Phage as templates for hybrid materials and mediators for nanomaterial synthesis

Merzlyak, Anna; Lee, Seung‐Wuk

doi:10.1016/j.cbpa.2006.04.008

Cited by 131 publications

(98 citation statements)

References 43 publications

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“…Furthermore, each phage is capped by five p3 and p6 subunits on one end, and by five p7 and p9 subunits at the other end. [17][18][19][20][21] Among the sequences for the major and minor coat proteins, those for p3, p8, and p9 are particularly amenable for genetic modification for the consequent expression of recombinant coat protein subunits on the surface of the filamentous phage. Specifically, up to three different types of peptides can be expressed on the surface via corresponding modifications to the p3, p8, and p9 sequences.…”

Section: Filamentous Bacteriophages As Biomedical Nanoprobesmentioning

confidence: 99%

Nanoscale bacteriophage biosensors beyond phage display

Lee¹,

Song²,

Hwang³

et al. 2013

IJN

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Section: Filamentous Bacteriophages As Biomedical Nanoprobesmentioning

confidence: 99%

Nanoscale bacteriophage biosensors beyond phage display

Lee¹,

Song²,

Hwang³

et al. 2013

IJN

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“…Ag, Au, Pd, Gd, Ti, Co/Pt and Fe/Pt, oxides of Si, Fe, Ti, Zn, Sn, Ge, Mn, Cr, Co, Pb, sulfides of Zn, Cd, Pb, selenides of Cd, Zn, arsenides of Ga (pure and doped), zeolites, simple salts including CaCO 3 , and other materials such as fullerenes, carbon nanotubes and polymers. [62][63][64][66][67][68][69][70][71][72][73][74][75][76][77][78][79][80][81][82][83][84][85] Recent reviews have summarised the sequences of various peptides binding inorganic materials. 18,63 The use of combinatorial methods such as this could also be used to deduce useful information such as predictive rules governing the interfacial interactions between minerals and biomolecules that could be applied to a variety of other materials systems.…”

Section: 63-65mentioning

confidence: 99%

Interactions of biomolecules with inorganic materials: principles, applications and future prospects

Patwardhan

Perry

2007

J. Mater. Chem.

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The goal of this article is to overview the current understanding of biomolecule-inorganic materials interactions; to identify the 'rules' that govern interaction; to highlight the drawbacks of the present approaches and outline future challenges and opportunities.Please check this proof carefully. Our staff will not read it in detail after you have returned it. Translation errors between word-processor files and typesetting systems can occur so the whole proof needs to be read. Please pay particular attention to: tabulated material; equations; numerical data; figures and graphics; and references. If you have not already indicated the corresponding author(s) please mark their name(s) with an asterisk. Please e-mail a list of corrections or the PDF with electronic notes attached -do not change the text within the PDF file or send a revised manuscript.Please bear in mind that minor layout improvements, e.g. in line breaking, table widths and graphic placement, are routinely applied to the final version.We will publish articles on the web as soon as possible after receiving your corrections; no late corrections will be made.Please return your final corrections, where possible within 48 hours of receipt, by e-mail to: proofs@rsc.org Electronic (PDF) reprints will be provided free of charge to the corresponding author. Enquiries about purchasing paper reprints should be addressed via: http://www.rsc.org/Publishing/ReSourCe/PaperReprints/. Costs for reprints are below: Interactions between inorganic materials and biomolecules at the molecular level, although complex, are commonplace. Examples include biominerals, which are, in most cases, facilitated by and in contact with biomolecules; implantable biomaterials; and food and drug handling. The effectiveness of these functional materials is dependant on the interfacial properties i.e. the extent of molecular level 'association' with biomolecules. The goal of this overview is four-fold: to present biomolecule-inorganic materials interactions and our current understanding using selected examples; to elaborate on approaches that have been used to expose the mechanisms underpinning such interactions; to identify the 'rules' or 'guiding principles' that govern interactions that could be used to explain and hence predict behaviour; and finally to highlight the drawbacks of the present approaches and outline future challenges and opportunities. Reprint costs

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“…25 The viral capsid is aligned along the shaft and is composed of 2,700 copies of pVIII and ~5 copies of minor coat proteins pIII, pVI, pIX, and pVII located at either end. 21,22 The 50-residue pVIII (98% by mass) is composed of three distinct domains, namely, a negatively charged hydrophilic N-terminal domain (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20), an intermediate hydrophobic domain (21)(22)(23)(24)(25)(26)(27)(28)(29)(30)(31)(32)(33)(34)(35)(36)(37)(38)(39), and a positively charged domain (40)(41)(42)(43)(44)(45)(46)…”

Section: M13 Phagementioning

confidence: 99%

“…Owing to their unique nanoscopic structures capable of displaying genetically programmable surface peptides, M13 bacteriophage (phage) has drawn attention as a powerful bionanomaterial with the advent of bionanotechnology. 2 The unique advantages of phages over conventional bionanomaterials can be easily exploited for genetic information and biomimetic structure, which led to the development of various electronic and medical materials with precise molecular-level control. The biological advantages of phages such as evolution, specific recognition, and self-replication can be enhanced through genetic and chemical engineering.…”

Section: Introductionmentioning

confidence: 99%

Chemical modulation of M13 bacteriophage and its functional opportunities for nanomedicine

Chung¹,

Lee²,

Yoo³

2014

IJN

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M13 bacteriophage (phage) has emerged as an attractive bionanomaterial owing to its genetically tunable surface chemistry and its potential to self-assemble into hierarchical structures. Furthermore, because of its unique nanoscopic structure, phage has been proposed as a model system in soft condensed physics and as a biomimetic building block for structured functional materials. Genetic engineering of phage provides great opportunities to develop novel nanomaterials with functional surface peptide motifs; however, this biological approach is generally limited to peptides containing the 20 natural amino acids. To extend the scope of phage applications, strategies involving chemical modification have been employed to incorporate a wider range of functional groups, including synthetic chemical compounds. In this review, we introduce the design of chemoselective phage functionalization and discuss how such a strategy is combined with genetic engineering for a variety of medical applications, as reported in recent literature.

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Phage as templates for hybrid materials and mediators for nanomaterial synthesis

Cited by 131 publications

References 43 publications

Nanoscale bacteriophage biosensors beyond phage display

Nanoscale bacteriophage biosensors beyond phage display

Interactions of biomolecules with inorganic materials: principles, applications and future prospects

Chemical modulation of M13 bacteriophage and its functional opportunities for nanomedicine

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Phage as templates for hybrid materials and mediators for nanomaterial synthesis

Cited by 131 publications

References 43 publications

Nanoscale bacteriophage biosensors beyond phage display

Nanoscale bacteriophage biosensors beyond phage display

Interactions of biomolecules with inorganic materials: principles, applications and future prospects

Chemical modulation of M13 bacteriophage and&nbsp;its functional opportunities for nanomedicine

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Chemical modulation of M13 bacteriophage and its functional opportunities for nanomedicine