Pınar GÜLLER

40522

Bazı fenolik bileşiklerle glutatyon s-transferaz ve glutatyon redüktaz inhibisyonu: in vitro ve in silico analiz

Glutatyon S-transferazlar (GSTs) ve Glutatyon redüktaz (GR) aktivitelerinin kanser hücresinde arttığı ve çoklu ilaç direncine (MDR) sebep olarak kanserin ilerlemesine katkıda bulunduğu belirlenmiştir. Glutatyon redüktaz okside glutatyon (GSSG) ile indirgenmiş nikotinamid adenin dinükleotid fosfat (NADPH) arasında elektron transferini katalize eder. Bu reaksiyon sonucu oluşan redükte glutatyon (GSH) GSTs katalizliğinde çeşitli ksenobiyotiklerin elektrofilik merkezine saldırarak detoksifiye eder. Kanser hücrelerinde antikanser ilaçların artan GST ve GR ekspresyonu ile detoksifikasyonu bu ilaçların etkinliğini azaltır. Bu nedenle kanser tedavilerinde GST ve GR inhibisyonu önemli bir yaklaşımdır. Bu çalışmada, insan eritrositlerinden GR izolasyonu 2',5'-ADP Sepharose 4B afinite kromatografisi yöntemiyle 16,912 EÜ/mg protein spesifik aktiviteyle, GST izolasyonu ise Glutatyon Agaroz afinite kromatografisi yöntemiyle 4,88 EÜ/mg protein spesifik aktiviteyle gerçekleştirilmiştir. Enzimlerin izolasyonundan sonra vanilin, epikatekin ve katekinin aktiviteler üzerine inhibisyon etkisi incelenmiştir. Her üç madde de GST’yi inhibe etmezken, vanilin ve epikatekinin GR’yi sırasıyla 86.25 µM ve 345 µM IC50 değerleriyle inhibe ettiği belirlenmiştir. İnhibisyon mekanizmasının aydınlatılması ise AutoDock programı kullanılarak moleküler yerleştirme çalışmaları ile gerçekleştirilmiştir.
Anahtar Kelimeler:

Glutatyon, vanilin, epikatekin, katekin, inhibisyon, moleküler yerleştirme

Some phenolic compounds as inhibitors of glutathione s-transferase and glutathione reductase: an in vitro and in silico analysis

It has been determined that Glutathione S-transferases (GSTs) and Glutathione reductase (GR) activities increase in cancer cells and contribute to the progression of cancer by causing multidrug resistance (MDR). Glutathione reductase catalyzes electron transfer between oxidized glutathione (GSSG) and nicotinamide adenine dinucleotide phosphate, reduced form, (NADPH). The reduced glutathione (GSH) formed as a result of this reaction detoxifies various xenobiotics by attacking the electrophilic center in the catalysis of GSTs. Detoxification of anticancer drugs with increased expression of GST and GR in cancer cells reduces the effectiveness of these drugs. Therefore, GST and GR inhibition is an important approach in cancer treatments. In this study, from human erythrocytes, GR was isolated by using 2',5'-ADP Sepharose 4B affinity chromatography method with 16.912 EU/mg protein specific activity, and GST was isolated by using Glutathione Agarose affinity chromatography method with 4.88 EU/mg protein specific activity. After the isolation of the enzymes, the inhibition effects of vanillin, epicatechin, and catechin on the activities were investigated. While all three substances did not inhibit GST, vanillin and epicatechin were found to inhibit GR with IC50 values of 86.25 μM and 345 μM, respectively. The elucidation of the inhibition mechanism was carried out by molecular docking studies using the AutoDock program.
Keywords:

Glutathione, vanillin, epicatechin, catechin, inhibition, molecular docking,

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Ata-Kimya Dergisi-Cover
  • Başlangıç: 2021
  • Yayıncı: Atatürk Üniversitesi
Arşiv
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Bazı fenolik bileşiklerle glutatyon s-transferaz ve glutatyon redüktaz inhibisyonu: in vitro ve in silico analiz

Pınar GÜLLER

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