Garner Dewain K, Liang Lei, Barrios David A, Zhang Jun-Long, Lu Yi
Department of Chemistry, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, USA.
ACS Catal. 2011 Sep 2;1(9):1083-1089. doi: 10.1021/cs200258e.
Two questions important to the success in metalloenzyme design are how to attach or anchor metal cofactors inside protein scaffolds, and in what way such positioning affects enzymatic properties. We have previously reported a dual anchoring method to position a nonnative cofactor, MnSalen (1), inside the heme cavity of apo sperm whale myoglobin (Mb) and showed that the dual anchoring can increase both the activity and enantioselectivity over the single anchoring methods, making this artificial enzyme an ideal system to address the above questions. Here we report systematic investigations of the effect of different covalent attachment or anchoring positions on reactivity and selectivity of sulfoxidation by the MnSalen-containing Mb enzymes. We have found that changing the left anchor from Y103C to T39C has an almost identical effect of increasing rate by 1.8-fold and increasing selectivity by +14% for S, whether the right anchor is L72C or S108C. At the same time, regardless of the identity of the left anchor, changing the right anchor from S108C to L72C increases rate by 4-fold and selectivity by +66%. The right anchor site was observed to have a greater influence than the left anchor site on the reactivity and selectivity in sulfoxidation of a wide scope of other ortho-, meta- and para- substituted substrates. The 1•Mb(T39C/L72C) showed the highest reactivity (TON up to 2.31 min(-1)) and selectivity (ee% up to 83%) among the different anchoring positions examined. Molecular dynamic simulations indicate that these changes in reactivity and selectivity may be due to the steric effects of the linker arms inside the protein cavity. These results indicate that small differences in the anchor positions can result in significant changes in reactivity and enantioselectivity, probably through steric interactions with substrates when they enter the substrate-binding pocket, and that the effects of right and left anchor positions are independent and additive in nature. The finding that the anchoring arms can influence both the positioning of the cofactor and steric control of substrate entrance will help design better functional metalloenzymes with predicted catalytic activity and selectivity.
对于金属酶设计的成功而言,两个重要问题是如何将金属辅因子附着或固定在蛋白质支架内部,以及这种定位以何种方式影响酶的性质。我们之前报道了一种双重锚定方法,用于将非天然辅因子MnSalen(1)定位在脱辅基抹香鲸肌红蛋白(Mb)的血红素腔内,并表明双重锚定相对于单一锚定方法可以提高活性和对映选择性,使这种人工酶成为解决上述问题的理想体系。在此,我们报告了关于不同共价连接或锚定位置对含MnSalen的Mb酶催化亚砜化反应的反应性和选择性影响的系统研究。我们发现,无论右锚定是L72C还是S108C,将左锚定从Y103C变为T39C都具有几乎相同的效果,即反应速率提高1.8倍,对S的选择性提高14%。同时,无论左锚定的身份如何,将右锚定从S108C变为L72C会使反应速率提高4倍,选择性提高66%。观察到右锚定位点在广泛的其他邻位、间位和对位取代底物的亚砜化反应中,对反应性和选择性的影响比左锚定位点更大。在研究的不同锚定位置中,1•Mb(T39C/L72C)表现出最高的反应性(TON高达2.31 min⁻¹)和选择性(ee%高达83%)。分子动力学模拟表明,这些反应性和选择性的变化可能是由于蛋白质腔内连接臂的空间效应。这些结果表明,锚定位置的微小差异可能导致反应性和对映选择性的显著变化,可能是通过底物进入底物结合口袋时与底物的空间相互作用,并且左右锚定位置的影响在本质上是独立且可加的。锚定臂既能影响辅因子的定位又能影响底物进入的空间控制这一发现,将有助于设计具有预测催化活性和选择性的更好的功能性金属酶。