Banás Pavel, Rulísek Lubomír, Hánosová Veronika, Svozil Daniel, Walter Nils G, Sponer Jirí, Otyepka Michal
Department of Physical Chemistry and Center for Biomolecules and Complex Molecular Systems, Palacky University, tr. Svobody 26, 771 46, Olomouc, Czech Republic.
J Phys Chem B. 2008 Sep 4;112(35):11177-87. doi: 10.1021/jp802592z. Epub 2008 Aug 8.
The hepatitis delta virus (HDV) ribozyme is an RNA motif embedded in human pathogenic HDV RNA. Previous experimental studies have established that the active-site nucleotide C75 is essential for self-cleavage of the ribozyme, although its exact catalytic role in the process remains debated. Structural data from X-ray crystallography generally indicate that C75 acts as the general base that initiates catalysis by deprotonating the 2'-OH nucleophile at the cleavage site, while a hydrated magnesium ion likely protonates the 5'-oxygen leaving group. In contrast, some mechanistic studies support the role of C75 acting as general acid and thus being protonated before the reaction. We report combined quantum chemical/molecular mechanical calculations for the C75 general base pathway, utilizing the available structural data for the wild type HDV genomic ribozyme as a starting point. Several starting configurations differing in magnesium ion placement were considered and both one-dimensional and two-dimensional potential energy surface scans were used to explore plausible reaction paths. Our calculations show that C75 is readily capable of acting as the general base, in concert with the hydrated magnesium ion as the general acid. We identify a most likely position for the magnesium ion, which also suggests it acts as a Lewis acid. The calculated energy barrier of the proposed mechanism, approximately 20 kcal/mol, would lower the reaction barrier by approximately 15 kcal/mol compared with the uncatalyzed reaction and is in good agreement with experimental data.
丁型肝炎病毒(HDV)核酶是一种嵌入人类致病HDV RNA中的RNA基序。先前的实验研究已经确定,活性位点核苷酸C75对于核酶的自我切割至关重要,尽管其在该过程中的确切催化作用仍存在争议。X射线晶体学的结构数据通常表明,C75作为通用碱,通过使切割位点的2'-OH亲核试剂去质子化来启动催化作用,而水合镁离子可能使5'-氧离去基团质子化。相比之下,一些机理研究支持C75作为通用酸的作用,因此在反应前被质子化。我们以野生型HDV基因组核酶的可用结构数据为起点,报告了C75通用碱途径的量子化学/分子力学联合计算。考虑了几种镁离子位置不同的起始构型,并使用一维和二维势能面扫描来探索合理的反应路径。我们的计算表明,C75能够很容易地作为通用碱,与水合镁离子作为通用酸协同作用。我们确定了镁离子最可能的位置,这也表明它作为路易斯酸起作用。所提出机制的计算能垒约为20 kcal/mol,与无催化反应相比,将反应能垒降低约15 kcal/mol,与实验数据吻合良好。