The Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China.
Wuhan No. 1 Hospital, Huazhong University of Science and Technology, Wuhan, Hubei 430022, China.
J Org Chem. 2022 Jul 1;87(13):8648-8655. doi: 10.1021/acs.joc.2c00841. Epub 2022 Jun 16.
Here, we first report a rapid and highly selective biocompatible ligation that proceeds via a strain-promoted prenyl-involved [2, 3]-Ene rearrangement process. We demonstrate the usefulness of naturally occurring strain-promoted β-caryophyllene with triazoline (PTAD)/Selectfluor in the study of tagging molecule-of-interest. Experiments in peptide (Histone H3 (1-21) and Myhc (614-629)) and protein (BSA, βLG, and HSP40) models exemplified the utility of the Ene-ligation for in vivo imaging and tracking.
在这里,我们首先报道了一种快速且高度选择性的生物相容性连接反应,该反应通过应变促进的涉及[2,3]-烯重排过程进行。我们证明了天然存在的应变促进β-石竹烯与三唑啉(PTAD)/Selectfluor 在标记感兴趣分子的研究中的有用性。在肽(组蛋白 H3(1-21)和 Myhc(614-629))和蛋白质(BSA、βLG 和 HSP40)模型中的实验证明了 Ene 连接在体内成像和跟踪中的实用性。