Retrograde labeling of single neurons in conjunction with MALDI high-energy collision-induced dissociation MS/MS analysis for peptide profiling and structural characterization

Anal Chem. 2003 Jul 1;75(13):2996-3000. doi: 10.1021/ac034057q.

Abstract

To reveal the peptide contents of the visually nonidentifiable neurons from a neuronal circuit of interest, we combined retrograde labeling of neurons with mass spectrometric single cell analysis. We used the neuronal circuit involved in the copulation behavior of a freshwater snail, Lymnaea stagnalis, as a model. Central neurons that control this behavior are known to send their axons to the penis nerve and innervate the penis complex. By retrograde filling from the penis nerve with nickel-lysine, these neurons were selectively labeled darkish blue. Matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometric analyses of single stained neurons in the parietal ganglion from different animals reveal consistently the presence of several molecular ion species in the range of 800-1200 Da. From a single neuron, six molecular ion species were further characterized with MALDI time-of-flight/time-of-flight mass spectrometry, which demonstrates that the peptides are derived from a previously reported -FLRFamide precursor.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Lymnaea / chemistry
  • Lymnaea / cytology
  • Male
  • Molecular Sequence Data
  • Neurons / chemistry*
  • Neuropeptides / analysis*
  • Neuropeptides / chemistry*
  • Penis / cytology
  • Penis / innervation
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization / methods
  • Staining and Labeling / methods

Substances

  • Neuropeptides