4.7 Article

Selective membrane wrapping on differently sized nanoparticles regulated by clathrin assembly: A computational model

期刊

出版社

ELSEVIER
DOI: 10.1016/j.colsurfb.2022.112467

关键词

Nanoparticle; Endocytosis; Clathrin assembly; Size selectivity; Computer simulation

资金

  1. Fundamental Research Funds for the Central Universities, Beijing Forestry University, China [2021ZY56]
  2. Municipal Training Program of Innovation and Entrepreneurship for Undergraduates, Beijing Forestry University, China [S202010022080, S202110022040]
  3. Academic Training Program of Innovation and Entrepreneurship for Undergraduates, Beijing Forestry University, China [X202110022063]
  4. National Natural Science Foundation of China, China [31601149, 31761133009, 31871012]
  5. Program of Introducing Talents of Discipline to Universities, China, (111 project) [B13007]
  6. Special Program for Applied Research on Super Computation of the NSFC-Guangdong Joint Fund (the second phase), China

向作者/读者索取更多资源

Clathrin-mediated endocytosis has selectivity for nanoparticle size, and clathrin can modulate the process and tune the selectivity. However, the size range of clathrin assembly does not match larger nanoparticles, and clathrin can also increase the barrier of membrane wrapping on larger nanoparticles by rigidifying the local membrane patch. The competition of these factors determines whether membrane wrapping on nanoparticles is promoted or suppressed, and can be adjusted by nanoparticle-membrane adhesion strength, clathrin concentration, and inter-nanoparticle distance.
Nanoparticles (NPs) enter cells via multiple pathways, all of which are NP size dependent. Previous studies indicated that the clathrin-mediated endocytosis has different selectivity for the NP size, but the regulatory mechanism remains unclear and difficult to study at the molecular scale in vivo. By means of computer simulation, here we design membrane wrapping on differently sized NPs with mimic clathrin assembly at the opposite membrane side. With relatively large NPs readily wrapped by a pure membrane as manifested, clathrin modulates the process and tunes the size selectivity. Although finite curvature can be generated by cage-like clathrin assembly to facilitate membrane wrapping on relatively small NPs, the clathrin assemblage has a certain range of size, which is mismatched with larger NPs. Besides, the local membrane patch is rigidified by clathrin to increase the barrier of membrane wrapping on larger NPs. Competition of these items determines whether membrane wrapping on NPs is promoted or suppressed, and can be tuned by the NP-membrane adhesion strength, clathrin concentration, and inter-NP distance. Our results highlight the significance of complex environment in altering the nature of NP interaction with cell membranes, and are expected to help design NPs for biomedical applications requiring precise control of NP uptake or cell membrane attachment.

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