TY - JOUR
T1 - Screening for post-translational modifications in conotoxins using liquid chromatography/mass spectrometry
T2 - an important component of conotoxin discovery
AU - Jakubowski, Jennifer A.
AU - Kelley, Wayne P.
AU - Sweedler, Jonathan V
N1 - Funding Information:
We gratefully acknowledge several researchers as follows for numerous fascinating discussions on Conus peptides as well as for collecting animals and supplying venom samples to us: Don Barclay, Jon-Paul Bingham, Ken R. Gayler, William F. Gilly, David A. Keays, Bruce G. Livett, Alex P. Norton, David W. Sandall and Joseph R. Schulz. This research was supported by the National Institutes of Health (Grant NS31609 to J.V.S.).
PY - 2006/5
Y1 - 2006/5
N2 - Mass spectrometry has emerged as an important technique for conotoxin analysis due to its capacity for selective, sensitive, information-rich analyses. Using liquid chromatography/mass spectrometry, Conus venom can be fractionated and the peptides surveyed for specific post-translational modifications, indicating those toxin components likely to have an important biological function. With Conus striatus and Conus victoriae venom as models, bromination, carboxylation and glycosylation modifications are identified through characteristics such as isotopic distribution and labile losses observed during mass spectrometric analysis. This modification screening approach enables the identification of a C. victoriae bromo-carboxy-conotoxin, designated vc5c, as a candidate for detailed mass spectrometric analysis. Using a cDNA sequence coupled with liquid chromatography/mass spectrometry and nanoelectrospray ionization-ion trap-mass spectrometry, the sequence of vc5c is determined to be ICCYPNXWCCD, where W is 6-bromotryptophan, X is γ-carboxy glutamate and C is disulfide-linked cysteine. This represents the ninth T-superfamily (-CC-CC- scaffold) toxin that has been isolated from venom and characterized.
AB - Mass spectrometry has emerged as an important technique for conotoxin analysis due to its capacity for selective, sensitive, information-rich analyses. Using liquid chromatography/mass spectrometry, Conus venom can be fractionated and the peptides surveyed for specific post-translational modifications, indicating those toxin components likely to have an important biological function. With Conus striatus and Conus victoriae venom as models, bromination, carboxylation and glycosylation modifications are identified through characteristics such as isotopic distribution and labile losses observed during mass spectrometric analysis. This modification screening approach enables the identification of a C. victoriae bromo-carboxy-conotoxin, designated vc5c, as a candidate for detailed mass spectrometric analysis. Using a cDNA sequence coupled with liquid chromatography/mass spectrometry and nanoelectrospray ionization-ion trap-mass spectrometry, the sequence of vc5c is determined to be ICCYPNXWCCD, where W is 6-bromotryptophan, X is γ-carboxy glutamate and C is disulfide-linked cysteine. This represents the ninth T-superfamily (-CC-CC- scaffold) toxin that has been isolated from venom and characterized.
KW - Conopeptide
KW - Conus striatus
KW - Conus victoriae
KW - Electrospray ionization-mass spectrometry
KW - Toxin
KW - Venom
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U2 - 10.1016/j.toxicon.2006.01.021
DO - 10.1016/j.toxicon.2006.01.021
M3 - Article
C2 - 16574181
AN - SCOPUS:33646134111
SN - 0041-0101
VL - 47
SP - 688
EP - 699
JO - Toxicon
JF - Toxicon
IS - 6
ER -