Nanoscale Visualization of Morphological Alteration of Live-Cell Membranes by the Interaction with Oligoarginine Cell-Penetrating Peptides

被引:11
|
作者
Ida, Hiroki [1 ,3 ,4 ,8 ]
Takahashi, Yasufumi [1 ,2 ]
Kumatani, Akichika [3 ,4 ,5 ,6 ]
Shiku, Hitoshi [4 ]
Murayama, Tomo [7 ]
Hirose, Hisaaki [7 ]
Futaki, Shiroh [7 ]
Matsue, Tomokazu [4 ]
机构
[1] Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol, Kawaguchi, Saitama 3320012, Japan
[2] Kanazawa Univ, WPI Nano Life Sci Inst WPI NanoLSI, Kanazawa, Ishikawa 9201192, Japan
[3] Tohoku Univ, Adv Inst Mat Res, Sendai, Miyagi 9808577, Japan
[4] Tohoku Univ, Grad Sch Environm Studies, Sendai, Miyagi 9808579, Japan
[5] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton, Tsukuba, Ibaraki 3050044, Japan
[6] Tohoku Univ, Ctr Sci & Innovat Spintron CSIS, Sendai, Miyagi 9808577, Japan
[7] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
[8] Tohoku Univ, Frontier Res Inst Interdisciplinary Sci, Sendai, Miyagi 9808578, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
This work was supported by World Premier International Research Center Initiative (WPI) from MEXT; Japan; PRESTO; (JPMJPR14FA; JPMJPR18H1) and CREST (grant no JPMJCR18H5) from the Japan Science and Technology Agency ([!text type='JS']JS[!/text]T); a grant-in-aid for Scientific Research (A) (19H00993) from the Japan Society for the Promotion of Science ([!text type='JS']JS[!/text]PS). S.F. was also supported by [!text type='JS']JS[!/text]PS KAKENHI (grant nos 18H04403 and 18H04017). A.K. was supported by [!text type='JS']JS[!/text]PS KAKENHI (grant nos 17K19135). H.I. was partially supported by a grant-in-aid for Research Activity Start-up (19K23643) from [!text type='JS']JS[!/text]PS KAKENHI. Y.T. was also supported by [!text type='JS']JS[!/text]PS KAKENHI (20H02582); Kurita Water and Environment Foundation; Mitani foundation for research and development; the foundation for the Promotion of ion engineering; Nakatani foundation; Novartis research foundation; CASIO science promotion foundation. H.I. and T.M. are grateful for the [!text type='JS']JS[!/text]PS Research Fellowship for Young Scientists. H.I. is also grateful for the support of a grant-in-aid of Tohoku University Institute for Promoting Graduate Degree Programs Division for Interdisciplinary Advanced Research and Education. H.I. and A.K. acknowledge to the advanced target project funds of the WPI-AIMR;
D O I
10.1021/acs.analchem.0c04097
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The interactions between the cell membrane and biomolecules remain poorly understood. For example, arginine-rich cell-penetrating peptides (CPPs), including octaarginines (R8), are internalized by interactions with cell membranes. However, during the internalization process, the exact membrane dynamics introduced by these CPPs are still unknown. Here, we visualize arginine-rich CPPs and cell-membrane interaction-induced morphological changes using a system that combines scanning ion-conductance microscopy and spinning-disk confocal microscopy, using fluorescently labeled R8. This system allows time-dependent, nanoscale visualization of structural dynamics in live-cell membranes. Various types of membrane remodeling caused by arginine-rich CPPs are thus observed. The induction of membrane ruffling and the cup closure are observed as a process of endocytic uptake of the peptide. Alternatively suggested is the concave structural formation accompanied by direct peptide translocation through cell membranes. Studies using R8 without fluorescent labeling also demonstrate a non-negligible effect of the fluorescent moiety on membrane structural alteration.
引用
收藏
页码:5383 / 5393
页数:11
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