Inhibition Effect of Eosin Y on Carbonic Anhydrase (CA) I and II Isoenzymes Purified from Human Erythrocytes
Öz
All cells produce carbon dioxide (CO2), which is released as a result of metabolism and must be removed from the body. A large part of this CO2 is converted to bicarbonate by the carbonic anhydrase (CA) enzyme in erythrocytes and is discarded from the body. So, CA has a vital role in red blood cells. In addition to, CA involved in many other pathological and physiological processes and it was determined that the inhibitors of CA were effective in the treatment and diagnosis of many diseases particularly glaucoma. Considering the importance of the CA's inhibitors, in this study it was intended to research the inhibition effects of Eosin Y on CA I and CA II isoenzymes activity purified from human erythrocytes. Eosin Y is a dye molecule commonly used in histological and medical applications. For this purpose, firstly CA I and CA II isoenzymes were purified from human erythrocytes by using Sepharose-4B-L-tyrosine-sulfanilamide affinity chromatography. Then the inhibitory effect of Eosin Y on the activity of these human erythrocyte CA I (hCA I) and CA II (hCA II) isoenzymes was investigated. It was determined that hCA I and hCA II were inhibited by Eosin Y in the millimolar range. IC50 values were found to be 3.78 mM for hCA I and 2.04 mM for hCA II and Ki values were determined as 9.65±0.968 mM and 7.52±2.88 mM for hCA I and hCA II, respectively. In conclusion, it is hoped that the results obtained in this study may be beneficial in the development of new CA inhibitors which may be drug candidates.
Anahtar Kelimeler
Kaynakça
- Aggarwal M, Kondeti B, McKenna R, 2013. Anticonvulsant/antiepileptic carbonic anhydrase inhibitors: a patent review. Expert Opinion on Therapeutic Patents, 23 (6): 717-724.
- Aksu K, Nar M, Tanç M, Vullo D, Gulcin I, Göksu F, Tümer F, Supuran CT, 2013. The synthesis of sulfamide analogues of dopamine related compounds and their carbonic anhydrase inhibitory properties. Biorganic Medicinal Chemistry, 21 (11): 2925-2931.
- Alım Z, Kilinc N, Sengul B, Beydemir S, 2015. Some Anti-Inflammatory Agents Inhibit Esterase Activities of Human Carbonic Anhydrase Isoforms i and II: An in Vitro Study. Chemical Biology and Drug Design, 86 (4): 857-863.
- Alım Z, 2018. 1H-indazole molecules reduced the activity of human erythrocytes carbonic anhydrase I and II isoenzymes. Journal of Biochemical and Molecular Toxicology, 32 (9): e22194. Alterio V, Di Fiore A, D'Ambrosio K, Supuran CT, De Simone G, 2012. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms. Chemical Reviews, 112 (8): 4421-4468.
- Aslan HE, Demir Y, Özaslan MS, Türkan F, Beydemir Ş, Küfrevioğlu ÖI. 2019. The behavior of some chalcones on acetylcholinesterase and carbonic anhydrase activity. Drug and Chemical Toxicology, 42(6):634-640.
- Benej M, Pastorekova S, Pastorek J, 2014. Carbonic anhydrase IX: regulation and role in cancer. Subcellular Biochemistry, 75: 199-219.
- Bradford MM, 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical biochemistry, 72 (1-2): 248–251.
- Buzas GM, Supuran CT, 2016. The history and rationale of using carbonic anhydrase inhibitors in the treatment of peptic ulcers. In memoriam Ioan Puşcaş (1932-2015). Journal of Enzyme Inhibition Medicinal Chemistry, 31 (4): 527-533.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Kimya Mühendisliği
Bölüm
Araştırma Makalesi
Yazarlar
Zuhal Alım
*
0000-0003-1977-1756
Türkiye
Yayımlanma Tarihi
1 Mart 2020
Gönderilme Tarihi
18 Temmuz 2019
Kabul Tarihi
16 Eylül 2019
Yayımlandığı Sayı
Yıl 2020 Cilt: 10 Sayı: 1
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