Zhang Chun-Mei, Christian Thomas, Newberry Kate J, Perona John J, Hou Ya-Ming
Department of Biochemistry and Molecular Pharmacology, Thomas Jefferson University, 233 S 10th Street, BLSB 222, Philadelphia, PA 19107, USA.
J Mol Biol. 2003 Apr 11;327(5):911-7. doi: 10.1016/s0022-2836(03)00241-9.
Escherichia coli cysteinyl-tRNA synthetase (CysRS) achieves a high level of amino acid specificity without an editing reaction. The crystal structure of CysRS bound to substrate cysteine suggested that direct thiol coordination to a tightly bound zinc ion at the base of the active site is the primary determinant of selectivity against non-cognate amino acids. This hypothesis has now been supported by spectroscopic studies of cobalt-substituted CysRS. Binding of cysteine, but not non-cognate amino acids, induces high absorption in the ligand-to-metal charge transfer region, providing evidence for formation of a metal-thiolate bond. In addition, mutations in the zinc ligands alter the absorption spectrum without reducing the discrimination against non-cognate amino acids. These results argue strongly for a major role for the zinc ion in amino acid discrimination by CysRS, where the tight zinc-thiolate interaction and the strict structural geometry of the metal ion are sufficient to reject serine by more than 20,000-fold at the binding step.
大肠杆菌半胱氨酰 - tRNA合成酶(CysRS)在没有编辑反应的情况下实现了高水平的氨基酸特异性。与底物半胱氨酸结合的CysRS的晶体结构表明,活性位点底部与紧密结合的锌离子直接进行硫醇配位是对非同源氨基酸选择性的主要决定因素。这一假设现在已得到钴取代的CysRS光谱研究的支持。半胱氨酸而非非同源氨基酸的结合会在配体到金属的电荷转移区域诱导高吸收,为金属硫醇盐键的形成提供了证据。此外,锌配体中的突变会改变吸收光谱,而不会降低对非同源氨基酸的区分能力。这些结果有力地证明了锌离子在CysRS进行氨基酸区分中起主要作用,其中紧密的锌 - 硫醇盐相互作用和金属离子严格的结构几何形状足以在结合步骤中将丝氨酸排斥20000倍以上。