Protein disulfide isomerase and glutathione are alternative substrates in the one Cys catalytic cycle of glutathione peroxidase 7

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• 作者：Valentina Bosello-Travain^a ; Marcus Conrad^b ; Giorgio Cozza^c ; Alessandro Negro^c ; Silvia Quartesan^a ; Monica Rossetto^a ; Antonella Roveri^a ; Stefano Toppo^a ; Fulvio Ursini^a ; Mattia Zaccarin^a ; Matilde Maiorino^a ; ^{matilde.maiorino@unipd.it}
• 关键词：CysGPxs ; subfamily of glutathione peroxidases containing a Cys redox center ; 1CysGPx ; a glutathione peroxidase containing the CP only ; 2CysGPxs ; glutathione peroxidases containing both the CP and the CR ; CP ; peroxidatic Cys ; CR ; resolving Cys ; GPx7 ; gluta
• 刊名：Biochimica et Biophysica Acta (BBA)/General Subjects
• 出版年：2013
• 出版时间：June, 2013
• 年：2013
• 卷：1830
• 期：6
• 页码：3846-3857
• 全文大小：2303 K

文摘

Background

Mammalian GPx7 is a monomeric glutathione peroxidase of the endoplasmic reticulum (ER), containing a Cys redox center (CysGPx). Although containing a peroxidatic Cys (C_P) it lacks the resolving Cys (C_R), that confers fast reactivity with thioredoxin (Trx) or related proteins to most other CysGPxs.

Methods

Reducing substrate specificity and mechanism were addressed by steady-state kinetic analysis of wild type or mutated mouse GPx7. The enzymes were heterologously expressed as a synuclein fusion to overcome limited expression. Phospholipid hydroperoxide was the oxidizing substrate. Enzyme-substrate and protein-protein interaction were analyzed by molecular docking and surface plasmon resonance analysis.

Results

Oxidation of the C_P is fast (k_+ 1 > 10³ M^? 1 s^? 1), however the rate of reduction by GSH is slow (k¡ä_+ 2 = 12.6 M^? 1 s^? 1) even though molecular docking indicates a strong GSH-GPx7 interaction. Instead, the oxidized C_P can be reduced at a fast rate by human protein disulfide isomerase (HsPDI) (k_+ 1 > 10³ M^? 1 s^? 1), but not by Trx. By surface plasmon resonance analysis, a K_D = 5.2 ¦ÌM was calculated for PDI-GPx7 complex. Participation of an alternative non-canonical C_R in the peroxidatic reaction was ruled out. Specific activity measurements in the presence of physiological reducing substrate concentration, suggest substrate competition in vivo.

Conclusions

GPx7 is an unusual CysGPx catalyzing the peroxidatic cycle by a one Cys mechanism in which GSH and PDI are alternative substrates.

General significance

In the ER, the emerging physiological role of GPx7 is oxidation of PDI, modulated by the amount of GSH.