A new analytical method to study the dissociation of the complexes between the oncosuppressor p53 and its negative modulators murine double-minute protein 2 (MDM2) or MDMX, is proposed. This technique is reliable to determine the dissociative power exerted by small molecules on the complex taking advantage of the appearance of migrating MDM2 or MDMX in a native polyacrylamide gel, when inhibitors are added to the complex mixture. Therefore, we propose this new approach to easily screen library of compounds, with potential pharmacological anticancer activity.
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Columbia Univ, Integrated Program Cellular Mol & Biomed Studies, New York, NY 10032 USAColumbia Univ, Integrated Program Cellular Mol & Biomed Studies, New York, NY 10032 USA
Klein, Alyssa M.
de Queiroz, Rafaela Muniz
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Columbia Univ, Dept Biol Sci, New York, NY 10027 USAColumbia Univ, Integrated Program Cellular Mol & Biomed Studies, New York, NY 10032 USA
de Queiroz, Rafaela Muniz
Venkatesh, Divya
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Columbia Univ, Dept Biol Sci, New York, NY 10027 USAColumbia Univ, Integrated Program Cellular Mol & Biomed Studies, New York, NY 10032 USA
Venkatesh, Divya
Prives, Carol
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Columbia Univ, Dept Biol Sci, New York, NY 10027 USAColumbia Univ, Integrated Program Cellular Mol & Biomed Studies, New York, NY 10032 USA