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1.
Eur J Med Chem ; 158: 453-462, 2018 Oct 05.
Artículo en Inglés | MEDLINE | ID: mdl-30241012

RESUMEN

The demonstrated involvement of VEGF165/NRP-1 complex in pathological angiogenesis has catalyzed interest in blocking this interaction to combat angiogenesis dependent diseases. It was shown before that Lys-Pro-Pro-Arg is a fairly strong inhibitor of the VEGF165/NRP-1 interaction. Our current findings suggest that the side chain elongation of the Lys1 by branching it with additional homoarginine (Har) residue, to obtain Lys(Har)-Pro-Pro-Arg, allows more effective inhibition. Moreover, increasing the flexibility of the middle part of molecule, in particular with simultaneous introduction of additional interacting elements at the second or third position, produced compounds up to 30-fold more active (IC50 = 0.2 µM) than the heptapeptide ATWLPPR (A7R) which is one of the first peptide known as an effective antagonist of the VEGF165 binding to NRP-1 and in vivo decreases breast cancer angiogenesis and growth. Herein, we present also the structure-activity study of Lys(Har)-Pro-Pro-Arg, discussing the design, synthesis, inhibitory activity, proteolytic stability and molecular modeling of the prepared derivatives. For two of the most active analogs the high proteolytic stability was also observed. These studies provide the next step for elucidating the optimal structure of the small peptidic inhibitors of VEGF165/NRP-1 interaction that could serve as research tools or be prospective drug candidates.


Asunto(s)
Diseño de Fármacos , Neuropilina-1/metabolismo , Oligopéptidos/química , Oligopéptidos/farmacología , Mapas de Interacción de Proteínas/efectos de los fármacos , Factor A de Crecimiento Endotelial Vascular/metabolismo , Secuencia de Aminoácidos , Inhibidores de la Angiogénesis/sangre , Inhibidores de la Angiogénesis/química , Inhibidores de la Angiogénesis/metabolismo , Inhibidores de la Angiogénesis/farmacología , Humanos , Simulación del Acoplamiento Molecular , Oligopéptidos/sangre , Oligopéptidos/metabolismo , Unión Proteica/efectos de los fármacos
2.
ACS Appl Mater Interfaces ; 7(7): 3931-9, 2015 Feb 25.
Artículo en Inglés | MEDLINE | ID: mdl-25625378

RESUMEN

A novel inorganic nanocomposite material, called BOA, which has the form of small building blocks composed of gold nanoparticles embedded in a polyoxoborate matrix, is presented. It is demonstrated that cotton wool decorated with the BOA nanocomposite displays strong antibacterial activity toward both Gram-positive and -negative bacteria strains. Importantly, the modified cotton does not release any toxic substances, and the bacteria are killed upon contact with the fibers coated with the BOA. Toxicity tests show that the nanocomposite--in spite of its antiseptic properties--is harmless for mammalian cells. The presented method of surface modification utilizes mild, environmentally friendly fabrication conditions. Thus, it offers a facile approach to obtain durable nontoxic antiseptic coatings for biomedical applications.


Asunto(s)
Antibacterianos/química , Boratos/química , Oro/farmacología , Nanocompuestos/química , Animales , Antibacterianos/síntesis química , Antibacterianos/farmacología , Boratos/farmacología , Escherichia coli/efectos de los fármacos , Oro/química , Humanos , Staphylococcus aureus/efectos de los fármacos , Textiles/análisis , Textiles/microbiología , Lana/química , Lana/microbiología
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