Mayer A N, Barany F
Department of Microbiology, Hearst Microbiology Research Center, Cornell University Medical College, New York, NY 10021.
Gene. 1995 Feb 3;153(1):1-8. doi: 10.1016/0378-1119(94)00752-e.
In an effort to identify amino acid (aa) residues near the active site of TaqI restriction endonuclease (ENase), a sequence-specific photoaffinity reagent was designed. This reagent exploits the finding that modification of the Rp oxygen of the scissile phosphate does not interfere with substrate binding. The TpCGA phosphate was substituted with an Rp phosphorothioate group to direct the placement of the heterobifunctional reagent p-azidophenacyl bromide. TaqI bound the photoaffinity reagent specifically and formed a covalent adduct with the ENase in the presence of UV light. The modified aa was identified as Tyr161. This aa was changed to Phe by site-directed mutagenesis, and the resulting Y161F mutant was characterized. Removal of the Tyr161 hydroxyl group lowered both the kcat and the Km fivefold, indicating that, while this aa may be near the scissile phosphate, it is not critically required for catalysis.
为了鉴定嗜热栖热菌限制性内切酶(ENase)活性位点附近的氨基酸(aa)残基,设计了一种序列特异性光亲和试剂。该试剂利用了如下发现:可裂磷酸酯的Rp氧的修饰并不干扰底物结合。将TpCGA磷酸酯用Rp硫代磷酸酯基团取代,以指导异双功能试剂对叠氮苯甲酰溴的定位。嗜热栖热菌限制性内切酶特异性结合光亲和试剂,并在紫外光存在下与该内切酶形成共价加合物。鉴定出被修饰的氨基酸为Tyr161。通过定点诱变将该氨基酸改变为苯丙氨酸,并对所得的Y161F突变体进行了表征。去除Tyr161羟基使kcat和Km均降低了五倍,这表明,虽然该氨基酸可能靠近可裂磷酸酯,但它对于催化作用并非至关重要。