2022
DOI: 10.1021/acs.bioconjchem.2c00030
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Engineering Self-Assembling Protein Nanoparticles for Therapeutic Delivery

Abstract: Despite remarkable advances over the past several decades, many therapeutic nanomaterials fail to overcome major in vivo delivery barriers. Controlling immunogenicity, optimizing biodistribution, and engineering environmental responsiveness are key outstanding delivery problems for most nanotherapeutics. However, notable exceptions exist including some lipid and polymeric nanoparticles, some virus-based nanoparticles, and nanoparticle vaccines where immunogenicity is desired. Self-assembling protein nanopartic… Show more

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Cited by 47 publications
(38 citation statements)
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“…Simple ferritin nanoparticle constructs are successfully produced in E. coli and then purified, but bacteria lack the ability to express glycosylated proteins and/or complex antigens. Thus, modified ferritin nanoparticles that require mammalian post-translational modifications must be produced in eukaryotic cells [ 73 ]. The simple recombinant ferritins derived from bacteria are typically synthesized by transforming the cells with vectors that express H and/or L subunits under a strong and inducible promotor [ 74 ].…”
Section: Preparation Of Ferritin Nanoparticlesmentioning
confidence: 99%
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“…Simple ferritin nanoparticle constructs are successfully produced in E. coli and then purified, but bacteria lack the ability to express glycosylated proteins and/or complex antigens. Thus, modified ferritin nanoparticles that require mammalian post-translational modifications must be produced in eukaryotic cells [ 73 ]. The simple recombinant ferritins derived from bacteria are typically synthesized by transforming the cells with vectors that express H and/or L subunits under a strong and inducible promotor [ 74 ].…”
Section: Preparation Of Ferritin Nanoparticlesmentioning
confidence: 99%
“…A protein of interest (POI) may be conjugated to ferritin's surface through genetic fusion of the gene encoding the POI to the N-terminal end of ferritin subunits, which are exposed to the protein's outer surface, using established recombinant DNA technologies for subsequent production in a chosen expression system [ 115 ]. From the expression of simple peptides to complex trimers, genetic fusion of POI on ferritin's external surface has had wide applications in the field of vaccine development, including the search for vaccines against influenza [ [116] , [117] , [118] ] Epstein-Barr virus [ 119 ], hepatitis C [ 73 , 120 , 121 ], HIV-1 [ 73 , 122 ], Lyme [ 123 ], RSV [ 124 ], and SARS-CoV-2 [ [125] , [126] , [127] , [128] , [129] , [130] , [131] , [132] , [133] ] which will be discussed in a later section. A pitfall to expressing a protein of interest on ferritin's exterior through genetic fusion, however, is that care must be taken to recombinantly express antigens in a way that does not impair their stability or conformation, nor impair ferritin's inter-subunit interactions during the self-assembly process [ 75 ].…”
Section: Exterior Modificationsmentioning
confidence: 99%
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“…11−13 These and many past, current, and future innovations in bioconjugates coupled with directed evolution, artificial intelligence, and automation is shepherding in a new era for improving global healthcare, agriculture, and the environment. 14,15 I am incredibly grateful and very excited to be a part of this growing field, community, and journal as the next leader of Bioconjugate Chemistry, a leading venue for publication of transformative research at the nexus of chemical and biological science and engineering. Along with publication, building trust through inclusive communication across our global Bioconjugate Chemistry community is an important effort that is aligned with the journal and my leadership goals.…”
mentioning
confidence: 99%