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电子转移通过黄素蛋白标签驱动对比剂的光聚合用于相关显微镜。

Electron Transfer Drives the Photosensitized Polymerization of Contrast Agents by Flavoprotein Tags for Correlative Microscopy.

机构信息

Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.

Henry Eyring Center for Cell and Genome Science, University of Utah, Salt Lake City, Utah 84112, United States.

出版信息

J Am Chem Soc. 2024 Aug 28;146(34):23797-23805. doi: 10.1021/jacs.4c05397. Epub 2024 Aug 16.

Abstract

Singlet oxygen generation has long been considered the key feature that allows genetically encoded fluorescent tags to produce polymeric contrast agents for electron microscopy. Optimization of the singlet oxygen sensitization quantum yield has not included the effects of electron-rich monomers on the sensitizer's photocycle. We report that at monomer concentrations employed for staining, quenching by electron transfer is the primary deactivation pathway for photoexcitations. A simple photochemical model including contributions from both processes reproduces the observed reaction rates and indicates that most of the product is driven by pathways that involve electron transfer with monomers─not by the sensitization of singlet oxygen. Realizing the importance of these competing reaction pathways offers a new paradigm to guide the development of genetically encodable tags and suggests opportunities to expand the materials scope and growth conditions for polymeric contrast agents (e.g., biocompatible monomers, O poor environments).

摘要

单线态氧的产生一直被认为是使基因编码的荧光标记物产生用于电子显微镜的聚合物对比剂的关键特征。单线态氧敏化量子产率的优化并未包括富电子单体对敏化剂光循环的影响。我们报告说,在用于染色的单体浓度下,电子转移猝灭是光激发的主要失活途径。一个包含这两个过程的简单光化学反应模型再现了观察到的反应速率,并表明大多数产物是由涉及与单体的电子转移的途径驱动的,而不是由单线态氧的敏化驱动的。认识到这些竞争反应途径的重要性为指导基因可编码标签的发展提供了一个新的范例,并为扩大聚合物对比剂的材料范围和生长条件(例如,生物相容性单体、贫氧环境)提供了机会。

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