Biology:Small copper carrier

From HandWiki

Small copper carrier or SCC is a small molecule that transports copper in urine. It is excreted in the kidneys in humans or mice where the liver is unable to excrete excess copper in bile. This happens in Wilson’s disease where the presence of copper in urine is a diagnostic.[1] It was discovered by Lawrence Wilson Gray and Svetlana Lutsenko.[2] The molecule is 2 kDa. Its exact nature is not yet known but is presumed to be a peptide.[3] The same peptide also appears in blood and urine of many different mammals. Its copper free molecular weight is 1329.5.[4] In neutral conditions the small copper carrier molecule has a negative charge. Copper is bound to the carrier via oxygen and nitrogen (O or N).[5]

References

  1. ↑ "Copper's previously unknown exit strategy". 13 July 2012. http://medicalxpress.com/news/2012-07-copper-previously-unknown-exit-strategy.html. 
  2. ↑ Gray, Wilson Lawrence. "Mechanisms of Homeostatic Control of Copper in Tissues". Database for Research Grants. http://www.researchgrantdatabase.com/g/5F31DK084730-03/. 
  3. ↑ Gray, Lawrence; Fangyu Peng; Shannon A. Molloy; Venkata S. Pendyala; Abigael Muchenditsi; Otto Muzik; Jaekwon Lee; Jack H. Kaplan et al. (2012). "Urinary Copper Elevation in a Mouse Model of Wilson's Disease Is a Regulated Process to Specifically Decrease the Hepatic Copper Load". PLOS ONE 7 (6): e38327. doi:10.1371/journal.pone.0038327. ISSN 1932-6203. PMID 22802922. Bibcode: 2012PLoSO...738327G. 
  4. ↑ Miguel Tellez; Travis Alsky; Matthew Dalphin; Stephen Flynn; Arturo Munoz; Denise Ibarra; Helen Truong; Maria C Linder et al. (April 2016). "Purification and characterization of a small copper carrier found in mammalian blood plasma and in the urine of mice and dogs with copper overload". FASEB Journal 30 (1). doi:10.1096/fasebj.30.1_supplement.1026.2. 
  5. ↑ Linder, Maria C. (13 July 2020). "Copper Homeostasis in Mammals, with Emphasis on Secretion and Excretion. A Review". International Journal of Molecular Sciences 21 (14): 4932. doi:10.3390/ijms21144932. PMID 32668621. 



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