Design and Evolution of Photo-Enzymes for Stereoselective Transformations of Nitrogen Radicals

酶是非常强大的催化剂，可以识别分子底物并在活性部位处理它们。它们通常只由20个氨基酸组成，它们的催化机制通常由氨基酸侧链中的化学基团组装而成。但在这些侧链中，只有不到一半的侧链含有能够参与酶催化循环的官能团，这严重限制了酶活性部位内可想象的机制的范围。这提出了一个耐人寻味的问题，即是否可以通过使用扩展的氨基酸字母表来扩大酶的催化能力，从而为催化提供更广泛的侧链。近年来，我们团队开始朝着实现这一雄心勃勃的愿景迈出重大步伐(例如，《自然》2019、570、219、J.Am化学。SoC。2018年、140年、1535年，J.Am化学。SoC。2016年，138,11344)。我们的方法利用工程细胞翻译组件来选择性地安装包含功能侧链的非规范氨基酸。与化学修饰蛋白质结构的替代方法相比，基因编码非正则功能提供了巨大的优势：它极大地促进了定义明确、均一的蛋白质的生产；它允许在任何位置、任何蛋白质支架中引入非正则氨基酸；也许最重要的是，它允许使用定向进化来快速优化酶的性质。受小分子有机催化的机械策略的启发，我们最近结合遗传密码扩展、计算酶设计和实验室进化来创造利用非规范氨基酸作为催化亲核试剂的酶(自然2019,570,219)。这项研究现在为酶设计师和工程师打开了新的和令人兴奋的机会，这将在这个博士生中得到充分的探索。不受遗传密码的限制，学生将使用我们先进的酶工程技术来创造具有自然界中没有观察到的功能的酶，这些功能以前被认为是生物催化领域无法获得的。该项目将专门致力于创造促进对映体选择性光氧化还原转化的酶。近年来，Leonori小组(项目合作伙伴)开发了大量有价值的光氧化还原过程，涉及中间代氮自由基。目前，这些转化反应产生外消旋产物，开发这些反应的对映选择性版本仍然是一个关键的未解决的挑战。为了达到这一目标，我们将利用我们实验室提供的工程化细胞翻译组件来嵌入具有合适性质的有机辅助因子，以将光诱导电子转移中介到设计的活性部位。在这里，我们可以利用蛋白质支架提供的分子识别元件来实现对映体选择性转化。值得注意的是，有希望的初始设计可以通过迭代几轮定向进化来大幅改进，以提供用于生产高价值分子的高效和选择性的光氧化还原酶。

Enzymes are exceptionally powerful catalysts that recognize molecular substrates and process them in active sites. They are generally built from just 20 amino acids, and their catalytic machinery is typically assembled from chemical groups in the amino-acid side chains. But fewer than half of these side chains contain functional groups that can participate in enzyme catalytic cycles, which severely restricts the range of mechanisms conceivable within enzyme active sites. This raises the intriguing question of whether the catalytic repertoire of enzymes could be expanded by using an extended 'alphabet' of amino acids that offers a wider range of side chains for catalysis. In recent years our group have begun to take major strides towards achieving this ambitious vision (e.g. Nature 2019, 570, 219, J. Am. Chem. Soc. 2018, 140, 1535, J. Am. Chem. Soc. 2016, 138, 11344).Our approach exploits engineered cellular translation components to selectively install non-canonical amino acids containing functional side chains. Genetically encoding the non-canonical functionality offers enormous advantages over alternative methods for chemically modifying protein structure: it greatly facilitates the production of well-defined, homogeneous proteins; it allows the non-canonical amino acid to be introduced at any site, in any protein scaffold; and, perhaps most significantly, it allows for rapid optimization of enzyme properties using directed evolution. Inspired by mechanistic strategies from small molecule organocatalysis, we have recently employed a combination of genetic code expansion, computational enzyme design and laboratory evolution to create enzymes that exploit non-canonical amino acids as catalytic nucleophiles (Nature 2019, 570, 219). This study now opens up new and exciting opportunities to enzyme designers and engineers which will be fully explored within this PhD studentship. Free from the constraints of the genetic code, the student will employ our advanced enzyme engineering techniques to create enzymes with functions not observed in Nature, that were previously thought inaccessible to the field of biocatalysis.The project will specifically aim to create enzymes that promote enantioselective photo-redox transformations. In recent years, the Leonori group (project partner) have developed a wealth of valuable photo-redox processes involving the intermediate generation of nitrogen radicals. At present, these transformations produce racemic products, and the development of enantioselective versions of these reactions remains a key unresolved challenge. To address the objective, we will exploit engineered cellular translation components available in our laboratory to embed organic cofactors with suitable properties for mediating photo-induced electron transfers into designed active sites. Here we can take advantage of molecular recognition elements provided by the protein scaffold to achieve enantioselective conversions. Significantly, promising starting designs can be substantially improved through iterative rounds of directed evolution to afford highly efficient and selective photo-redox enzymes for the production of high value molecules.