Petros Amy K, Shaner Sarah E, Costello Alison L, Tierney David L, Gibney Brian R
Department of Chemistry, Columbia University, New York, NY 10027, USA.
Inorg Chem. 2004 Aug 9;43(16):4793-5. doi: 10.1021/ic0497679.
l-Penicillamine (Pen) has been investigated as a ligand for metalloprotein design by examining the binding of Co(II) to the sequence NH(2)-KL(Pen)EGG.(Pen)IG(Pen)GA(Pen).GGW-CONH(2). For comparison, we have studied Co(II) binding to the analogous sequence with Cys ligands, the ferredoxin maquette ligand IGA that was originally designed to bind a [4Fe-4S] cluster. The Co(II) affinity and UV-vis spectroscopic properties of IGA indicate formation of a pseudotetrahedral tetrathiolate ligated Co(II). In contrast, IGA-Pen showed formation of a pseudotetrahedral complex with Co(II) bound by three Pen ligands and an exogenous H(2)O. EXAFS data on both Co(II) complexes confirms not only the proposed primary coordination spheres but also shows six Co(II)-C(beta) methyl group distances in Co(II)-IGA-Pen. These results demonstrate that ligand sterics in simple peptides can be designed to provide asymmetric coordination spheres such as those commonly observed in natural metalloproteins.
通过研究钴(II)与序列NH(2)-KL(青霉胺)EGG.(青霉胺)IG(青霉胺)GA(青霉胺).GGW-CONH(2)的结合情况,已对左旋青霉胺(Pen)作为金属蛋白设计配体进行了研究。为作比较,我们研究了钴(II)与具有半胱氨酸配体的类似序列的结合情况,即最初设计用于结合[4Fe-4S]簇的铁氧化还原蛋白模型配体IGA。IGA的钴(II)亲和力和紫外可见光谱性质表明形成了一个假四面体四硫醇盐配位的钴(II)。相比之下,IGA-青霉胺显示形成了一个假四面体配合物,其中钴(II)由三个青霉胺配体和一个外源水分子配位。关于这两种钴(II)配合物的扩展X射线吸收精细结构(EXAFS)数据不仅证实了所提出的初级配位球,而且还显示了钴(II)-IGA-青霉胺中六个钴(II)-C(β)甲基基团的距离。这些结果表明,简单肽中的配体空间结构可被设计成提供不对称配位球,就像在天然金属蛋白中常见的那样。