Changing the net charge from negative to positive makes ribonuclease Sa cytotoxic
- 1 October 2002
- journal article
- Published by Wiley in Protein Science
- Vol. 11 (10) , 2522-2525
- https://doi.org/10.1110/ps.0216702
Abstract
Ribonuclease Sa (pI = 3.5) from Streptomyces aureofaciens and its 3K (D1K, D17K, E41K) (pI = 6.4) and 5K (3K + D25K, E74K) (pI = 10.2) mutants were tested for cytotoxicity. The 5K mutant was cytotoxic to normal and v-ras-transformed NIH3T3 mouse fibroblasts, but RNase Sa and 3K were not. The structure, stability, and activity of the three proteins are comparable, but the net charge at pH 7 increases from -7 for RNase Sa to -1 for 3K and to +3 for 5K. These results suggest that a net positive charge is a key determinant of ribonuclease cytotoxicity. The cytotoxic 5K mutant preferentially attacks v-ras-NIH3T3 fibroblasts, suggesting that mammalian cells expressing the ras-oncogene are potential targets for ribonuclease-based drugs.Keywords
This publication has 20 references indexed in Scilit:
- The effect of net charge on the solubility, activity, and stability of ribonuclease SaProtein Science, 2001
- Differential Requirement for the Stress-Activated Protein Kinase/c-Jun NH2-Terminal Kinase in RNA Damage-Induced Apoptosis in Primary and in Immortalized FibroblastsMolecular Cell Biology Research Communications, 2000
- Onconase: An Unusually Stable ProteinBiochemistry, 2000
- Conformational Stability Is a Determinant of Ribonuclease A CytotoxicityJournal of Biological Chemistry, 2000
- A Ribonuclease A Variant with Low Catalytic Activity but High CytotoxicityPublished by Elsevier ,2000
- Purification of Ribonucleases Sa, Sa2, and Sa3 after Expression inEscherichia coliProtein Expression and Purification, 1997
- SOS-inducing ability of native and mutant microbial ribonucleasesMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1996
- Mechanism of Ribonuclease CytotoxicityJournal of Biological Chemistry, 1995
- A Study of the Intracellular Routing of Cytotoxic RibonucleasesPublished by Elsevier ,1995
- Catalytic activity of bovine seminal ribonuclease is essential for its immunosuppressive and other biological activitiesBiochemical Journal, 1995