Paulson Laboratory
Nahid Razi, Ph.D.

The Scripps Research Institute
10550 North Torrey Pines Road, CB-216
La Jolla, CA 92037
858-784-7539(phone)
858-784-7542 (fax)
e-mail: nrazi@scripps.edu
ACADEMIC MERITS:

Ph. D. Medical Science, Uppsala University, Sweden, 1995
M. Sc. Biochemistry, University of Iowa, USA, 1984


EMPLOYMENTS:

2008- present   Director for Carbohydrate Synthesis / Protein Expression Core,  TSRI, San Diego, CA
2001-2008  Associate Director for Carbohydrate Synthesis / Protein Expression Core,  TSRI, San Diego, CA
2000-2001  Researcher, Department of Surgery, UCSD, San Diego, CA
1998-2000  Research director, Paik-Inje Memorial Institute, San Diego, CA
1995-1998  Post doctoral, Immuno-glycobiology, Cancer Center, UCSD, San Diego, CA
1988-1989  Research scientist in Molecular Biology, Uppsala University
1984-1988  Lecturer of Biochemical Genetics, School of Medicine, Tehran University


AWARDS  AND  SCHOLARSHIPS:

1998   Grant Award: "California Cancer Research Program", US
1997   Grant Award: "Cure for Lymphoma Foundation", US
1995   Grant Award: "Polysaccharide Research AB", Sweden
1990   Scholarship: "Uppsala University"
1978   First Rank Student Award: "Tehran University"


PUBLICATIONS:

Feinberg, H., Taylor, M., Razi, N., McBride, R., Knirel, Y., Graham, S., Drickamer, K., Weis, W. (2010) Structural Basis for Langerin Recognition of Diverse Pathogen and Mammalian Glycans through a Single Binding Site. J. Mol. Biol. In press

Peng, W., Pranskevich, J., Nycholat, C., Gilbert, M., Wakarchuk, W., Paulson, J.C., Razi, N. (2010) Enzymatic Synthesis of Poly-N-Acetyllactosamine (Pln) Derivatives on Branched Glycans for the CFG Glycan Array. Glycobiology. 51: 1465

Niemietz, M., Razi, N., Paulson, J.C., and Unverzagt, C. (2010) Chemoenzymatic Synthesis of Tetraantennary Bisected Core Fucosylated N-glycan Derivatives for the CFG Glycan Array. International Carb. Symposium publication. A-P2-072

Razi, N., Mcbride, R., Peng, W., Pranskevich, J., Rangarajan, J., Paulson, J.C. (2010) Characteristics of the CFG Printed Glycan Microarray V5.0- Final Glue-Grant Funded. Glycobiology. 68: 1470

Blixt, O. and Razi, N. (2008) Enzymatic Synthesis with Transferases Glycoscience, (Ed. B. Fraser-Reid) in Glycoscience, Chemistry and Chemical Biology, Springer-Verlag Berlin Heidelberg New York.

Blixt, O., Allin, K., Bohorov, O., Liu, X., Andersson-Sand, H., Hoffman, J. and Razi, N. (2008) Glycan microarrays for screening sialyltransferase specificities. Glycoconj. J. 25(1), 59-68.

Vasiliu, D., Razi, N., Zhang, Y., Jacobsen, N., Allin, K., Liu, X., Hoffmann, J., Bohorov, O. and Blixt, O. (2006) Large scale chemoenzymatic synthesis of blood group and tumor-associated poly-N-acetyllactosamine antigens. Carbohydr Res 341, 1447-1457.

Blixt, O. and Razi, N. (2006) Chemoenzymatic synthesis of glycan libraries. Methods Enzymol. 415, 137-53.

Blixt, O., Vasiliu, D., Allin, K., Jacobsen, N., Warnock, D., Razi, N., Paulson, J. Benatchez, S., Gilbert, M., and Wakarchuck, W. (2005) Chemoenzymatic synthesis of 2-azidoethyl-ganglio-oligosaccharides GD3, GT3, GM2, GD2, GT2, GM1, and GD1a, Carbohydrtae research, 340, 1963-1972

Westerklind, U., Hagback, P., Tidback, B., Wiik, L., Blixt, O., Razi, N., and Norberg, T. (2005) Synthesis of deoxy and acylamino derivatives of lactose and use of these for probing the active site of Neisseria meningitides N-acetylglucosaminyltransferase. Carbohydrate Research 340, 221-233.

Blixt, O., and Razi, N. (2004) Stategies for synthesis of an oligosaccharide library using a chemo-enzymatic approach. In synthesis of carbohydrate through biotechnology. ACS Symposium series 873. P.G. Wang and Y. Ichikawa 93-112

Blixt, O. Head, S., Mondala, T., Scanlan, C., Huflejt, M.E., Alvarez R., Bryan M.C., Fazio, F., Calarese, D., Stevens, J., Razi, N., Stevens, D.J., Skehel, J.J., van Die, I., Burton, D.R., Wilson, I.A, Cummings, R., Bovin, N., Wong, DC.H., and Paulson, J.C. (2004) Printed covalent glycan array for ligand binding proteins. Glycobiol.(13):846

Razi, N., and Varki, A. (1999) Cyptic sialic acid binding lectins in blook leukocytes can be unmasked my sialidase treatment or cellular activation. Glycobiol 9 (11):1225-1234

Varki, A., Brinkman-van der Linden, E., and Razi, N., (1998) SIGLECS: An expanding family of sialic acid binding I-type lectins with distinct expression patterns and complex functional regulation. International Carbohydrate Symposium, CP059

Razi, N., and Varki, A. (1998) Masking and Unmasking of CD22 lectin function in resting and activated B-Lymphocytes Proc. Natl. Acad.Sci USA 95:7469-7474

Razi, N, Varki, A., (1997) Regulation of the lectin function of CD22 during lymphocyte activation. Glycobiol., 7: 1038

Razi, N., Varki, A., (1997) Masking and unmaskin of the sialic acid binding lection function of CD22 during B Lymphocyte development and activation. Blood, 90, 455a

Razi, N., and Lindahl, U., (1995) Biosynthesis of heparin/heparan sulfate. The D-glucasomminyl 3-O-sulfotransferase reaction; target and inhibitor saccharides. J. Biol. Chem. 270:11267-11275

Razi, N., Feyzi, E., Bjrk, I., Naggi, A., Casu, B., and Lindahl, U. (1995) Structural and functional properties of heparin analogs obtained by chemical sulphation of E. coli K5 capsular polysaccharide. Biochem J., 309:465-475

Razi, N., Kreuger, J., Lindahl, B., Lay, L., Panza, L., Russo, G., and Lindahl, U. (1995) Indentification of O-sulfate substituents on D-glucurionic acid units in heparin-related glycosaminoglycans using novel synthetic disaccharide standards. Glycobiol. 5:807-811

Razi N., (1995) Chemical and Enzymatic O-sulfation of Heparin-related polysaccharides. Functional and Regulatory Aspects. Uppsala University Press.

Casu, B., Grazioli, G., Razi, N., Guerrini, M., Naggi, A., Torri, G., Oreste, P., Tursi, F., Zoppetti, G., and Lindahl, U., (1994) Heparin-like compounds prepared by chemical modification of capsular polysaccharide from E. coli K5. Carbohydr. Res. 263, 271-284

Casu, B., Grazioli, G., Hannesson, H., Jann, B., Jann, K., Lindahl, U., Naggi, A., Oreste P., Razi, N., Torri, G., Tursi, F., and Zoppeti, G. (1994) Biologically active, heparan sulfate-like species by combines chemical and enzymatic modification of the E.coli polysaccharide K5. Carbohydr. Lett., 1,107-114


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