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Crooks, R. O., Baxter, D., Panek, A. S., Lubben, A. T. and Mason, J. M., 2016. Deriving heterospecific self-assembling protein-protein interactions using a computational interactome screen. Journal of Molecular Biology, 428 (2, Part A), pp. 385-398. Cheruvara, H., Allen-Baume, V. L., Kad, N. M. and Mason, J. M., 2015. Intracellular screening of a peptide library to derive a potent peptide inhibitor of α-synuclein aggregation. Journal of Biological Chemistry, 290, pp. 7426-7435. Mason, J. M. and Fairlie, D. P., 2015. Toward peptide-based inhibitors as therapies for Parkinson's disease. Future Medicinal Chemistry, 7 (16), pp. 2103-2105. Baxter, D., Ullman, C. and Mason, J., 2014. Library construction, selection and modification strategies to generate therapeutic peptide-based modulators of protein-protein interactions. Future Medicinal Chemistry, 6 (18), p. 2073. Acerra, N., Kad, N. M., Cheruvara, H. and Mason, J. M., 2014. Intracellular selection of peptide inhibitors that target disulphide-bridged Aβ42 oligomers. Protein Science, 23 (9), pp. 1262-1274. Acerra, N., Kad, N. M., Griffith, D. A., Ott, S., Crowther, D. C. and Mason, J. M., 2014. Retro-inversal of intracellular selected β-amyloid-interacting peptides:Implications for a novel Alzheimer’s disease treatment. Biochemistry, 53 (13), pp. 2101-2111. Acerra, N., Kad, N. M. and Mason, J. M., 2013. Combining intracellular selection with protein-fragment complementation to derive Aβ interacting peptides. Protein Engineering Design and Selection, 26 (7), pp. 463-470. Rao, T., Ruiz-Gómez, G., Hill, T. A., Hoang, H. N., Fairlie, D. P. and Mason, J. M., 2013. Truncated and helix-constrained peptides with high affinity and specificity for the cFos coiled-coil of AP-1. PLoS ONE, 8 (3), e59415. Mason, J. M., Bendall, D. S., Howe, C. J. and Worrall, J. A. R., 2012. The role of a disulfide bridge in the stability and folding kinetics of Arabidopsis thaliana cytochrome c6A. Biochimica Et Biophysica Acta-Proteins and Proteomics, 1824 (2), pp. 311-318. Crooks, R. O., Rao, T. and Mason, J. M., 2011. Truncation, randomization, and selection:Generation of a reduced length c-Jun antagonist that retains high interaction stability. Journal of Biological Chemistry, 286 (34), pp. 29470-29479. Worrall, J. A. R. and Mason, J. M., 2011. Thermodynamic analysis of Jun-Fos coiled coil peptide antagonists. FEBS Journal, 278 (4), pp. 663-672. Mason, J. M., 2010. Design and development of peptides and peptide mimetics as antagonists for therapeutic intervention. Future Medicinal Chemistry, 2 (12), pp. 1813-1822. Mason, J. M., 2009. Electrostatic contacts in the activator protein-1 coiled coil enhance stability predominantly by decreasing the unfolding rate. FEBS Journal, 276 (24), pp. 7305-7318. Mason, J. M., Hagemann, U. B. and Arndt, K. M., 2009. Role of hydrophobic and electrostatic interactions in coiled coil stability and specificity. Biochemistry, 48 (43), pp. 10380-10388. Mason, J. M., Muller, K. M. and Arndt, K. M., 2009. Peptides tailored to interfere with protein interaction and function. Chimica Oggi-Chemistry Today, 27 (2), pp. 47-50. Mason, J. M., Müller, K. M. and Arndt, K. M., 2008. iPEP:Peptides designed and selected for interfering with protein interaction and function. Biochemical Society Transactions, 36 (6), pp. 1442-1447. Hagemann, U. B., Mason, J. M., Müller, K. M. and Arndt, K. M., 2008. Selectional and mutational scope of peptides sequestering the Jun–Fos coiled-coil domain. Journal of Molecular Biology, 381 (1), pp. 73-88. Willemsen, T., Hagemann, U. B., Jouaux, E. J., Stebel, S. C., Mason, J. M., Muller, K. M. and Arndt, K. M., 2008. Protein engineering. In: Walker, J. M. and Rapley, R., eds. Molecular Biomethods Handbook, 2nd ed. Totowa, U. S. A.: Humana Press, pp. 587-631.