Pippel Jan, Kuettner E Bartholomeus, Ulbricht David, Daberger Jan, Schultz Stephan, Heiker John T, Sträter Norbert
Biol Chem. 2016 Jan 1;397(2):111-23. doi: 10.1515/hsz-2015-0229.
The adipokine vaspin (serpinA12) is mainly expressed in white adipose tissue and exhibits various beneficial effects on obesity-related processes. Kallikrein 7 is the only known target protease of vaspin and is inhibited by the classical serpin inhibitory mechanism involving a cleavage of the reactive center loop between P1 (M378) and P1' (E379). Here, we present the X-ray structure of vaspin, cleaved between M378 and E379. We provide a comprehensive analysis of differences between the uncleaved and cleaved forms in the shutter, breach, and hinge regions with relation to common molecular features underlying the serpin inhibitory mode. Furthermore, we point out differences towards other serpins and provide novel data underlining the remarkable stability of vaspin. We speculate that the previously reported FKGx1Wx2x3 motif in the breach region may play a decisive role in determining the reactive center loop configuration in the native vaspin state and might contribute to the high thermostability of vaspin. Thus, this structure may provide a basis for future mutational studies.
脂肪因子内脏脂肪素(丝氨酸蛋白酶抑制剂A12)主要在白色脂肪组织中表达,并对肥胖相关过程表现出多种有益作用。激肽释放酶7是内脏脂肪素唯一已知的靶蛋白酶,它通过经典的丝氨酸蛋白酶抑制剂抑制机制被抑制,该机制涉及P1(M378)和P1'(E379)之间反应中心环的切割。在此,我们展示了在M378和E379之间切割后的内脏脂肪素的X射线结构。我们全面分析了未切割和切割形式在快门、裂隙和铰链区域的差异,以及与丝氨酸蛋白酶抑制剂抑制模式潜在的共同分子特征的关系。此外,我们指出了与其他丝氨酸蛋白酶抑制剂的差异,并提供了新的数据强调内脏脂肪素显著的稳定性。我们推测,先前报道的裂隙区域中的FKGx1Wx2x3基序可能在决定天然内脏脂肪素状态下反应中心环的构象中起决定性作用,并且可能有助于内脏脂肪素的高热稳定性。因此,该结构可能为未来的突变研究提供基础。