Viral Mimetic Bacterial Outer Membrane Vesicles for Targeting Angiotensin-Converting Enzyme 2

  • Ahn, Gna
  • Yoon, Hyo-Won
  • Jeong, Ju Hwan
  • Kim, Yang-Hoon
  • Shin, Woo-Ri
  • 외 2명
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초록

Purpose: Outer membrane vesicles (OMVs) derived from Gram-negative bacteria naturally serve as a heterologous nano-engineering platform, functioning as effective multi-use nanovesicles for diagnostics, vaccines, and treatments against pathogens. To apply refined OMVs for human theranostic applications, we developed naturally exposed receptor-binding domain (RBD) OMVs grafted with antigen 43 as a minimal modular system targeting angiotensin-converting enzyme 2 (ACE2). Methods: We constructed E. coli-derived OMVs using the antigen 43 autotransporter system to display RBD referred to as viral mimetic Ag433700_RBD OMVs. Based on this, Ag433700_RBD protein were expressed onto Escherichia coli (E. coli) membrane. Artificial viral mimetic Ag433700_RBD OMVs were fabricated by self-assembly through membrane disruption of the Ag433700_RBD E. coli using a chemical detergent mainly containing lysozyme. Through serial centrifugation to purify fabricated OMVs, spherical Ag433700_RBD OMVs with an average diameter of 218 nm were obtained. The confirmation of the RBD expressed on OMVs was performed using trypsin treatment. Results: Our viral mimetic Ag433700_RBD OMVs had an impact on the theranostic studies: (i) angiotensin-converting enzyme 2 blockade assay, (ii) enzyme-linked immunosorbent assay for the OMVs, and (iii) intracellular uptake and neutralization assay. As serodiagnostic surrogates, Ag433700_RBD OMVs were applied to ACE2 blockade and OMVs-ELISA assay to quantify neutralization antibodies (nAbs). They reduced the robust immune response in vitro, especially IL-6 and IL-13. Experiments in mice, Ag433700_RBD OMVs was successfully proven to be safe and effective; they produced a detectable level of nAbs with 39-58% neutralisation and reduced viral titres in the lungs and brain without weight loss. Conclusion: The developed viral mimetic Ag433700_RBD OMVs may therefore be applied as a nanovesicle-theranostic platform for further emerging infectious disease-related diagnosis, vaccination, and treatment.

키워드

outer membrane vesicleantigen 43 autotransporterstargeted delivery vehicletheranosticsangiotensin-converting enzyme 2ESCHERICHIA-COLI
제목
Viral Mimetic Bacterial Outer Membrane Vesicles for Targeting Angiotensin-Converting Enzyme 2
저자
Ahn, GnaYoon, Hyo-WonJeong, Ju HwanKim, Yang-HoonShin, Woo-RiSong, Min-SukAhn, Ji-Young
DOI
10.2147/IJN.S497742
발행일
2025-01
유형
Article
저널명
International journal of nanomedicine
20
페이지
669 ~ 684