使用进化光酶的区域选择性基质化
Claire G Page1,2, Jingzhe Cao1,2, Daniel G Oblinsky2
1Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14850, United States.
Journal of the American Chemical Society
|May 18, 2023
概括
研究人员开发了一种生物催化剂控制的区域选择性化方法,克服了传统催化剂的局限性. 这种酶工程方法精确地针对异质的特定位置,提供了新的合成可能性.
科学领域:
- 有机化学
- 生物催化
- 酶工程
背景情况:
- 替代基因在药物化学中至关重要,需要有效的合成途径.
- 目前的区域选择性C-H功能化方法对体具有适度的选择性,主要受到基板电子的影响.
研究的目的:
- 开发一种由生物催化剂控制的区域选择性化丰富电子和缺电子的异质.
- 在具有挑战性的位置进行选择性化,例如C4的化酶 (ERED).
主要方法:
- 一个非选择性的ERED (GluER-T36A) 的定向演化,以实现区域选择性化.
- 涉及电荷转移 (CT) 复杂分析的机制研究,以了解选择性决定因素.
- 与其他ERED变体进行蛋白质工程和比较机制研究.
主要成果:
- 一种进化的ERED变种选择性地化了先前难以进入的C4位置.
- 机械研究显示,活动部位的修改改变了CT复合体的电子特性,增强了地面状态的CT.
- 进化轨迹表明抑制竞争途径,导致选择性得到改善.
结论:
- 酶可以在激素反应中实现高区域选择性,超过小分子催化剂的能力.
- 这种生物催化方法为合成复杂的替代提供了一个强大的策略,可以精确控制化位点.
更多相关视频
相关概念视频
Radical Reactivity: Nucleophilic Radicals
2.1K
Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For...
2.1K
Radical Anti-Markovnikov Addition to Alkenes: Overview
3.4K
The addition of hydrogen bromide to alkenes in the presence of hydroperoxides or peroxides proceeds via an anti-Markovnikov pathway and yields alkyl bromides.
3.4K
Regioselectivity of Electrophilic Additions-Peroxide Effect
8.7K
In the presence of organic peroxides, the addition of hydrogen bromide to an alkene yields the isomer that is not predicted by Markovnikov’s rule. For example, the addition of hydrogen bromide to 2-methylpropene in the presence of peroxides gives 1-bromo-2-methylpropane. This addition reaction proceeds via a free radical mechanism, which reverses the regioselectivity. The free radical reaction mechanism involves three stages: initiation, propagation, and termination.
8.7K
Radical Reactivity: Overview
2.1K
Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired...
2.1K
Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule
14.4K
If a set of reactants can yield multiple constitutional isomers, but one of the isomers is obtained as the major product, the reaction is said to be regioselective. In such reactions, bond formation or breaking is favored at one reaction site over others.
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
14.4K
Photochemical Electrocyclic Reactions: Stereochemistry
1.9K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.9K
![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)

