Sensor impedimétrico para la detección de bacterias patogénicas mediante péptidos antimicrobianos

Áccesit Congreso SIBB 2015La peri-implantitis, una inflamación causada por la formación del biofilm, es una de las causas más importantes de la fallida de los implantes en odontología. Por esto, la detección de bacterias patogénicas al inicio del proceso de formación de biofilms, representa una estrategia muy potente para la prevención de las infecciones en los implantes. Entre los diferentes métodos para la detección de bacterias patogénicas, los biosensores electroquímicos, especialmente los sistemas basados en impedancia (EIS), presentan una serie de ventajas como la miniaturización, la mejora en sensibilidad y el bajo coste. En este sentido, los péptidos antimicrobianos (AMPs), conocidos como componentes del sistema inmune y con actividad hacia las bacterias, pueden ser usados para desarrollar elementos de bioreconocimiento altamente efectivos. Por lo tanto, el objetivo de este estudio es la combinación del uso de EIS y la habilidad de los AMPs para obtener biosensores con alta sensibilidad, especificidad y límites de detección muy bajos para la detección de bacterias patogénicas.Peer ReviewedAward-winnin

Towards the cell-instructive bactericidal substrate:exploring the combination of nanotopographical features and integrin selective synthetic ligands

Engineering the interface between biomaterials and tissues is important to increase implant lifetime and avoid failures and revision surgeries. Permanent devices should enhance attachment and differentiation of stem cells, responsible for injured tissue repair, and simultaneously discourage bacterial colonization; this represents a major challenge. To take first steps towards such a multifunctional surface we propose merging topographical and biochemical cues on the surface of a clinically relevant material such as titanium. In detail, our strategy combines antibacterial nanotopographical features with integrin selective synthetic ligands that can rescue the adhesive capacity of the surfaces and instruct mesenchymal stem cell (MSC) response. To this end, a smooth substrate and two different high aspect ratio topographies have been produced and coated either with an avß3-selective peptidomimetic, an a5ß1-selective peptidomimetic, or an RGD/PHSRN peptidic molecule. Results showed that antibacterial effects of the substrates could be maintained when tested on pathogenic Pseudomonas aeruginosa. Further, functionalization increased MSC adhesion to the surfaces and the avß3-selective peptidomimetic-coated nanotopographies promoted osteogenesis. Such a dual physicochemical approach to achieve multifunctional surfaces represents a first step in the design of novel cell-instructive biomaterial surfaces.Peer ReviewedPostprint (published version

Strategies to inhibit tumour associated integrin receptors: rationale for dual and multi-antagonists

YesThe integrins are a family of 24 heterodimeric transmembrane cell surface receptors. Involvement in cell attachment to the extracellular matrix, motility, and proliferation identifies integrins as therapeutic targets in cancer and associated conditions; thrombosis, angiogenesis and osteoporosis. The most reported strategy for drug development is synthesis of an agent that is highly selective for a single integrin receptor. However, the ability of cancer cells to change their integrin repertoire in response to drug treatment renders this approach vulnerable to the development of resistance and paradoxical promotion of tumor growth. Here, we review progress towards development of antagonists targeting two or more members of the RGD-binding integrins, notably αvβ3, αvβ5, αvβ6, αvβ8, α5β1, and αIIbβ3, as anticancer therapeutics

Self-assembly of bioactive peptides, peptide conjugates, and peptide-mimetic materials

Molecular self-assembly is a multi-disciplinary field of research, with potential chemical and biological applications. One of the main driving forces of self-assembly is molecular amphiphilicity, which can drive formation of complex and stable nanostructures. Self-assembling peptide and peptide conjugates have attracted great attention due to their biocompatibility, biodegradability and biofunctionality. Understanding assembly enables the better design of peptide amphiphiles which may form useful and functional nanostructures. This review covers self-assembly of amphiphilic peptides and peptide mimetic materials, as well as their potential applications

Smallest peptoids with antiproliferative activity on human neoplastic cells.

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Increasing αvβ3 selectivity of the anti-angiogenic drug cilengitide by N-methylation

A subtle change: Structural changes upon amide bond methylation improve the selectivity of the anti-angiogenic drug Cilengitide, which after N-methylation at distinct positions discriminates between the closely related pro-angiogenic integrins αvβ3 and αvβ5 (see scheme). © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim