Temperature adaptation of glutathione S-transferase P1-1 -: A case for homotropic regulation of substrate binding

被引:41
作者
Caccuri, AM
Antonini, G
Ascenzi, P
Nicotra, M
Nuccetelli, M
Mazzetti, AP
Federici, G
Lo Bello, M
Ricci, G
机构
[1] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
[2] Univ Aquila, Dept Basic & Appl Biol, I-67100 Laquila, Italy
[3] Univ Rome La Sapienza, Dept Biochem Sci A Rossi Fanelli, I-00185 Rome, Italy
[4] IRCCS Bambin Gesu, Osped Pediat, I-00165 Rome, Italy
[5] Univ Rome Tre, Dept Biol, I-00146 Rome, Italy
关键词
D O I
10.1074/jbc.274.27.19276
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human glutathione S-transferase P1-1 (GST P1-1) is a homodimeric enzyme expressed in several organs as well as in the upper layers of epidermis, playing a role against carcinogenic and toxic compounds. A sophisticated mechanism of temperature adaptation has been developed by this enzyme. In fact, above 35 degrees C, glutathione (GSH) binding to GST P1-1 displays positive cooperativity, whereas negative cooperativity occurs below 25 degrees C. This binding mechanism minimizes changes of GSH affinity for GST P1-1 because of temperature fluctuation. This is a likely advantage for epithelial skin cells, which are naturally exposed to temperature variation and, incidentally, to carcinogenic compounds, always needing efficient detoxifying systems. As a whole, GST P1-1 represents the first enzyme which displays a temperature-dependent homotropic regulation of substrate (e.g. GSH) binding.
引用
收藏
页码:19276 / 19280
页数:5
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