SLC31 family of copper transporters
SLC31 family members, alongside the Cu-ATPases are involved in the regulation of cellular copper levels. The CTR1 transporter is a cell-surface transporter to allow monovalent copper accumulation into cells, while CTR2 appears to be a vacuolar/vesicular transporter [4]. Functional copper transporters appear to be trimeric with each subunit having three TM regions and an extracellular N-terminus. CTR1 is considered to be a higher affinity copper transporter compared to CTR2. The stoichiometry of copper accumulation is unclear, but appears to be energy-independent [3].
Unless otherwise stated all data refer to the human proteins. Gene information is provided for human (Hs), mouse (Mm) and rat (Rn).
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Copper transporter 1 (SLC31A1) Show »« Hide
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Copper transporter 2 (SLC31A2) Show »« Hide
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De Feo, CJ; Aller, SG; Unger, VM. (2007) A structural perspective on copper uptake in eukaryotes. Biometals, 20 (3-4): 705-16. [PMID:17211682]
Howell, SB; Safaei, R; Larson, CA; Sailor, MJ. (2010) Copper transporters and the cellular pharmacology of the platinum-containing cancer drugs. Mol. Pharmacol., 77 (6): 887-94. [PMID:20159940]
Maryon, EB; Molloy, SA; Zimnicka, AM; Kaplan, JH. (2007) Copper entry into human cells: progress and unanswered questions. Biometals, 20 (3-4): 355-64. [PMID:17211679]
Nose, Y; Rees, EM; Thiele, DJ. (2006) Structure of the Ctr1 copper trans'PORE'ter reveals novel architecture. Trends Biochem. Sci., 31 (11): 604-7. [PMID:16982196]
Petris, MJ. (2004) The SLC31 (Ctr) copper transporter family. Pflugers Arch., 447 (5): 752-5. [PMID:12827356]
1. Blair, BG; Larson, CA; Safaei, R; Howell, SB. (2009) Copper transporter 2 regulates the cellular accumulation and cytotoxicity of Cisplatin and Carboplatin. Clin. Cancer Res., 15 (13): 4312-21. [PMID:19509135]
2. Ishida, S; Lee, J; Thiele, DJ; Herskowitz, I. (2002) Uptake of the anticancer drug cisplatin mediated by the copper transporter Ctr1 in yeast and mammals. Proc. Natl. Acad. Sci. U.S.A., 99 (22): 14298-302. [PMID:12370430]
3. Lee, J; Peña, MM; Nose, Y; Thiele, DJ. (2002) Biochemical characterization of the human copper transporter Ctr1. J. Biol. Chem., 277 (6): 4380-7. [PMID:11734551]
4. Rees, EM; Lee, J; Thiele, DJ. (2004) Mobilization of intracellular copper stores by the ctr2 vacuolar copper transporter. J. Biol. Chem., 279 (52): 54221-9. [PMID:15494390]
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Copper accumulation through CTR1 is sensitive to silver ions, but not divalent cations [3]. The CTR1 and CTR2 transporters regulate the cellular levels of the anticancer drug cisplatin [1-2].