Filipe Natalio

Sponge spicules as blueprints for the biofabrication of inorganic–organic composites and biomaterials

While most forms of multicellular life have developed a calcium-based skeleton, a few specialized organisms complement their body plan with silica. However, of all recent animals, only sponges (phylum Porifera) are able to polymerize silica enzymatically mediated in order to generate massive siliceous skeletal elements (spicules) during a unique reaction, at ambient temperature and pressure. During this biomineralization process (i.e., biosilicification) hydrated, amorphous silica is deposited within highly specialized sponge cells, ultimately resulting in structures that range in size from micrometers to meters. Spicules lend structural stability to the sponge body, deter predators, and transmit light similar to optic fibers. This peculiar phenomenon has been comprehensively studied in recent years and in several approaches, the molecular background was explored to create tools that might be employed for novel bioinspired biotechnological and biomedical applications. Thus, it was discovered that spiculogenesis is mediated by the enzyme silicatein and starts intracellularly. The resulting silica nanoparticles fuse and subsequently form concentric lamellar layers around a central protein filament, consisting of silicatein and the scaffold protein silintaphin-1. Once the growing spicule is extruded into the extracellular space, it obtains final size and shape. Again, this process is mediated by silicatein and silintaphin-1, in combination with other molecules such as galectin and collagen. The molecular toolbox generated so far allows the fabrication of novel micro- and nanostructured composites, contributing to the economical and sustainable synthesis of biomaterials with unique characteristics. In this context, first bioinspired approaches implement recombinant silicatein and silintaphin-1 for applications in the field of biomedicine (biosilica-mediated regeneration of tooth and bone defects) or micro-optics (in vitro synthesis of light waveguides) with promising results.

Au@MnO Nanoflowers: Hybrid Nanocomposites for Selective Dual Functionalization and Imaging

Recently, the development of hybrid nanostructures consisting of various materials has attracted considerable interest. The assembly of different nanomaterials with specific optical, magnetic, or electronic properties to multicomponent composites can change and even enhance the properties of the individual constituents. Specifically tuning the structure and interface interactions within the nanocomposites has resulted in novel platforms of materials that may lead the way to various future technologies, such as synchronous biolabeling, protein separation and detection, heterogeneous catalysis, and multimodal imaging in biomedicine. Of the various kinds of nanomaterials, gold nanorods show an unusually high polarizability at optical frequencies arising from the excitation of localized surface-plasmon resonances (LSPRs). Furthermore, gold nanorods have promising therapeutic properties as hyperthermal agents because the local temperature around the gold nanorods can be increased by laser illumination through the tunable surface plasmon bands in the near infrared (NIR) region. Using NIR radiation for hyperthermal therapy is beneficial because of the low absorption and low scattering by blood and tissue in this spectral range. Magnetic nanoparticles constitute another major class of nanomaterials that have attracted much research effort over the past decades. In particular, exchange-coupled magnetic nanocomposites, such as antiferromagnetic/ferromagnetic core–shell nanoparticles, such as MnO/Mn3O4, have magnetic properties that are quite different from those of the individual components. Concerning biomedical applications, superparamagnetic nanoparticles are attractive as contrast agents for magnetic resonance imaging (MRI). The majority of nanoparticles that have been investigated in this field comprise iron oxides (Fe3O4, g-Fe2O3), which are known to shorten the transverse (or spin–spin) relaxation time T2. [11] Recently, manganese oxide nanoparticles (MnO NPs) have been shown to be interesting candidates as contrast agents for shortening of the longitudinal (or spin-lattice) relaxation time T1. [12] Consequently, a nanoparticulate system containing both an optically active plasmonic gold unit and a magnetically active MnO component would be advantageous for simultaneous optical and MRI detection. Although considerable research efforts have been put into the chemical design of suitable surface ligands, one of the major obstacles for biocompatible applications remains the lack of surface addressability. Therefore, a nanocomposite made up of individually addressable Au and MnO domains offers two functional surfaces for the attachment of different kinds of molecules, thus increasing both diagnostic and therapeutic potential. Furthermore, the size of either of the two components can be varied to optimize the magnetic and optical properties. Herein we present the successful synthesis of Au@MnO nanocomposites consisting of both paramagnetic MnO NPs and Au crystallites followed by separate surface functionalization of both domains with fluorescent ligands. Scheme 1 depicts a functionalized Au@MnO nanoflower with selective attachment of catechol anchors to the metal oxide petals and thiol anchors to the gold core. The nanoflowers were synthesized by decomposition of manganese acetylacetonate [Mn(acac)2] in diphenyl ether in the presence of preformed Au NPs (“seeds”), with oleic acid and oleylamine as surfactants, following a similar procedure for the preparation of Au@Fe3O4 heteroparticles by Sun et al. [15] The [*] T. D. Schladt, Dr. M. I. Shukoor, K. Schneider, Dr. M. N. Tahir, O. K hler, Prof. Dr. W. Tremel Institut f r Anorganische Chemie und Analytische Chemie Johannes-Gutenberg-Universit t Duesbergweg 10–14, 55099 Mainz (Germany) Fax: (+49)6131-39-25605 E-mail: tremel@uni-mainz.de

Controlled synthesis of linear and branched Au@ZnO hybrid nanocrystals and their photocatalytic properties

Colloidal Au@ZnO hybrid nanocrystals with linear and branched shape were synthesized. The number of ZnO domains on the Au seeds can be controlled by the solvent mixture. Imidazole-functionalized Au@ZnO hybrid nanocrystals were soluble in water and exhibited a greatly enhanced photocatalytic activity compared to ZnO nanocrystals. The pristine heterodimeric NPs were characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), and UV-Vis spectroscopy.

Highly soluble multifunctional MnO nanoparticles for simultaneous optical and MRI imaging and cancer treatment using photodynamic therapy

Superparamagnetic MnO nanoparticles were functionalized using a hydrophilic ligand containing protoporphyrin IX as photosensitizer. By virtue of their magnetic properties these nanoparticles may serve as contrast enhancing agents for magnetic resonance imaging (MRI), while the fluorescent target ligand protoporphyrin IX allows simultaneous tumor detection and treatment by photodynamic therapy (PDT). Caki-1 cells were incubated with these nanoparticles. Subsequent exposure to UV light lead to cell apoptosis due to photoactivation of the photosensitizer conjugated to the nanoparticles. This method offers great diagnostic potential for highly proliferative tissues, including tumors. In addition, it is an efficient platform that combines the advantages of a biocompatible photosensitizer with the possibility for MRI monitoring due to the magnetic properties of the highly soluble functionalized manganese oxide nanoparticles.

The role of the silicatein-α interactor silintaphin-1 in biomimetic biomineralization ☆

Biosilicification in sponges is initiated by formation of proteinaceous filaments, predominantly consisting of silicateins. Silicateins enzymatically catalyze condensation of silica nanospheres, resulting in symmetric skeletal elements (spicules). In order to create tailored biosilica structures in biomimetic approaches it is mandatory to elucidate proteins that are fundamental for the assembly of filaments. Silintaphin-1 is a core component of modularized filaments and also part of a spicule-enfolding layer. It bears no resemblance to other proteins, except for the presence of an interaction domain that is fundamental for its function as scaffold/template. In the presence of silicatein silintaphin-1 facilitates the formation of in vitro filaments. Also, it directs the assembly of gamma-Fe(2)O(3) nanoparticles and surface-immobilized silicatein to rod-like biocomposites, synthetic spicules. Thus, silintaphin-1 will contribute to biomimetic approaches that pursue a controlled formation of patterned biosilica-based materials. Its combination with gamma-Fe(2)O(3) nanoparticles and immobilized silicatein will furthermore inspire future biomedical applications and clinical diagnostics.

Bioengineering of the silica-polymerizing enzyme silicatein-α for a targeted application to hydroxyapatite

Since its discovery, numerous biotechnological approaches have aimed to explore the silica-polymerizing catalytic activity of the enzyme silicatein. In vivo, silicatein catalyzes polymerization of amorphous silica nanospheres from soluble precursors. In vitro, it directs the formation of nanostructured biosilica. This is of interest for various applications that strive to benefit from both the advantages of the biological system (i.e., silica synthesis under physiological conditions) and the cell mineralization-stimulating effect of biosilica. However, so far immobilization of silicatein has been hampered by the complex multistep procedure required. In addition, the chemical surface modifications involved not only restrict the choice of carrier materials but also render application of silicatein to hydroxyapatite (HA) of mineralized tissue impossible. Here we describe the bioengineering of silicatein, adapted for application in the fields of bone regeneration, tissue engineering, and dental care. Inspired by Glu-rich sequences of mammalian proteins that confer binding affinity to HA, a novel protein-tag was developed, the Glu-tag. Following expression of Glu-tagged silicatein, the HA-binding capacity of the enzyme is demonstrated in combination with synthetic and dental HA. Furthermore, immobilized Glu-tagged silicatein catalyzes synthesis of biosilica coatings on both synthetic HA nanofibrils and dental HA. Hence, Glu-tagged silicatein reveals a considerable biomedical potential with regenerative and prophylactic implementations.

Multifunctional superparamagnetic MnO@SiO2 core/shell nanoparticles and their application for optical and magnetic resonance imaging

Highly biocompatible multifunctional nanocomposites consisting of monodisperse manganese oxide nanoparticles with luminescent silica shells were synthesized by a combination of w/o-microemulsion techniques and common sol–gel procedures. The nanoparticles were characterized by TEM analysis, powder XRD, SQUID magnetometry, FT-IR, UV/vis and fluorescence spectroscopy and dynamic light scattering. Due to the presence of hydrophilic poly(ethylene glycol) (PEG) chains on the SiO2 surface, the nanocomposites are highly soluble and stable in various aqueous solutions, including physiological saline, buffer solutions and human blood serum. The average number of surface amino groups available for ligand binding on the particles was determined using a colorimetric assay with fluorescein isothiocyanate (FITC). This quantification is crucial for the drug loading capacity of the nanoparticles. SiO2 encapsulated MnO@SiO2 nanoparticles were less prone to Mn-leaching compared to nanoparticles coated with a conventional bi-functional dopamine–PEG ligand. The presence of a silica shell did not change the magnetic properties significantly, and therefore, the MnO@SiO2 nanocomposite particles showed a T1 contrast with relaxivity values comparable to those of PEGylated MnO nanoparticles. The cytotoxicity of the MnO@SiO2–PEG/NH2 nanoparticles was evaluated using primary cells of the innate immune system with bone marrow-derived polymorphonuclear neutrophils (BM-PMNs) as import phagocytes in the first line of defence against microbial pathogens, and bone marrow-derived dendritic cells (BMDCs), major regulators of the adaptive immunity. MnO@SiO2–PEG/NH2 nanoparticles have an acceptable toxicity profile and do not interact with BMDCs as shown by the lack of activation and uptake.

Bioinspired synthesis of multifunctional inorganic and bio‐organic hybrid materials

Owing to their physical and chemical properties, inorganic functional materials have tremendous impacts on key technologies such as energy generation and storage, information, medicine, and automotive engineering. Nature, on the other hand, provides evolution‐optimized processes, which lead to multifunctional inorganic–bio‐organic materials with complex structures. Their formation occurs under physiological conditions, and is goverened by a combination of highly regulated biological processes and intrinsic chemical properties. Nevertheless, insights into the molecular mechanisms of biomineralization open up promising perspectives for bioinspired and biomimetic design and the development of inorganic–bio‐organic multifunctional hybrids. Therefore, biomimetic approaches may disclose new synthetic routes under ambient conditions by integrating the concept of gene‐regulated biomineralization principles. The skeletal structures of marine sponges provide an interesting example of biosilicification via enzymatically controlled and gene‐regulated silica metabolism. Spicule formation is initiated intracellularly by a fine‐tuned genetic mechanism, which involves silica deposition in vesicles (silicassomes) under the control of the enzyme silicatein, which has both catalytic and templating functions. In this review, we place an emphasis on the fabrication of biologically inspired materials with silicatein as a biocatalyst.

Marine molecular biology: An emerging field of biological sciences

An appreciation of the potential applications of molecular biology is of growing importance in many areas of life sciences, including marine biology. During the past two decades, the development of sophisticated molecular technologies and instruments for biomedical research has resulted in significant advances in the biological sciences. However, the value of molecular techniques for addressing problems in marine biology has only recently begun to be cherished. It has been proven that the exploitation of molecular biological techniques will allow difficult research questions about marine organisms and ocean processes to be addressed. Marine molecular biology is a discipline, which strives to define and solve the problems regarding the sustainable exploration of marine life for human health and welfare, through the cooperation between scientists working in marine biology, molecular biology, microbiology and chemistry disciplines. Several success stories of the applications of molecular techniques in the field of marine biology are guiding further research in this area. In this review different molecular techniques are discussed, which have application in marine microbiology, marine invertebrate biology, marine ecology, marine natural products, material sciences, fisheries, conservation and bio-invasion etc. In summary, if marine biologists and molecular biologists continue to work towards strong partnership during the next decade and recognize intellectual and technological advantages and benefits of such partnership, an exciting new frontier of marine molecular biology will emerge in the future.

Phase separated Cu@Fe3O4 heterodimer nanoparticles from organometallic reactants

Cu@Fe3O4 heteroparticles with distinct morphologies were synthesized from organometallic reactants. The shape of the magnetic domains could be controlled by the solvent and reaction conditions. They display magnetic and optical properties that are useful for simultaneous magnetic and optical detection. After functionalization, the Cu@Fe3O4 heterodimers become water soluble. The morphology, structure, magnetic and optical properties of the as-synthesized heterodimer nanoparticles were characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), mossbauer spectroscopy, superconducting quantum interference device (SQUID) magnetometry, and dark field imaging. A special advantage of these heterodimers lies in the fact that the nanodomains of different composition can be used e.g. for the formation of nitric oxide (NO) through the Cu domain and heterodimer nanoparticles can be removed from the reaction mixture by means of the magnetic domain (Fe3O4).