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Covalent coupling of functionalized outer membrane vesicles (OMVs) to gold nanoparticles.
Bong, Ji-Hong; Dombovski, Alexander; Birus, Robin; Cho, Sua; Lee, Misu; Pyun, Jae-Chul; Jose, Joachim.
Afiliação
  • Bong JH; University of Münster, Institute of Pharmaceutical and Medicinal Chemistry, PharmaCampus, Corrensstr. 48, 48149 Münster, Germany; Department of Materials Science and Engineering, Yonsei University, 50 Yonsei-Ro, Seodaemun-Gu, 03722 Seoul, Republic of Korea; Division of Life Sciences, College of Life
  • Dombovski A; University of Münster, Institute of Pharmaceutical and Medicinal Chemistry, PharmaCampus, Corrensstr. 48, 48149 Münster, Germany.
  • Birus R; University of Münster, Institute of Pharmaceutical and Medicinal Chemistry, PharmaCampus, Corrensstr. 48, 48149 Münster, Germany.
  • Cho S; Division of Life Sciences, College of Life Science and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
  • Lee M; Division of Life Sciences, College of Life Science and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
  • Pyun JC; Department of Materials Science and Engineering, Yonsei University, 50 Yonsei-Ro, Seodaemun-Gu, 03722 Seoul, Republic of Korea. Electronic address: jcpyun@yonsei.ac.kr.
  • Jose J; University of Münster, Institute of Pharmaceutical and Medicinal Chemistry, PharmaCampus, Corrensstr. 48, 48149 Münster, Germany. Electronic address: joachim.jose@uni-muenster.de.
J Colloid Interface Sci ; 663: 227-237, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38401443
ABSTRACT
Outer membrane vesicle-functionalized nanoparticles (OMV-NPs) have attracted significant interest, especially regarding drug delivery applications and vaccines. Here, we report on novel OMV-NPs by applying bioorthogonal click reaction for encapsulating gold nanoparticles (NPs) within outer membrane vesicles (OMVs) by covalent coupling. For this purpose, outer membrane protein A (OmpA), abundant in large numbers (due to 100,000 copies/cell [1]) in OMVs, was modified via the incorporation of the unnatural amino acid p-azidophenylalanine. The azide group was covalently coupled to alkyne-functionalized NPs after incorporation into OmpA. A simplified procedure using low-speed centrifugation (1,000 x g) was developed for preparing OMV-NPs. The OMV-NPs were characterized by zeta potential, Laurdan-based lipid membrane dynamics studies, and the enzymatic activity of functionalized OMVs with surface-displayed nicotinamide adenine dinucleotide oxidase (Nox). In addition, OMVs from attenuated bacteria (ClearColiTM BL21(DE3), E. coli F470) with surface-displayed Nox or antibody fragments were prepared and successfully coupled to AuNPs. Finally, OMV-NPs displaying single-chain variable fragments from a monoclonal antibody directed against epidermal growth factor receptor were applied to demonstrate the feasibility of OMV-NPs for tumor cell targeting.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas Metálicas / Ouro Idioma: En Revista: J Colloid Interface Sci Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas Metálicas / Ouro Idioma: En Revista: J Colloid Interface Sci Ano de publicação: 2024 Tipo de documento: Article