It should be noted that a similar endoproteolysis of a subset of LZTs can be observed in prion-infected mouse brains (unpublished dataCitation20). Panels B and C were modified from a Progress in Neurobiology articleCitation3 with permission from Elsevier.

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