2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Gas vesicle-blood interactions enhance ultrasound imaging contrast

      Preprint
      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Gas vesicles (GVs) are genetically encoded, air-filled protein nanostructures of broad interest for biomedical research and clinical applications, acting as imaging and therapeutic agents for ultrasound, magnetic resonance, and optical techniques. However, the biomedical applications of GVs as a systemically injectable nanomaterial have been hindered by a lack of understanding of GVs’ interactions with blood components, which can significantly impact in vivo performance. Here, we investigate the dynamics of GVs in the bloodstream using a combination of ultrasound and optical imaging, surface functionalization, flow cytometry, and mass spectrometry. We find that erythrocytes and serum proteins bind to GVs and shape their acoustic response, circulation time, and immunogenicity. We show that by modifying the GV surface, we can alter these interactions and thereby modify GVs’ in vivo performance. These results provide critical insights for the development of GVs as agents for nanomedicine.

          Related collections

          Most cited references51

          • Record: found
          • Abstract: found
          • Article: not found

          Biomolecular coronas provide the biological identity of nanosized materials.

          The search for understanding the interactions of nanosized materials with living organisms is leading to the rapid development of key applications, including improved drug delivery by targeting nanoparticles, and resolution of the potential threat of nanotechnological devices to organisms and the environment. Unless they are specifically designed to avoid it, nanoparticles in contact with biological fluids are rapidly covered by a selected group of biomolecules to form a corona that interacts with biological systems. Here we review the basic concept of the nanoparticle corona and its structure and composition, and highlight how the properties of the corona may be linked to its biological impacts. We conclude with a critical assessment of the key problems that need to be resolved in the near future.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Nanochemistry and Nanomedicine for Nanoparticle-based Diagnostics and Therapy.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Nanoparticle PEGylation for imaging and therapy.

              Nanoparticles are an essential component in the emerging field of nanomedical imaging and therapy. When deployed in vivo, these materials are typically protected from the immune system by polyethylene glycol (PEG). A wide variety of strategies to coat and characterize nanoparticles with PEG has established important trends on PEG size, shape, density, loading level, molecular weight, charge and purification. Strategies to incorporate targeting ligands are also prevalent. This article presents a background to investigators new to stealth nanoparticles, and suggests some key considerations needed prior to designing a nanoparticle PEGylation protocol and characterizing the performance features of the product.
                Bookmark

                Author and article information

                Journal
                bioRxiv
                BIORXIV
                bioRxiv
                Cold Spring Harbor Laboratory
                25 July 2023
                : 2023.07.24.550434
                Affiliations
                [1 ]Division of Chemistry and Chemical Engineering, California Institute of Technology; Pasadena, CA 91125, USA
                [2 ]Institute of Biomedical Engineering, University of Toronto; Toronto, ON M5S 3G9, Canada
                [3 ]Terence Donnelly Centre for Cellular & Biomolecular Research, University of Toronto; Toronto, ON M5S 3E1, Canada
                [4 ]Department of Chemistry, University of Toronto; Toronto, ON M5S 3H6, Canada
                [5 ]Division of Engineering and Applied Science, California Institute of Technology; Pasadena, CA 91125, USA
                [6 ]Howard Hughes Medical Institute; Pasadena, CA 91125, USA
                [7 ]These authors contributed equally to this work
                Author notes

                AUTHOR CONTRIBUTIONS

                .L, J.H.K., and M.G.S. conceptualized the research. B.L performed the in vivo imaging experiments with assistance from M.B.S. J.H.K. designed polymer synthesis and gas vesicle functionalization reactions with assistance from T.F.D. J.H.K and B.L. characterized the functionalized gas vesicles. B.L. performed the erythrocyte modeling and incubation experiments. B.S. and Y.Z. performed LC–MS/MS experiments and analyzed the data. D.M. prepared gas vesicles for experiments. All authors contributed to editing and revising the manuscript. M.G.S. and W.C.W.C. supervised the research.

                [* ]Corresponding author: mikhail@ 123456caltech.edu (MGS)
                Article
                10.1101/2023.07.24.550434
                10402017
                37546852
                98df81aa-e830-4d4e-a2a3-3caa12ab4cf2

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.

                History
                Categories
                Article

                Comments

                Comment on this article