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一种用于细胞连接成像的改良十三肽探针。

A Modified Tridecapeptide Probe for Imaging Cell Junction.

作者信息

Li Jingrui, Wu Yuhan, Liu Chunyu, Zhang Shu, Su Xin, Xie Songbo, Yang Fengtang

机构信息

School of Life Sciences and Medicine, Shandong University of Technology, Zibo 255000, China.

Center for Cell Structure and Function, Shandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong, College of Life Sciences, Shandong Normal University, Jinan 250014, China.

出版信息

Molecules. 2024 Feb 25;29(5):1003. doi: 10.3390/molecules29051003.

Abstract

Cell junctions, which are typically associated with dynamic cytoskeletons, are essential for a wide range of cellular activities, including cell migration, cell communication, barrier function and signal transduction. Observing cell junctions in real-time can help us understand the mechanisms by which they regulate these cellular activities. This study examined the binding capacity of a modified tridecapeptide from Connexin 43 (Cx43) to the cell junction protein zonula occludens-1 (ZO-1). The goal was to create a fluorescent peptide that can label cell junctions. A cell-penetrating peptide was linked to the modified tridecapeptide. The heterotrimeric peptide molecule was then synthesized. The binding of the modified tridecapeptide was tested using pulldown and immunoprecipitation assays. The ability of the peptide to label cell junctions was assessed by adding it to fixed or live Caco-2 cells. The testing assays revealed that the Cx43-derived peptide can bind to ZO-1. Additionally, the peptide was able to label cell junctions of fixed cells, although no obvious cell junction labeling was observed clearly in live cells, probably due to the inadequate affinity. These findings suggest that labeling cell junctions using a peptide-based strategy is feasible. Further efforts to improve its affinity are warranted in the future.

摘要

细胞连接通常与动态细胞骨架相关联,对于广泛的细胞活动至关重要,包括细胞迁移、细胞通讯、屏障功能和信号转导。实时观察细胞连接有助于我们理解它们调节这些细胞活动的机制。本研究检测了来自连接蛋白43(Cx43)的一种修饰十三肽与细胞连接蛋白紧密连接蛋白1(ZO-1)的结合能力。目标是创建一种能够标记细胞连接的荧光肽。将一种细胞穿透肽与修饰的十三肽相连。然后合成异源三聚体肽分子。使用下拉和免疫沉淀试验检测修饰十三肽的结合情况。通过将该肽添加到固定或活的Caco-2细胞中来评估其标记细胞连接的能力。测试分析表明,源自Cx43的肽可以与ZO-1结合。此外,该肽能够标记固定细胞的细胞连接,尽管在活细胞中未明显观察到明显的细胞连接标记,这可能是由于亲和力不足。这些发现表明使用基于肽的策略标记细胞连接是可行的。未来有必要进一步努力提高其亲和力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4023/10935238/06a357bb9b87/molecules-29-01003-g001.jpg

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