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大肠杆菌5'-甲硫基腺苷/S-腺苷高半胱氨酸核苷酶皮摩尔和飞摩尔过渡态类似物亲和力的结构原理

Structural rationale for the affinity of pico- and femtomolar transition state analogues of Escherichia coli 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase.

作者信息

Lee Jeffrey E, Singh Vipender, Evans Gary B, Tyler Peter C, Furneaux Richard H, Cornell Kenneth A, Riscoe Michael K, Schramm Vern L, Howell P Lynne

机构信息

Structural Biology and Biochemistry, Research Institute, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.

出版信息

J Biol Chem. 2005 May 6;280(18):18274-82. doi: 10.1074/jbc.M414471200. Epub 2005 Mar 3.

Abstract

Immucillin and DADMe-Immucillin inhibitors are tight binding transition state mimics of purine nucleoside phosphorylases (PNP). 5'-Methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) is proposed to form a similar transition state structure as PNP. The companion paper describes modifications of the Immucillin and DADMe-Immucillin inhibitors to better match transition state features of MTAN and have led to 5'-thio aromatic substitutions that extend the inhibition constants to the femtomolar range (Singh, V., Evans, G. B., Lenz, D. H., Mason, J., Clinch, K., Mee, S., Painter, G. F., Tyler, P. C., Furneaux, R. H., Lee, J. E., Howell, P. L., and Schramm, V. L. (2005) J. Biol. Chem. 280, 18265-18273). 5'-Methylthio-Immucillin A (MT-ImmA) and 5'-methylthio-DADMe-Immucillin A (MT-DADMe-ImmA) exhibit slow-onset inhibition with K(i)(*) of 77 and 2 pm, respectively, and were selected for structural analysis as the parent compounds of each class of transition state analogue. The crystal structures of Escherichia coli MTAN complexed with MT-ImmA and MT-DADMe-ImmA were determined to 2.2 A resolution and compared with the existing MTAN inhibitor complexes. These MTAN-transition state complexes are among the tightest binding enzyme-ligand complexes ever described and analysis of their mode of binding provides extraordinary insight into the structural basis for their affinity. The MTAN-MT-ImmA complex reveals the presence of a new ion pair between the 4'-iminoribitol atom and the nucleophilic water (WAT3) that captures key features of the transition state. Similarly, in the MTAN-MT-DADMe-ImmA complex a favorable hydrogen bond or ion pair interaction between the cationic 1'-pyrrolidine atom and WAT3 is crucial for tight affinity. Distance analysis of the nucleophile and leaving group show that MT-ImmA is a mimic of an early transition state, while MT-DADMe-ImmA is a better mimic of the highly dissociated transition state of E. coli MTAN.

摘要

免疫菌素和二氮杂双环戊二烯免疫菌素抑制剂是嘌呤核苷磷酸化酶(PNP)紧密结合的过渡态模拟物。5'-甲硫基腺苷/S-腺苷高半胱氨酸核苷酶(MTAN)被认为能形成与PNP相似的过渡态结构。配套论文描述了对免疫菌素和二氮杂双环戊二烯免疫菌素抑制剂的修饰,使其更好地匹配MTAN的过渡态特征,并导致5'-硫代芳基取代,将抑制常数扩展到飞摩尔范围(辛格,V.,埃文斯,G. B.,伦茨,D. H.,梅森,J.,克林奇,K.,米,S.,佩因特,G. F.,泰勒,P. C.,弗诺,R. H.,李,J. E.,豪厄尔,P. L.,和施拉姆,V. L.(2005年)《生物化学杂志》280,18265 - 18273)。5'-甲硫基免疫菌素A(MT-ImmA)和5'-甲硫基二氮杂双环戊二烯免疫菌素A(MT-DADMe-ImmA)表现出缓慢起效的抑制作用,其K(i)(*)分别为77和2皮摩尔,并且作为每类过渡态类似物的母体化合物被选作结构分析。测定了与MT-ImmA和MT-DADMe-ImmA复合的大肠杆菌MTAN的晶体结构,分辨率为2.2埃,并与现有的MTAN抑制剂复合物进行了比较。这些MTAN-过渡态复合物是有史以来描述的结合最紧密的酶-配体复合物之一,对其结合模式的分析为它们亲和力的结构基础提供了非凡的见解。MTAN-MT-ImmA复合物揭示了在4'-亚氨基核糖醇原子和亲核水(WAT3)之间存在一个新的离子对,该离子对捕捉了过渡态的关键特征。同样,在MTAN-MT-DADMe-ImmA复合物中,阳离子1'-吡咯烷原子与WAT3之间有利的氢键或离子对相互作用对于紧密亲和力至关重要。亲核试剂和离去基团的距离分析表明,MT-ImmA是早期过渡态的模拟物,而MT-DADMe-ImmA是大肠杆菌MTAN高度解离过渡态的更好模拟物。

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