Carrico:Publications

Carrico Lab at Stony Brook

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Publications

Carrico, I. S. (2008) A cysteine protease that cuts and pastes. Nat. Chem. Biol. 4, 525-526.

Carrico, I. S. (2008) Chemoselective protein modification: hitting the target. Chem. Soc. Rev. 37, 1423-1431.

Carrico, I. S.; Carlson, B.; Bertozzi, C. R. (2007) A genetically encodable aldehyde-tag for site-specific protein modification. Nat. Chem. Biol. 3, 321-322.

Carrico, I. S.; Ganguli, A.; Bertozzi, C. R. (2008) Proteomic profiling of glycoproteome subclasses with metabolic labeling. In preparation.

Laughlin, S. T.; Agard, N. A.; Baskin, J. M.; Carrico, I. S.; Chang, P. V.; Ganjuli, A. S.; Hangauer, M. J.; Lo, A.; Prescher, J. A.; Bertozzi, C. R. (2006) Metabolic labeling of glycans with azido sugars for visualization and glycoproteomics. Meth. Enz. 415, 230-250.

Carrico, I. S.; Heilshorn, S. A.; Mock, M. L.; Franck, C.; Ravichandran, G.; Tirrell, D. A. (2007) Lithographic patterning of intrinsically photoreactive cell-adhesive proteins. J. Am. Chem. Soc. 129, 4874-4875.

Wang, P.; Carrico, I. S.; Kirshenbaum, K.; Tang, Y.; Datta, D.; Mayo, S. L.; Tirrell, D. A. (2007) Engineering relaxed substrate specificity in E. coli phenylalanyl-tRNA synthetase to incorporate a diverse set of non-natural amino acids. Submitted to Biochemistry.

Datta, D.; Wang, P.; Carrico, I. S.; Mayo, S. L.; Tirrell, D. A. (2002) A designed phenylalanyl-tRNA synthetase variant allows efficient in vivo incorporation of aryl ketone functionality into proteins. J. Am. Chem. Soc. 124, 5652-5653.

Kirshenbaum, K.; Carrico, I. S.; Tirrell, D. A. (2002) Biosynthesis of proteins incorporating a versatile set of phenylalanine analogs. ChemBioChem. 3, 235-237.

Pierce, D.A.; Jotterand, N.; Carrico, I.S.; Imperiali, B. (2001) Derivatives of 8-hydroxy-2-methylquinoline are powerful prototypes for zinc sensors in biological systems. J. Am. Chem. Soc. 123, 5160-5161.

Lipshutz, B. H.; James, B.; Vance, S.; Carrico, I. S. (1997) A potentially general intramolecular biaryl coupling approach to optically pure 2,2’-BINOL analogs. Tet. Let. 38, 753-756.