Wood Zachary A, Poole Leslie B, Karplus P Andrew
Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97333, USA.
Science. 2003 Apr 25;300(5619):650-3. doi: 10.1126/science.1080405.
Eukaryotic 2-Cys peroxiredoxins (2-Cys Prxs) not only act as antioxidants, but also appear to regulate hydrogen peroxide-mediated signal transduction. We show that bacterial 2-Cys Prxs are much less sensitive to oxidative inactivation than are eukaryotic 2-Cys Prxs. By identifying two sequence motifs unique to the sensitive 2-Cys Prxs and comparing the crystal structure of a bacterial 2-Cys Prx at 2.2 angstrom resolution with other Prx structures, we define the structural origins of sensitivity. We suggest this adaptation allows 2-Cys Prxs to act as floodgates, keeping resting levels of hydrogen peroxide low, while permitting higher levels during signal transduction.
真核生物双半胱氨酸过氧化物酶(2-Cys Prxs)不仅作为抗氧化剂发挥作用,而且似乎还能调节过氧化氢介导的信号转导。我们发现,细菌双半胱氨酸过氧化物酶对氧化失活的敏感性远低于真核生物双半胱氨酸过氧化物酶。通过识别敏感双半胱氨酸过氧化物酶特有的两个序列基序,并将一种细菌双半胱氨酸过氧化物酶在2.2埃分辨率下的晶体结构与其他过氧化物酶结构进行比较,我们确定了敏感性的结构根源。我们认为,这种适应性使双半胱氨酸过氧化物酶能够充当闸门,使过氧化氢的静息水平保持在较低水平,同时在信号转导期间允许更高的水平。