4.7 Article

Cellular uptake of a cationic amphiphilic fluorophore in the form of assemblies via Clathrin-dependent endocytosis

Journal

MATERIALS & DESIGN
Volume 200, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2021.109464

Keywords

Cellular uptake; Cationic amphiphilic fluorophores; Proteomics analysis; Clathrin-dependent endocytosis; shRNA interfering

Funding

  1. National Key R&D Program of China [2018YFE0205300, 2018YFE0205303, 2017YFA0104003]
  2. National Natural Science Foundation of China [31571517, 21674075, 31760307]
  3. Beijing Municipal Natural Science Foundation [7192091, 5202011]
  4. Natural Science Foundation of Jiangsu Province [BK20161211]
  5. Key University Science Research Project of Jiangsu Province [17KJA150007]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions

Ask authors/readers for more resources

The study investigated the cellular uptake of a cationic amphiphile TPE-11 in labeling Hela cells, revealing significant differences in fluorescent signals below and above its critical micellar concentration. Proteomics analysis identified proteins involved in the internalization process, showing that TPE-11 mainly enters cells via Clathrin-dependent endocytosis. The findings suggest that the cellular uptake mechanism demonstrated by TPE-11 may be applicable to similar cationic amphiphilic molecules.
Cellular uptake is a key step for the organic fluorophore molecules to label eukaryotic cells. Small amphiphilic fluorophores in aqueous solution present a rather complicated system, where individual molecules (monomers) or nano-scale assemblies co-exist in the solution. How and in which form do they enter into cells, and how they further gather in cells? These questions are still remain unknown to the best of our knowledge. In order to unravel the above problems, we herein studied the cellular uptake of a cationic amphiphile TPE-11, which shows strong aggregation induced emission effects in aqueous solution. Significant differences of fluorescent signals were obtained when concentration of TPE-11 applied to label Hela cells was below and above its critical micellar concentration (CMC). To elucidate the pathways for assembly forms entering into inner cells, we screened candidate proteins involving in internalization of TPE-11 in HeLa cells by using proteomics analysis, liquid chromatography plus mass spectrometry. The results indicate that TPE-11 mainly takes form of assemblies to enter into cells via Clathrin-dependent endocytosis (CDE). The result was confirmed by the specific inhibitor of the CDE pathway and knockdown of Clathrin with shRNA interfering. The cellular uptake demonstrated by TPE-11 might also apply to analogous cationic amphiphilic molecules. (C) 2021 The Author(s). Published by Elsevier Ltd.

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