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mRNA Delivery and Storage by Co-Assembling Nanostructures with Designer Oligopeptides.
Feng, Ruilu; Chang, Atta Cheuk Yan; Ni, Rong; Li, Jacky Cheuk Yin; Chau, Ying.
Afiliación
  • Feng R; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China.
  • Chang ACY; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China.
  • Ni R; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China.
  • Li JCY; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China.
  • Chau Y; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China.
ACS Appl Bio Mater ; 5(7): 3476-3486, 2022 07 18.
Article en En | MEDLINE | ID: mdl-35729172
ABSTRACT
Broadening the applicable tools for mRNA delivery provides more flexibility in research and those proven effective and safe can potentially be translated for clinical use. We report here a 27-amino acid peptide sequence mimicking the viral capsid protein, termed pepMAX, capable of co-assembling with mRNA into 100-150 nm nanostructures for efficient transfection of multiple cell lines. The mRNA loading and N/P ratio have been systematically optimized for each cell line. In HeLa, HEK293, and SKNMC, the transfection attained (>80%) is comparable with that of commercially available vectors Lipofectamine MessengerMAXTM (LipoMMAX). Confocal microscopy reveals that pepMAX efficiently delivers mRNA into the cytosol and induces efficient protein production. The pepMAX/mRNA co-assemblies retain their transfection efficiency after storage up to one week at room temperature in lyophilized form.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN Mensajero / Técnicas de Transferencia de Gen / Nanoestructuras Límite: Humans Idioma: En Revista: ACS Appl Bio Mater Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN Mensajero / Técnicas de Transferencia de Gen / Nanoestructuras Límite: Humans Idioma: En Revista: ACS Appl Bio Mater Año: 2022 Tipo del documento: Article País de afiliación: China