Abstract
A strategy for locating multiple disulfide bridges is demonstrated using two MVIIA and MVIIC ω-conotoxins in which the locations of disulfide bridges are known. The method is based on the use of selective trypsin digestion followed by non-selective pronase digestion in combination with electrospray mass spectrometry. This strategy promises to be a suitable first step in investigations applied to new peptides of unknown structure.
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