Huaxi MR Research Center, Department of Radiology, West China Hospital and West China School of Medicine , Sichuan University , Chengdu 610041 , China.
Department of Chemistry and Biochemistry , University of California, San Diego , La Jolla , California 92093 , United States.
Acc Chem Res. 2018 May 15;51(5):1249-1259. doi: 10.1021/acs.accounts.8b00062. Epub 2018 Apr 11.
Bioorthogonal chemistry has found increased application in living systems over the past decade. In particular, tetrazine bioorthogonal chemistry has become a powerful tool for imaging, detection, and diagnostic purposes, as reflected in the increased number of examples reported in the literature. The popularity of tetrazine ligations are likely due to rapid and tunable kinetics, the existence of high quality fluorogenic probes, and the selectivity of reaction. In this Account, we summarize our recent efforts to advance tetrazine bioorthogonal chemistry through improvements in synthetic methodology, with an emphasis on developing new routes to tetrazines and expanding the range of useful dienophiles. These efforts have removed specific barriers that previously limited tetrazine ligations and have broadened their potential applications. Among other advances, this Account describes how our group discovered new methodology for tetrazine synthesis by developing a Lewis acid-promoted, one-pot method for generating diverse symmetric and asymmetric alkyl tetrazines with functional substituents in satisfactory yields. We attached these tetrazines to microelectrodes and succeeded in controlling tetrazine ligation by changing the redox state of the reactants. Using this electrochemical control process, we were able to modify an electrode surface with redox probes and enzymes in a site-selective fashion. This Account also describes how our group improved the ability of tetrazines to act as fluorogenic probes by developing a novel elimination-Heck cascade reaction to synthesize alkenyl tetrazine derivatives. In this approach, tetrazine was conjugated to fluorophores to produce strongly quenched probes that, after bioorthogonal reaction, are "turned on" to enhance fluorescence, in many cases by >100-fold. These probes have allowed no-wash fluorescence imaging in living cells and intact animals. Finally, this Account reviews our efforts to expand the range of dienophile substrates to make tetrazine bioorthogonal chemistry compatible with specific biochemical and biomedical applications. We found that methylcyclopropene is sufficiently stable and reactive in the biological milieu to act as an efficient dienophile. The small size of the reactive tag minimizes steric hindrance, allowing cyclopropene to serve as a metabolic reporter group to reveal biological dynamics and function. We also used norbornadiene derivatives as strained dienophiles to undergo tetrazine-mediated transfer (TMT) reactions involving tetrazine ligation followed by a retro-Diels-Alder process. This TMT reaction generates a pair of nonligating products. Using nucleic acid-templated chemistry, we have combined the TMT reaction with our fluorogenic tetrazine probes to detect endogenous oncogenic microRNA at picomolar concentrations. In a further display of dienophile versatility, we used a novel vinyl ether to cage a near-infrared fluorophore in a nonfluorescent form. Then we opened the cage in a "click to release" tetrazine bioorthogonal reaction, restoring the fluorescent form of the fluorophore. Combining this label with a corresponding nucleic acid probe allowed fluorogenic detection of target mRNA. In summary, this Account describes improvements in tetrazine and dienophile synthesis and application to advance tetrazine bioorthogonal chemistry. These advances have further enabled application of tetrazine ligation chemistry, not only in fundamental research but also in diagnostic studies.
生物正交化学在过去十年中在生命系统中的应用越来越广泛。特别是,四嗪生物正交化学已成为成像、检测和诊断目的的强大工具,这反映在文献中报道的例子越来越多。四嗪连接物的流行可能是由于其快速和可调的动力学、高质量荧光探针的存在以及反应的选择性。在本报告中,我们总结了我们最近通过改进合成方法来推进四嗪生物正交化学的努力,重点是开发新的四嗪路线和扩展有用的亲二烯体的范围。这些努力消除了以前限制四嗪连接的具体障碍,并拓宽了它们的潜在应用。在其他进展中,本报告描述了我们小组如何通过开发一种路易斯酸促进的一锅法来合成具有功能取代基的各种对称和不对称烷基四嗪,以令人满意的收率来发现新的四嗪合成方法。我们将这些四嗪连接到微电极上,并通过改变反应物的氧化还原状态成功地控制了四嗪连接。使用这种电化学控制过程,我们能够以位点选择性的方式用氧化还原探针和酶修饰电极表面。本报告还描述了我们小组如何通过开发一种新的消除-Heck 级联反应来合成烯基四嗪衍生物,从而提高四嗪作为荧光探针的能力。在这种方法中,将四嗪与荧光团共轭以产生强烈猝灭的探针,在生物正交反应后,通过“打开”来增强荧光,在许多情况下增强 100 倍以上。这些探针允许在活细胞和完整动物中进行无冲洗荧光成像。最后,本报告回顾了我们扩大亲二烯体范围的努力,以使四嗪生物正交化学与特定的生化和生物医学应用兼容。我们发现甲基环丙烯在生物环境中足够稳定和反应性,可以作为有效的亲二烯体。反应标记物的小尺寸最小化了空间位阻,允许环丙烯作为代谢报告基团来揭示生物动力学和功能。我们还使用降冰片二烯衍生物作为应变亲二烯体,进行四嗪介导的转移(TMT)反应,涉及四嗪连接,随后进行反-Diels-Alder 过程。该 TMT 反应生成一对不连接的产物。使用核酸模板化学,我们将 TMT 反应与我们的荧光四嗪探针结合,以皮摩尔浓度检测内源性致癌 microRNA。亲二烯体多功能性的进一步展示是,我们使用一种新型乙烯基醚将近红外荧光团笼封在非荧光形式中。然后,我们在“点击释放”四嗪生物正交反应中打开笼子,恢复荧光团的荧光形式。将这种标记物与相应的核酸探针结合,允许对靶 mRNA 进行荧光检测。总之,本报告描述了四嗪和亲二烯体合成的改进及其在推进四嗪生物正交化学中的应用。这些进展进一步实现了四嗪连接化学的应用,不仅在基础研究中,而且在诊断研究中也是如此。