Abstract:Virus-based nanoparticles (VNPs) can serve as containers for inorganic nanomaterials with excellent physical and chemical properties. Incorporation of nanomaterials inside the inner cavity of VNPs has opened up lots of possibilities for imaging applications in the field of biology and medicine. Encapsulation of inorganic nanoparticles (NPs) in VNPs can achieve the labeling of VNPs with nanoprobes and maintain the original outer surface features of VNPs at the same time. In return, VNPs enhance the stability an… Show more
“…The development of biosensors still faces the problems of low sensitivity, specificity, and interference from complex biological components . Viruses are increasingly used to construct biosensors, as they can be easily conjugated or biologically engineered . In particular, the bacteriophages that can display a wide range of foreign ligands have been involved in the development of biosensors using different methods such as the colorimetric, electrochemical, immune, fluorescence, or Raman techniques .…”
In nature, the biomineralization processes of living organisms produce a wide range of organic-inorganic hybrid materials to achieve various functions. In particular, egg shells can provide extra protection for embryos and maintain air exchange. Inspired by such phenomena, it is assumed that the engineering of organisms with biomimetic materials can lead to significant improvement in organism function. This review summarizes recent progress in biomineralization-based techniques for organism engineering, and demonstrates the therapeutic potential enabled by these techniques. The design and synthesis approaches of biomineralization-based engineering are systemically introduced to guide the controlled modification of different organisms including viruses, bacteria, cells, and proteins using in situ biomineralization, bottom-up self-assembly, chemical and genetic engineering. Tailored organisms promise delivery, protection, cell therapy, vaccine improvement as well as therapeutic detection and imaging. The present review aims to propose a biomineralization-based strategy to promote functional evolution of these organisms, which promises to meet the increasing demand for new therapeutic purpose.
“…The development of biosensors still faces the problems of low sensitivity, specificity, and interference from complex biological components . Viruses are increasingly used to construct biosensors, as they can be easily conjugated or biologically engineered . In particular, the bacteriophages that can display a wide range of foreign ligands have been involved in the development of biosensors using different methods such as the colorimetric, electrochemical, immune, fluorescence, or Raman techniques .…”
In nature, the biomineralization processes of living organisms produce a wide range of organic-inorganic hybrid materials to achieve various functions. In particular, egg shells can provide extra protection for embryos and maintain air exchange. Inspired by such phenomena, it is assumed that the engineering of organisms with biomimetic materials can lead to significant improvement in organism function. This review summarizes recent progress in biomineralization-based techniques for organism engineering, and demonstrates the therapeutic potential enabled by these techniques. The design and synthesis approaches of biomineralization-based engineering are systemically introduced to guide the controlled modification of different organisms including viruses, bacteria, cells, and proteins using in situ biomineralization, bottom-up self-assembly, chemical and genetic engineering. Tailored organisms promise delivery, protection, cell therapy, vaccine improvement as well as therapeutic detection and imaging. The present review aims to propose a biomineralization-based strategy to promote functional evolution of these organisms, which promises to meet the increasing demand for new therapeutic purpose.
“…Additionally, altering the interior surface of CCMV from cationic to anionic to promote oxidative hydrolysis can lead to size-constrained iron oxide formation within the capsid (Douglas et al, 2002). Since these early reports, other viruses have also been used as containers for biomineralization of inorganic metal-based nanoparticles, as reviewed elsewhere (Bain & Staniland, 2015;W. Zhang et al, 2017).…”
The fields of physical, chemical, and synthetic virology work in partnership to reprogram viruses as controllable nanodevices. Physical virology provides the fundamental biophysical understanding of how virus capsids assemble, disassemble, display metastability, and assume various configurations. Chemical virology considers the virus capsid as a chemically addressable structure, providing chemical pathways to modify the capsid exterior, interior, and subunit interfaces. Synthetic virology takes an engineering approach, modifying the virus capsid through rational, combinatorial, and bioinformatics-driven design strategies. Advances in these three subfields of virology aim to develop virus-based materials and tools that can be applied to solve critical problems in biomedicine and biotechnology, including applications in gene therapy and drug delivery, diagnostics, and immunotherapy. Examples discussed include mammalian viruses, such as adeno-associated virus (AAV), plant viruses, such as cowpea mosaic virus (CPMV), and bacterial viruses, such as Qβ bacteriophage. Importantly, research efforts in physical, chemical, and synthetic virology have further unraveled the design principles foundational to the form and function of viruses.
“…From a material point of view, they have certain appealing features, including nanoscale size (20–200 nm), structural symmetry, good biocompatibility, three interfaces for functionalization, facile chemical and genetic modification, and green biosynthesis in engineered organisms. [ 1–3 ] Because of these valuable characteristics, VLPs have been used as nanoplatforms for the templated synthesis of nanomaterials, [ 4–6 ] the hierarchical assembly of nanostructures, [ 7–10 ] bioimaging, [ 11 ] nanoreactors, [ 12–14 ] drug carriers, [ 15 ] and vaccines. [ 16–19 ]…”
Self-assembled virus-like particles (VLPs) hold great potential as natural nanomaterials for applications in many fields. For such purposes, monodisperse size distribution is a desirable property. However, the VLPs of simian virus 40 (SV40), a representative VLP platform, are characterized by polymorphism. In an attempt to eliminate the polymorphism, 15 mutants of the VLP subunit (VP1) are constructed through the substitution of double cysteines at the VP1 pentamer interfaces, generating a group of VLPs with altered size distributions. One of the mutants, SS2 (L102C/P300C), specifically forms homogenous T = 1-like tiny VLPs of 24 ± 3 nm in diameter. Moreover, the stability of the SS2 VLPs is markedly enhanced compared with that of wildtype VLPs. The homogeneous self-assembly and stability enhancement of SS2 VLPs can be attributed to the new disulfide bonds contributed by Cys102 and Cys300, which are identified by mass spectrometry and explored by molecular dynamics simulations. Endocytosis inhibition assays indicate that SS2 VLPs, like the polymorphic wild-type VLPs, preserve the multipathway feature of cellular uptake. SS2 VLPs may serve as an evolved version of SV40 VLPs in future studies and applications. The findings of this work would be useful for the design and fabrication of VLP-based materials and devices.
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