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Divalent Cation Mediated Binding of Oligonucleotides to Langmuir Monolayers of Charged Lipids

Year: 1996

Journal: Langmuir 1996, 12, 1879-1883, 20111221

Authors: David G. Rhodes and Jie Liu

Organizations: Department of Pharmaceutical Sciences, University of Connecticut School of Pharmacy, Storrs, Connecticut 06269-2092, and Pharmaceutics Division, College of Pharmacy, University of Texas at Austin, Austin, Texas 78717-1074

Antisense oligonucleotides inhibit the expression of complementary target sequences with extraordinary selectivity and thus have great potential for development of novel therapeutics in many critical areas, including cancer and infectious disease. However, the mechanism by which oligonucleotides pass through the cellmembraneand reach the site of action is not well understood. In this study, phospholipid monolayers were used as models of cell membranes. Using a Langmuir film balance, the effects of ions, oligonucleotides, and other polyions (polylysine) on the isotherms of phospholipid monolayers were determined. Differences were observed in the coexistence region between liquid expanded and condensed phases. These results indicate that calcium or other divalent cations may mediate interaction of oligonucleotides with DPPG or other anionic membrane components.