4.6 Article

Dissecting the Permeability of the Escherichia coli Cell Envelope to a Small Molecule Using Tailored Intensiometric Fluorescent Protein Sensors

期刊

ACS OMEGA
卷 8, 期 42, 页码 39562-39569

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.3c05405

关键词

-

向作者/读者索取更多资源

Membranes play a crucial role in defining cell boundaries and facilitating communication and nutrient uptake. However, our understanding and manipulation of the permeation of solutes across biological membranes, especially in Gram-negative bacteria, is limited. In this study, the authors use a small-molecule-responsive fluorescent protein sensor to analyze the permeability of the E. coli cell envelope. They investigate the permeation of the biotechnologically relevant macrolide rapamycin and find that recombinant expression of a nanopore in the outer membrane can enhance its permeability. This study provides insights into studying and controlling small molecule permeation in prokaryotic cells.
Membranes provide a highly selective barrier that defines the boundaries of any cell while providing an interface for communication and nutrient uptake. However, despite their central physiological role, our capacity to study or even engineer the permeation of distinct solutes across biological membranes remains rudimentary. This especially applies to Gram-negative bacteria, where the outer and inner membrane impose two permeation barriers. Addressing this analytical challenge, we exemplify how the permeability of the Escherichia coli cell envelope can be dissected using a small-molecule-responsive fluorescent protein sensor. The approach is exemplified for the biotechnologically relevant macrolide rapamycin, for which we first construct an intensiometric rapamycin detector (iRapTor) while comprehensively probing key design principles in the iRapTor scaffold. Specifically, this includes the scope of minimal copolymeric linkers as a function of topology and the concomitant need for gate post residues. In a subsequent step, we apply iRapTors to assess the permeability of the E. coli cell envelope to rapamycin. Despite its lipophilic character, rapamycin does not readily diffuse across the E. coli envelope but can be enhanced by recombinantly expressing a nanopore in the outer membrane. Our study thus provides a blueprint for studying and actuating the permeation of small molecules across the prokaryotic cell envelope.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据