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Total synthesis of proteins for structural and functional studies
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Cox, V., Clarke, S., Czyzyk, T., Ansonoff, M., Nitsche, J., Hsu, M-S., Borsodi, A., Tömböly, Cs., Tóth, G., Hill, R., Pintar, J., Kitchen, I.: Autoradiography in opioid triple knock out mice reveals opioid receptor like binding of naloxone benzoylhydrazone., Neuropharmacology 48: 228-235, 2005 | Ioja, E., Tóth, G., Benyhe, S., Tourwé, D., Péter, A., Tömböly, Cs., Borsodi, A.: Opioid receptor binding characteristics and structure-activity studies of novel tetrapeptides in the TIPP (Tyr-Tic-Phe-Phe) series., Neurosignals 14: 317-328, 2005 | Van Rompaey, K., Ballet, S., Tömböly, Cs., De Wachter, R., Vanommeslaeghe, K., Biesemans, M., Willem, R., Tourwé, D.: Synthesis and evaluation of the β-turn properties of 4-amino-1,2,4,5-tetrahydro-2-benzazepin-3-ones and of their spirocyclic derivative., Eur. J. Org. Chem. 13: 2899-2911, 2006 | Botros, M., Hallberg, M., Johansson, T., Zhou, Q., Lindeberg, G., Frändberg, P-A., Tömböly, Cs., Tóth, G., Le Grevès, P., Nyberg, F.: Endomorphin-1 and endomorphin-2 differentially interact with specific binding sites for substance P (SP) aminoterminal SP1–7 in the rat spinal cord., Peptides 27: 753-759, 2006 | Tömböly, Cs., Tóth, G., Welker, E.: Maltóz-kötő fehérje módosítása kémiai ligációval., A Peptidkémiai Munkabizottság tudományos ülése, Balatonszemes, 2006. máj. 29-31., 2006 | Tömböly, Cs., Feytens, D., Tóth, G., Benyhe, S., Borsodi, A., Tourwé, D.: Design and synthesis of 4-amino-1,2,4,5-tetrahydro-2-benzazepine-3-one containing endomorphin-2 mimetics., pp 123-124 in 2nd International Congress Natural Peptides to Drugs, 18-21 April 2006, Zermatt, Switzerland, 2006 | Tóth, G., Ioja, E., Tömböly, Cs., Ballet, S., Tourwé, D., Péter, A., Martinek, T., Chung, N.N., Schiller, P.W., Benyhe, S., Borsodi, A.: B-Methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent d opioid antagonists., J. Med. Chem. 50: 328-333, 2007 | Tömböly, Cs., Welker, E.: Toward an improved protein ligation method for consecutive coupling of protein fragments, 32nd FEBS Congress, 2007 | Ballet, S., De Wachter, R., van Rompaey, K., Tömböly, Cs., Feytens, D., Tóth, G., Quartara, L., Cucchi, P., Meini, S., Tourwé, D.: Bradykinin analogs containing the 4-amino-2-benzazepin-3-one scaffold at the C-terminus, J. Pept. Sci. 13: 164-170, 2007 | Keresztes, A., Szűcs, M., Borics, A., E. Kövér, K., Forró, E., Fülöp, F., Tömböly, Cs., Péter, A., Páhi, A., Fábián, G., Murányi, M., Tóth, G.: New endomorphin analogues containing alicyclic beta-amino acids: influence on bioactive conformation and pharmacological profile, J. Med. Chem. 51: 4270-4279, 2008 | Botros, M., Johansson, T., Zhou, Q., Lindeberg, G., Tömböly, Cs., Tóth, G., Le Grevès, P., Nyberg, F., Hallberg, M.: Endomorphins interact with the substance P (SP) aminoterminal SP(1-7) binding in the ventral tegmental area of the rat brain, Peptides 29: 1820-1824, 2008 | Tömböly, Cs., Welker, E.: Improved expressed protein ligation method for consecutive coupling of polypeptide fragments, J. Pept. Sci. 14 S1: 183, 2008 | Tömböly, Cs., Welker, E.: Improved expressed protein ligation method for consecutive coupling of polypeptide fragments, Peptides 2008, 2008 | Tömböly, Cs., Ballet, S., Feytens, D., E. Kövér, K., Borics, A., Lovas, S., Al-Khrasani, M., Fürst, Zs., Tóth, G., Benyhe, S., Tourwé, D.: Endomorphin-2 with a β-turn backbone constraint retains the potent μ opioid receptor agonist properties, J. Med. Chem. 51: 173-177, 2008 |
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