4.8 Article

Efficient intracellular delivery of native proteins facilitated by preorganized guanidiniums on pillar[5]arene skeleton

期刊

NANO TODAY
卷 43, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nantod.2022.101396

关键词

Pillar[5]arene; Self-assembly; Preorganization; Proteins delivery; Guanidinium

资金

  1. National Science Foundation of China [22071275, 22101310, 21871301]
  2. Science and Technology Development Fund, Macau SAR [FDCT 0065/2021/A2]
  3. Dr. Stanley Ho Medical Development Foundation [SHMDF-OIRFS/2021/002]
  4. UM Macao PhD Scholarship
  5. [SHMDF-OIRFS/2021/0 02]

向作者/读者索取更多资源

This study demonstrates the efficient delivery of proteins with different isoelectric points into various cell lines using guanidinium perfunctionalized pillar[5]arene (GP5). The densely pre-organized guanidinium groups on GP5 play a crucial role in facilitating protein binding and cellular uptake, resulting in high protein delivery potency and maintained bioactivities. This research offers valuable insights for the design of cell-penetrating peptide mimetics for protein transductions.
Due to membrane impermeability of proteins, intracellular delivery of protein is of significant challenge. Although numerous protein carriers have been reported, it remains difficult to efficiently deliver proteins with different isoelectric points into cells. Herein, guanidinium perfunctionalized pillar[5]arene (GP5) was employed for efficient delivery of proteins with different isoelectric points into different cell lines, and the bioactivities of the proteins were well maintained after intracellular delivery. After comparison with linear cell-penetrating peptides, unsymmetrical guanidinium-macrocycles, primary and quaternary ammonium functionalized pillar[5]arene derivatives, and the monomer of GP5, the high protein delivery potency of GP5 was mainly attributed to the densely pre-organized guanidinium groups on both sides of the pillar[5]arene skeleton, which could not only facilitate GP5 to bind with proteins to form protein nano-aggregates, but also promote cellular uptake of proteins via interactions with cellular surface. This study offers important new insights to the design and development of cell-penetrating peptide mimetic molecules for protein transductions.(c) 2022 Elsevier Ltd. All rights reserved.

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