Cell-free production of target-directed liposomes utilizing membrane localization peptides

Cell-free protein synthesis technology is a powerful tool for the rapid production of bioactive molecules such as antibodies. By combining with liposomes, immobilizing the synthesized proteins onto the liposome membrane leads production of bioactive liposomes within the cell-free reaction. These cell-free approaches can be applied in medical treatment and drug development, however, not many studies have been done to develop it as a highly versatile platform. Here, we explored hydrophobic amino acid sequences that lead hydrophilic proteins onto the liposome membrane and applied them to the co-translational production of bioactive liposomes. The membrane localizing peptides (MLPs) introduced at the N- or C-terminus of small molecular weight antibodies, nanobody, guided the membrane localization onto liposomes. The nanobodies-decorated liposomes specifically bound to cancer cells expressing the target antigen protein, thus suggesting maintaining functional structure on the liposome membrane. The MLPs we discovered can be widely applied to the rapid immobilization of proteins on liposome surfaces, leading to cell-free applications in virus-like particles or RNA therapy.

Authors

Institutions

Publication Details

Journal
Journal of Controlled Release
Published
2025-10-18
DOI
https://doi.org/10.1016/j.jconrel.2025.114343
Citations
2
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
1.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cell-free production of target-directed liposomes utilizing membrane localization peptides

Yutetsu Kuruma, Yasuhiro Shimane, Yuji Sakai, K. Kuno
2 citations
Journal of Controlled Release
RNA Interference and Gene Delivery
1.61
article

Cell-free production of target-directed liposomes utilizing membrane localization peptides

Yutetsu Kuruma, Yasuhiro Shimane, Yuji Sakai, K. Kuno
article en
2 citations

Abstract

Cell-free protein synthesis technology is a powerful tool for the rapid production of bioactive molecules such as antibodies. By combining with liposomes, immobilizing the synthesized proteins onto the liposome membrane leads production of bioactive liposomes within the cell-free reaction. These cell-free approaches can be applied in medical treatment and drug development, however, not many studies have been done to develop it as a highly versatile platform. Here, we explored hydrophobic amino acid sequences that lead hydrophilic proteins onto the liposome membrane and applied them to the co-translational production of bioactive liposomes. The membrane localizing peptides (MLPs) introduced at the N- or C-terminus of small molecular weight antibodies, nanobody, guided the membrane localization onto liposomes. The nanobodies-decorated liposomes specifically bound to cancer cells expressing the target antigen protein, thus suggesting maintaining functional structure on the liposome membrane. The MLPs we discovered can be widely applied to the rapid immobilization of proteins on liposome surfaces, leading to cell-free applications in virus-like particles or RNA therapy.

Journal of Controlled ReleaseVol. 388(Pt 1)
Japan Agency for Marine-Earth Science and Technology (JP), Yokohama City University (JP)
Openalex Percentile: Top 14%
RNA Interference and Gene Delivery
1.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.