4.7 Article

Complementary neuropeptide detection in crustacean brain by mass spectrometry imaging using formalin and alternative aqueous tissue washes

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 413, Issue 10, Pages 2665-2673

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-020-03073-x

Keywords

Mass spectrometry imaging; Neuropeptides; Formalin; MALDI

Funding

  1. National Science Foundation [CHE-1710140]
  2. National Institutes of Health (NIH) [1R01DK071801, R56 MH110215]
  3. National Heart, Lung, and Blood Institute of the NIH [T32 HL007936-20]
  4. NIH in the form of a General Medical Sciences NRSA Fellowship [1F31GM119365]
  5. University of Wisconsin Carbone Cancer Center [233-AAC9675]
  6. UWCCC Pancreatic Cancer Taskforce
  7. Wisconsin Alumni Research Foundation
  8. University of Wisconsin-Madison School of Pharmacy
  9. NIH [S10RR029531]
  10. Office of the Vice Chancellor for Research and Graduate Education at the University of Wisconsin-Madison

Ask authors/readers for more resources

Neuropeptides are low abundance signaling molecules that modulate physiological processes, and mass spectrometry imaging is increasingly useful in studying them. Proper tissue washes can increase detectable neuropeptides, and using a salt solution wash may affect neuropeptide detection.
Neuropeptides are low abundance signaling molecules that modulate almost every physiological process, and dysregulation of neuropeptides is implicated in disease pathology. Mass spectrometry (MS) imaging is becoming increasingly useful for studying neuropeptides as new sample preparation methods for improving neuropeptide detection are developed. In particular, proper tissue washes prior to MS imaging have shown to be quick and effective strategies for increasing the number of detectable neuropeptides. Treating tissues with solvents could result in either gain or loss of detection of analytes, and characterization of these wash effects is important for studies targeting sub-classes of neuropeptides. In this communication, we apply aqueous tissue washes that contain sodium phosphate salts, including 10% neutral buffered formalin (NBF), on crustacean brain tissues. Our optimized method resulted in complementary identification of neuropeptides between washed and unwashed tissues, indicating that our wash protocol may be used to increase total neuropeptide identifications. Finally, we show that identical neuropeptides were detected between tissues treated with 10% NBF and an aqueous 1% w/v sodium phosphate solution (composition of 10% NBF without formaldehyde), suggesting that utilizing a salt solution wash affects neuropeptide detection and formaldehyde does not affect neuropeptide detection when our wash protocol is performed.

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