TY - JOUR
T1 - Induction of Spontaneous Liposome Adsorption by Exogenous Surface Modification with Cell-Penetrating Peptide-Conjugated Lipids
AU - Sato, Yuya
AU - Asawa, Kenta
AU - Huang, Tianwei
AU - Noiri, Makoto
AU - Nakamura, Naoko
AU - Ekdahl, Kristina N.
AU - Nilsson, Bo
AU - Ishihara, Kazuhiko
AU - Teramura, Yuji
N1 - Funding Information:
This research was supported in part by a Bilateral Joint Research Project (Japan-Sweden) of the Japan Society for the Promotion of Science (JSPS) and STINT; a Grant-in-Aid for Scientific Research (B) (26702017), a Grant-in-Aid for Scientific Research for Fostering Joint International Research (15KK0230, 18KK0305), and a Grant-in-Aid for Challenging Research (Exploratory) (19K22951) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan; StemTherapy; and grants 2018-04199, 2016-2075-5.1, and 2016-04519 from the Swedish Research Council. The research project RELIEF has received funding from the Eurostars-2 joint program (project ID: E! 113670) with cofunding from the European Union Horizon 2020 research and innovation program and further cofunding for the French, German, Dutch, Swedish partners from BPIfrance, the German Federal Ministry of Education and Research, RVO, VINNOVA.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/8/17
Y1 - 2021/8/17
N2 - The use of amphiphilic molecules such as poly(ethylene glycol)-conjugated phospholipid (PEG-lipid) enables incorporation into liposome surfaces by exogenous addition as a result of the self-assembly with lipids. This technique can be applicable for manipulation of both liposomes and cells. In this study, we aimed to characterize Tat peptide (YGRKKRRQRRR)-conjugated PEG-lipids when used to exogenously surface modify liposomes (size: ca. 100 nm). We earlier reported that cells, which were surface modified with Tat peptides conjugated to PEG-lipids could attach spontaneously to material surfaces without any chemical modification. Here, we synthesized different types of Tat-PEG-lipids by combining PEG of different molecular weights (5 and 40 kDa) with different lipids with three acyl chains (myristoyl, palmitoyl, and stearoyl, respectively) and then studied the spontaneous adsorption of modified liposomes onto a substrate surface induced by the different Tat-PEG-lipids. The amount of adsorbed liposomes strongly depended on the number of incorporated Tat-PEG-lipid moieties: a decrease in both the PEG and the acyl chain lengths led to adsorption of higher amounts of liposomes. Furthermore, when a collagenase-cleavable amino acid sequence was inserted between the Tat sequence and the PEG segment, adsorbed liposomes could be harvested from the substrate by collagenase treatment with no difference in desorption efficiency between the different Tat-PEG-lipids. Thus, Tat-PEG-lipid can be a suitable tool for the manipulation of liposomes and cells.
AB - The use of amphiphilic molecules such as poly(ethylene glycol)-conjugated phospholipid (PEG-lipid) enables incorporation into liposome surfaces by exogenous addition as a result of the self-assembly with lipids. This technique can be applicable for manipulation of both liposomes and cells. In this study, we aimed to characterize Tat peptide (YGRKKRRQRRR)-conjugated PEG-lipids when used to exogenously surface modify liposomes (size: ca. 100 nm). We earlier reported that cells, which were surface modified with Tat peptides conjugated to PEG-lipids could attach spontaneously to material surfaces without any chemical modification. Here, we synthesized different types of Tat-PEG-lipids by combining PEG of different molecular weights (5 and 40 kDa) with different lipids with three acyl chains (myristoyl, palmitoyl, and stearoyl, respectively) and then studied the spontaneous adsorption of modified liposomes onto a substrate surface induced by the different Tat-PEG-lipids. The amount of adsorbed liposomes strongly depended on the number of incorporated Tat-PEG-lipid moieties: a decrease in both the PEG and the acyl chain lengths led to adsorption of higher amounts of liposomes. Furthermore, when a collagenase-cleavable amino acid sequence was inserted between the Tat sequence and the PEG segment, adsorbed liposomes could be harvested from the substrate by collagenase treatment with no difference in desorption efficiency between the different Tat-PEG-lipids. Thus, Tat-PEG-lipid can be a suitable tool for the manipulation of liposomes and cells.
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U2 - 10.1021/acs.langmuir.1c01072
DO - 10.1021/acs.langmuir.1c01072
M3 - Article
C2 - 34342462
AN - SCOPUS:85113372146
SN - 0743-7463
VL - 37
SP - 9711
EP - 9723
JO - Langmuir
JF - Langmuir
IS - 32
ER -