Cystine is the oxidized derivative of the amino acidcysteine and has the formula (SCH2CH(NH2)CO2H)2. It is a white solid that is poorly soluble in water. As a residue in proteins, cystine serves two functions: a site of redox reactions and a mechanical linkage that allows proteins to retain their three-dimensional structure.[1]
Cystine contains a disulfide bond, two amine groups, and two carboxylic acid groups. As for other amino acids, the amine and carboxylic acid groups exist in rapid equilibrium with the ammonium-carboxylate tautomer. The great majority of the literature concerns the l,l-cystine, derived from l-cysteine. Other isomers include d,d-cystine and the meso isomer d,l-cystine, neither of which is biologically significant.
Cystine is common in many foods such as eggs, meat, dairy products, and whole grains as well as skin, horns and hair. It was not recognized as being derived of proteins until it was isolated from the horn of a cow in 1899.[2] Human hair and skin contain approximately 10–14% cystine by mass.[3]
Cystine was discovered in 1810 by the English chemist William Hyde Wollaston, who called it "cystic oxide".[4][5]In 1833, the Swedish chemist Jöns Jacob Berzelius named the amino acid "cystine".[6] The Norwegian chemist Christian J. Thaulow determined, in 1838, the empirical formula of cystine.[7] In 1884, the German chemist Eugen Baumann found that when cystine was treated with a reducing agent, cystine revealed itself to be a dimer of a monomer which he named "cysteïne".[8][5]In 1899, cystine was first isolated from protein (horn tissue) by the Swedish chemist Karl A. H. Mörner (1855-1917).[9] The chemical structure of cystine was determined by synthesis in 1903 by the German chemist Emil Erlenmeyer.[10][11][12]
The history of cystine and cysteine is complicated by the dimer-monomer relationship of the two.[5] The cysteine monomer was proposed as the actual unit by Embden in 1901.
The sulfur within the structure of cysteine and cystine has been subject of historical interest.[5]In 1902, Osborne partially succeeded in analysing cystine content via lead compounds. An improved colorimetric method was developed in 1922 by Folin and Looney. An iodometric analysis method was developed by Okuda in 1925.
It is formed from the oxidation of two cysteine molecules, which results in the formation of a disulfide bond. In cell biology, cystine residues (found in proteins) only exist in non-reductive (oxidative) organelles, such as the secretory pathway (endoplasmic reticulum, Golgi apparatus, lysosomes, and vesicles) and extracellular spaces (e.g., extracellular matrix). Under reductive conditions (in the cytoplasm, nucleus, etc.) cysteine is predominant. The disulfide link is readily reduced to give the corresponding thiolcysteine. Typical thiols for this reaction are mercaptoethanol and dithiothreitol:
Because of the facility of the thiol-disulfide exchange, the nutritional benefits and sources of cystine are identical to those for the more-common cysteine. Disulfide bonds cleave more rapidly at higher temperatures.[13]
Comparison of different types of urinary crystals.
The presence of cystine in urine is often indicative of amino acid reabsorption defects. Cystinuria has been reported to occur in dogs.[14]
In humans the excretion of high levels of cystine crystals can be indicative of cystinosis, a rare genetic disease. Cystine stones account for about 1-2% of kidney stone disease in adults.[15][16]
Cystine serves as a substrate for the cystine-glutamate antiporter. This transport system, which is highly specific for cystine and glutamate, increases the concentration of cystine inside the cell. In this system, the anionic form of cystine is transported in exchange for glutamate. Cystine is quickly reduced to cysteine.[citation needed] Cysteine prodrugs, e.g. acetylcysteine, induce release of glutamate into the extracellular space.
This article is missing information about hair growth supplements. Please expand the article to include this information. Further details may exist on the talk page.(November 2022)
Cysteine supplements are sometimes marketed as anti-aging products with claims of improved skin elasticity.[citation needed] Cysteine is more easily absorbed by the body than cystine, so most supplements contain cysteine rather than cystine. N-acetyl-cysteine (NAC) is better absorbed than other cysteine or cystine supplements.
^Berzelius, J.J.; Esslinger, Me., trans. (1833). Traité de Chimie (in French). Vol. 7. Paris, France: Didot Frères. p. 424.{{cite book}}: CS1 maint: multiple names: authors list (link) From p. 424: "10. Cystine. Cette substance a été découverte dans les calculs urinaires par Wollaston, […] je me suis donc permis de changer le nom qu'avait proposé cet homme distingué." (10. Cystine. This substance was discovered in urinary calculi by Wollaston, who gave it the name of "cystic oxide" because it dissolves as much in acids as in alkalis, and it resembles, in this respect, some metallic oxides; but, in a way, the reason [that was] alleged to justify it is not valid: I have therefore taken the liberty of changing the name that this distinguished man had proposed.)
^Baumann, E. (1884). "Ueber Cystin und Cysteïn" [On cystine and cysteine]. Zeitschrift für physiologische Chemie (in German). 8: 299–305. From pp. 301-302: "Die Analyse der Substanz ergibt Werthe, welche den vom Cystin (C6H12N2S2O4) verlangten sich nähern, […] nenne ich dieses Reduktionsprodukt des Cystins: Cysteïn." (Analysis of the substance [cysteine] reveals values which approximate those [that are] required by cystine (C6H12N2S2O4), however the new base [cysteine] can clearly be recognized as a reduction product of cystine, to which the [empirical] formula C3H7NSO2, [which had] previously [been] ascribed to cystine, is [now] ascribed. In order to indicate the relationships of this substance to cystine, I name this reduction product of cystine: "cysteïne".) Note: Baumann's proposed structures for cysteine and cystine (see p.302) are incorrect: for cysteine, he proposed CH3CNH2(SH)COOH .
^Erlenmeyer's findings regarding the structure of cystine were confirmed in 1908 by Fischer and Raske. See: Fischer, Emil; Raske, Karl (1908). "Verwandlung des l-Serines in aktives natürliches Cystin" [Conversion of l-serine into [optically] active natural cystine]. Berichte der Deutschen Chemischen Gesellschaft (in German). 41: 893–897. doi:10.1002/cber.190804101169.
^Aslaksena, M.A.; Romarheima, O.H.; Storebakkena, T.; Skrede, A. (28 June 2006). "Evaluation of content and digestibility of disulfide bonds and free thiols in unextruded and extruded diets containing fish meal and soybean protein sources". Animal Feed Science and Technology. 128 (3–4): 320–330. doi:10.1016/j.anifeedsci.2005.11.008.
^Gahl, William A.; Thoene, Jess G.; Schneider, Jerry A. (2002). "Cystinosis". New England Journal of Medicine. 347 (2): 111–121. doi:10.1056/NEJMra020552. PMID12110740.
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