TY - JOUR
T1 - Nanoscale Visualization of Morphological Alteration of Live-Cell Membranes by the Interaction with Oligoarginine Cell-Penetrating Peptides
AU - Ida, Hiroki
AU - Takahashi, Yasufumi
AU - Kumatani, Akichika
AU - Shiku, Hitoshi
AU - Murayama, Tomo
AU - Hirose, Hisaaki
AU - Futaki, Shiroh
AU - Matsue, Tomokazu
N1 - Funding Information:
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 (JST); a grant-in-aid for Scientific Research (A) (19H00993) from the Japan Society for the Promotion of Science (JSPS). S.F. was also supported by JSPS KAKENHI (grant nos 18H04403 and 18H04017). A.K. was supported by JSPS KAKENHI (grant nos 17K19135). H.I. was partially supported by a grant-in-aid for Research Activity Start-up (19K23643) from JSPS KAKENHI. Y.T. was also supported by JSPS 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 JSPS 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.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/4/6
Y1 - 2021/4/6
N2 - 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.
AB - 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.
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U2 - 10.1021/acs.analchem.0c04097
DO - 10.1021/acs.analchem.0c04097
M3 - Article
AN - SCOPUS:85104913584
SN - 0003-2700
VL - 93
SP - 5383
EP - 5393
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 13
ER -