4.7 Article

Mass spectrometry profiling and quantitation of changes in circulating hormones secreted over time in Cancer borealis hemolymph due to feeding behavior

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 414, Issue 1, Pages 533-543

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03479-1

Keywords

Crustacean; Neuropeptides; Data-independent acquisition mass spectrometry (DIA MS); Peptidomics; Peptide hormone; Hemolymph

Funding

  1. National Science Foundation [CHE-1710140]
  2. National Institutes of Health [R01DK071801, R01NS029436]
  3. National Institutes of Health, under Ruth L. Kirschstein National Research Service Award from the National Heart Lung and Blood Institute [T32 HL 007936]
  4. National Institutes of Health-General Medical Sciences F31 National Research Service Award [1F31GM126870-01A1]
  5. NIH [S10RR029531]
  6. Office of the Vice Chancellor for Research and Graduate Education at the University of Wisconsin-Madison
  7. Wisconsin Alumni Research Foundation
  8. University of WisconsinMadison School of Pharmacy

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The study utilized DIA mass spectrometry to improve the detection of neuropeptides in the crustacean stomatogastric ganglion, revealing differences in the presence and relative abundance of neuropeptides at different stages of the feeding process. Additionally, 96 putative neuropeptide sequences were identified through de novo sequencing, indicating the potential existence of more key modulators within this system.
The crustacean stomatogastric ganglion (STG) is a valuable model for understanding circuit dynamics in neuroscience as it contains a small number of neurons, all easily distinguishable and most of which contribute to two complementary feeding-related neural circuits. These circuits are modulated by numerous neuropeptides, with many gaining access to the STG as hemolymph-transported hormones. Previous work characterized neuropeptides in the hemolymph of the crab Cancer borealis but was limited by low peptide abundance in the presence of a complex biological matrix and the propensity for rapid peptide degradation. To improve their detection, a data-independent acquisition (DIA) mass spectrometry (MS) method was implemented. This approach improved the number of neuropeptides detected by approximately twofold and showed greater reproducibility between experimental and biological replicates. This method was then used to profile neuropeptides at different stages of the feeding process, including hemolymph from crabs that were unfed, or 0 min, 15 min, 1 h, and 2 h post-feeding. The results show differences both in the presence and relative abundance of neuropeptides at the various time points. Additionally, 96 putative neuropeptide sequences were identified with de novo sequencing, indicating there may be more key modulators within this system than is currently known. These results suggest that a distinct cohort of neuropeptides provides modulation to the STG at different times in the feeding process, providing groundwork for targeted follow-up electrophysiological studies to better understand the functional role of circulating hormones in the neural basis of feeding behavior.

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