7 results on '"Rodríguez-Vázquez, N."'
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2. cis-Platinum Complex Encapsulated in Self-Assembling Cyclic Peptide Dimers.
- Author
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Rodríguez-Vázquez, N., García-Fandiño, R., Aldegunde, M. J., Brea, J., Loza, M. I., Amorín, M., and Granja, J. R.
- Subjects
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CISPLATIN , *DIMERS , *CYCLIC peptides , *OVARIAN cancer , *CELL lines - Abstract
A new cyclic peptide dimer that encapsulates cisplatin complexes in its internal cavity is described. The resulting complex showed cytotoxic activity at A2780 ovarian cancer cell lines independent of acquired platinum resistance. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
3. Use of Smartphones to Increase Safe Sexual Behavior in Youths at Risk for HIV.
- Author
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Hernández-Torres JL, Benavides-Torres RA, Moreno-Monsiváis MG, Rodríguez-Vázquez N, Martínez-Cervantes R, and Cárdenas-Cortés AM
- Abstract
In Mexico, young people continue to experience problems due to a lack of correct and consistent condom use during sexual intercourse., Objective: to evaluate the effect of a randomized controlled clinical trial with the use of smartphones to increase safe sex intentions and safe sexual behavior., Methods: experimental design with two treatment groups with 177 young people who requested the rapid HIV test in a non-governmental organization in the city of Monterrey, Mexico. The experimental group was given Respect M-Health with the use of mobile devices; the control group was given similar counseling without the use of mobile technology and 8 pencil and paper instruments were used., Results: the effect of the experimental group was greater in safe sexual behavior reflected in the means at pre-test M=64.80 (SD=1.86), post-test M=85.33 (SD=1.54), and at 30 days M=87.40 (SD=1.52), and in the safe sex intentions factor at pre-test M=78.50 (SD=3.07), post-test M=94.70 (SD=2.46), and at 30 days M=95.74 (SD=2.29)., Conclusions: Smartphone use was an effective tool as a support to increase safe sexual behavior in youth., Competing Interests: Conflict of interests: The authors have declared that there is no conflict of interest.
- Published
- 2022
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- View/download PDF
4. Anion Recognition and Induced Self-Assembly of an α,γ-Cyclic Peptide To Form Spherical Clusters.
- Author
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Rodríguez-Vázquez N, Amorín M, Alfonso I, and Granja JR
- Abstract
A cyclic octapeptide composed of hydroxy-functionalized γ-amino acids folds in a "V-shaped" conformation that allows the selective recognition of anions such as chloride, nitrate, and carbonate. The process involves the simultaneous self-assembly of six peptide subunits and the recognition of four anions to form a tetrahedral structure, in which the anions are located at the corners of the resulting structure. Each anion is coordinated to three different peptides. The structure was fully characterized by several techniques, including NMR spectroscopy and X-ray diffraction, and the material was able to facilitate the transmembrane transport of chloride ions., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Published
- 2016
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5. Bioinspired Artificial Sodium and Potassium Ion Channels.
- Author
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Rodríguez-Vázquez N, Fuertes A, Amorín M, and Granja JR
- Subjects
- Carrier Proteins, Catalytic Domain, Cell Membrane, Macromolecular Substances, Models, Molecular, Protein Conformation, Potassium metabolism, Potassium Channels chemical synthesis, Potassium Channels metabolism, Sodium metabolism, Sodium Channels chemical synthesis, Sodium Channels metabolism
- Abstract
In Nature, all biological systems present a high level of compartmentalization in order to carry out a wide variety of functions in a very specific way. Hence, they need ways to be connected with the environment for communication, homeostasis equilibrium, nutrition, waste elimination, etc. The biological membranes carry out these functions; they consist of physical insulating barriers constituted mainly by phospholipids. These amphipathic molecules spontaneously aggregate in water to form bilayers in which the polar groups are exposed to the aqueous media while the non-polar chains self-organize by aggregating to each other to stay away from the aqueous media. The insulating properties of membranes are due to the formation of a hydrophobic bilayer covered at both sides by the hydrophilic phosphate groups. Thus, lipophilic molecules can permeate the membrane freely, while the small charged or very hydrophilic molecules require the assistance of other membrane components in order to overcome the energetic cost implied in crossing the non-polar region of the bilayer. Most of the large polar species (such as oligosaccharides, polypeptides or nucleic acids) cross into and out of the cell via endocytosis and exocytosis, respectively. Nature has created a series of systems (carriers and pores) in order to control the balance of small hydrophilic molecules and ions. The most important structures to achieve these goals are the ionophoric proteins that include the channel proteins, such as the sodium and potassium channels, and ionic transporters, including the sodium/potassium pumps or calcium/sodium exchangers among others. Inspired by these, scientists have created non-natural synthetic transporting structures to mimic the natural systems. The progress in the last years has been remarkable regarding the efficient transport of Na(+) and K(+) ions, despite the fact that the selectivity and the ON/OFF state of the non-natural systems remain a present and future challenge.
- Published
- 2016
- Full Text
- View/download PDF
6. Self-assembling α,γ-cyclic peptides that generate cavities with tunable properties.
- Author
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Rodríguez-Vázquez N, García-Fandiño R, Amorín M, and Granja JR
- Abstract
The design and synthesis of β-sheet-based self-assembling cyclic peptides with tunable cavities is described. The incorporation of a γ-amino acid with a hydroxyl group at C2 allows the incorporation of different groups that modify the internal properties of the resulting dimeric ensemble. These dimers can entrap different guests depending on the properties of the group at C2. The guest defines the geometry of the resulting aggregate.
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- 2016
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7. Membrane-targeted self-assembling cyclic peptide nanotubes.
- Author
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Rodríguez-Vázquez N, Ozores HL, Guerra A, González-Freire E, Fuertes A, Panciera M, Priegue JM, Outeiral J, Montenegro J, Garcia-Fandino R, Amorin M, and Granja JR
- Subjects
- Anti-Infective Agents pharmacology, Carboxylic Acids chemistry, Cell Membrane chemistry, Cell Membrane drug effects, Cycloparaffins chemistry, Escherichia coli drug effects, Escherichia coli growth & development, Hydrophobic and Hydrophilic Interactions, Ion Channels pharmacology, Ion Transport, Nanotubes toxicity, Pore Forming Cytotoxic Proteins pharmacology, Staphylococcus aureus drug effects, Staphylococcus aureus growth & development, Ulva drug effects, Ulva growth & development, Anti-Infective Agents chemistry, Ion Channels chemistry, Nanotubes chemistry, Peptides, Cyclic chemistry, Pore Forming Cytotoxic Proteins chemistry
- Abstract
Peptide nanotubes are novel supramolecular nanobiomaterials that have a tubular structure. The stacking of cyclic components is one of the most promising strategies amongst the methods described in recent years for the preparation of nanotubes. This strategy allows precise control of the nanotube surface properties and the dimensions of the tube diameter. In addition, the incorporation of 3- aminocycloalkanecarboxylic acid residues in the nanotube-forming peptides allows control of the internal properties of the supramolecular tube. The research aimed at the application of membrane-interacting self-assembled cyclic peptide nanotubes (SCPNs) is summarized in this review. The cyclic peptides are designed to interact with phospholipid bilayers to induce nanotube formation. The properties and orientation of the nanotube can be tuned by tailoring the peptide sequence. Hydrophobic peptides form transmembrane pores with a hydrophilic orifice, the nature of which has been exploited to transport ions and small molecules efficiently. These synthetic ion channels are selective for alkali metal ions (Na(+), K(+) or Cs(+)) over divalent cations (Ca(2+)) or anions (Cl(-)). Unfortunately, selectivity was not achieved within the series of alkali metal ions, for which ion transport rates followed the diffusion rates in water. Amphipathic peptides form nanotubes that lie parallel to the membrane. Interestingly, nanotube formation takes place preferentially on the surface of bacterial membranes, thus making these materials suitable for the development of new antimicrobial agents.
- Published
- 2014
- Full Text
- View/download PDF
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