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麩胱甘肽硫轉換酶

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麩胱甘肽硫轉換酶 cGSTM1-1 與不同受質形 成複合體之結構及功能研究

研究小雞肝臟的 mu 類麩胱甘肽硫轉換酶 (glutathione S-trans ferase) cGSTM1-1 ,與麩胱甘肽 (GSH) 接合上 1,2-epoxy-3- (p-nitrophenoxy) propane (EPNP) 形成的 GS-EPNP 作為受質 形成複合體,進行 X 光結晶學研究以決定出結構,並修正 解析度至 2.8 A 。其結構可解釋 cGSTM1-1 中 epoxidase 活 性的因素。此複合體在結晶學上所定義之不對稱單位中含兩 個 dimer ,依序定為 AB 及 CD 。在 dimer AB 中, EPNP 的部分朝向 Arg107 及 Gln165 且形成氫鍵。而在 dimer CD 中, EPNP 的部分則伸出至由連接 b1 及 a1 的 loop 和部分 C 端殘基銜接形成的疏水性區,且 EPNP 上的 phenoxyl rin g 與 Trp209 側鏈形成強烈的環堆疊作用。我們因而推論出 此兩種不同構形代表的 EPNP 分別接近其啟始及最終催化反 應階段,此結論與 cGSTM1-1 突變株的酵素動力學實驗結果 相互印證。

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Structure and Functional Study of Glutathione S-tr ansferase cGSTM1-1 Complexed with Various Sub

strates

We elucidated the three-dimensional structure of mu-class glutathione S-tr

ansferase cGSTM1-1 co-crystallized with the glutathionyl conjugated 1,2-e

poxy-3-(p-nitrophenoxy)propane (GS-EPNP) at 2.8A resolution. The prod

uct found in the active site was 1-hydroxy-2-(S-glutathionyl)-3- (p-nitroph

enoxy) propane, instead of the conventionally decided 2-hydroxy isomer. T

he structure can explain the epoxidase activity of cGSTM1-1 to the substra

tes. The EPNP moiety orients towards Arg107(α4 helix), and Gln165(α6 h

elix ) in dimer AB and protrudes into a hydrophobic region formed by the l

oop connectingβ1 and α1 and part of the C-terminal tail in dimer CD. The

phenoxyl ring forms strong ring stacking with the Trp209 side-chain in di

mer CD. We hypothesize that these two conformations represent the EPNP

moiety close to the initial and final stages of the reaction mechanism, respe

ctively. And the conclusion was confirmed with the report of the mutagene

sis and kinetic studies of cGSTM1-1.

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