Li, J.; Wu, Y.; Liu, C.; Zhang, S.; Su, X.; Xie, S.; Yang, F. A Modified Tridecapeptide Probe for Imaging Cell Junction. Molecules2024, 29, 1003.
Li, J.; Wu, Y.; Liu, C.; Zhang, S.; Su, X.; Xie, S.; Yang, F. A Modified Tridecapeptide Probe for Imaging Cell Junction. Molecules 2024, 29, 1003.
Li, J.; Wu, Y.; Liu, C.; Zhang, S.; Su, X.; Xie, S.; Yang, F. A Modified Tridecapeptide Probe for Imaging Cell Junction. Molecules2024, 29, 1003.
Li, J.; Wu, Y.; Liu, C.; Zhang, S.; Su, X.; Xie, S.; Yang, F. A Modified Tridecapeptide Probe for Imaging Cell Junction. Molecules 2024, 29, 1003.
Abstract
Cell junction that is usually associated with dynamic cytoskeletons is essential for a wide range of cellular activities such as cell migration, cell communication, barrier function and signal transduction. Real-time observation of cell junction facilitates understanding of the mechanisms by which cell junction regulate relevant cellular activities. In this study, we examined the binding capacity of a modified tridecapeptide from Cx43 to cell junction protein ZO-1 and sought to create a fluorescent peptide that could be used to label cell junction. To introduce the fluorescent peptide into the cells, a cell-penetrating peptide was linked to the modified tridecapeptide and synthesized. The binding of the modified tridecapeptide was tested using pull down and immunoprecipitation assay. The ability of the peptide to label cell junction was assessed by adding it to fixed or cultured Caco-2 cells. Testing assay revealed that the Cx43-derived peptide can bind to ZO-1. Besides, the peptide was able to label cell junction of fixed cell, although no obvious cell junction labeling was observed clearly in living cells, probably due to the inadequate affinity. These results indicate that a peptide-based strategy for labeling cell junction may be feasible, and efforts to improve its affinity are warranted in the future.
Biology and Life Sciences, Cell and Developmental Biology
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