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基于生理条件下基于香叶烯的烯丙基化反应和三氮唑/Selectfluor 实现的生物相容性连接的发展。

Development of Biocompatible Ene-Ligation Enabled by Prenyl-Based β-Caryophyllene with Triazoline/Selectfluor under Physiological Conditions.

机构信息

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.

出版信息

J Org Chem. 2022 Jul 1;87(13):8648-8655. doi: 10.1021/acs.joc.2c00841. Epub 2022 Jun 16.

Abstract

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.

摘要

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。

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