Tagaya M, Yagami T, Fukui T
J Biol Chem. 1987 Jun 15;262(17):8257-61.
Adenosine diphosphopyridoxal, the affinity labeling reagent specific for a lysyl residue in the nucleotide-binding site of several enzymes (Tagaya, M., and Fukui, T. (1986) Biochemistry 25, 2958-2964; Tamura, J. K., Rakov, R. D., and Cross R. L. (1986) J. Biol. Chem. 261, 4126-4133) was applied to adenylate kinase from rabbit muscle. Incubation of the enzyme with a low concentration of the reagent at 25 degrees C for 20 min followed by reduction by sodium borohydride resulted in rapid inactivation of the enzyme. Extrapolation to 100% loss of enzyme activity gave a value of 1.0 mol of the reagent per mol of enzyme. ADP, ATP, and MgATP almost completely protected the enzyme from inactivation, whereas AMP offered little retardation of the inactivation. Dilution of the inactivated enzyme which had not been treated with the reducing reagent led to restoration of enzyme activity. This reactivation was accelerated by ATP but not by AMP. Structural study of the labeled peptide showed that Lys21 is exclusively labeled by adenosine diphosphopyridoxal. These results suggest that the epsilon-amino group of Lys21 is located in the ATP-binding site of the enzyme, more specifically at or close to the subsite for the gamma-phosphate of the nucleotide.
二磷酸吡哆醛,一种对几种酶的核苷酸结合位点中的赖氨酰残基具有特异性的亲和标记试剂(田谷,M.,和福井,T.(1986年)《生物化学》25卷,2958 - 2964页;田村,J.K.,拉科夫,R.D.,和克罗斯,R.L.(1986年)《生物化学杂志》261卷,4126 - 4133页)被应用于兔肌肉中的腺苷酸激酶。将该酶与低浓度的试剂在25℃下孵育20分钟,然后用硼氢化钠还原,导致酶迅速失活。外推至酶活性完全丧失时,得到每摩尔酶消耗1.0摩尔试剂的值。ADP、ATP和MgATP几乎完全保护酶不被失活,而AMP对失活的抑制作用很小。未用还原试剂处理的失活酶稀释后导致酶活性恢复。这种再活化被ATP加速,但不被AMP加速。对标记肽的结构研究表明,赖氨酸21仅被二磷酸吡哆醛标记。这些结果表明,赖氨酸21的ε-氨基位于该酶的ATP结合位点,更具体地说,位于核苷酸γ-磷酸的亚位点或其附近。