prodigiosin and Cystic-Fibrosis

prodigiosin has been researched along with Cystic-Fibrosis* in 2 studies

Reviews

1 review(s) available for prodigiosin and Cystic-Fibrosis

ArticleYear
Small-molecule lipid-bilayer anion transporters for biological applications.
    Angewandte Chemie (International ed. in English), 2013, Jan-28, Volume: 52, Issue:5

    The development of small-molecule lipid-bilayer anion transporters for potential future use in channel replacement therapy for the treatment of diseases caused by dysregulation of anion transport (such as cystic fibrosis), and in treating cancer by perturbing chemical gradients within cells, thus triggering apoptosis, is an area of intense current interest. This Minireview looks at recent developments in the design of small-molecule transmembrane anion transporters and focuses on the progress so far in employing these compounds in biological systems.

    Topics: Anions; Antineoplastic Agents; Apoptosis; Cystic Fibrosis; Humans; Ion Transport; Lipid Bilayers; Neoplasms; Prodigiosin

2013

Other Studies

1 other study(ies) available for prodigiosin and Cystic-Fibrosis

ArticleYear
Small molecule anionophores promote transmembrane anion permeation matching CFTR activity.
    Scientific reports, 2018, 02-08, Volume: 8, Issue:1

    Anion selective ionophores, anionophores, are small molecules capable of facilitating the transmembrane transport of anions. Inspired in the structure of natural product prodigiosin, four novel anionophores 1a-d, including a 1,2,3-triazole group, were prepared. These compounds proved highly efficient anion exchangers in model phospholipid liposomes. The changes in the hydrogen bond cleft modified the anion transport selectivity exhibited by these compounds compared to prodigiosin and suppressed the characteristic high toxicity of the natural product. Their activity as anionophores in living cells was studied and chloride efflux and iodine influx from living cells mediated by these derivatives was demonstrated. These compounds were shown to permeabilize cellular membranes to halides with efficiencies close to the natural anion channel CFTR at doses that do not compromise cellular viability. Remarkably, optimal transport efficiency was measured in the presence of pH gradients mimicking those found in the airway epithelia of Cystic Fibrosis patients. These results support the viability of developing small molecule anionophores as anion channel protein surrogates with potential applications in the treatment of conditions such as Cystic Fibrosis derived from the malfunction of natural anion transport mechanisms.

    Topics: Animals; Anions; Cell Membrane; Cell Membrane Permeability; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Humans; Ion Transport; Ionophores; Prodigiosin; Tumor Cells, Cultured

2018