Journal
PEPTIDE SCIENCE
Volume 113, Issue 3, Pages -Publisher
WILEY
DOI: 10.1002/pep2.24206
Keywords
neuroendocrine regulatory peptide-2; neuropeptide; nuclear magnetic resonance; VGF
Categories
Funding
- Korea Basic Science Institute [D36401, C030440]
- National Research Foundation of Korea [2017R1A2B4012546, 2019R1A6A1A03031807, 2020M3E5E2039159]
- National Research Foundation of Korea [2020M3E5E2039159, 2017R1A2B4012546] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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NERP-2, derived from the VGF neuropeptide precursor, exhibits a partially helical structure in buffer solutions, while showing a more stable helical structure in HFIP or DPC micelle. The NMR spectroscopy determined its 3D structure in both types of solutions, showing predominantly helical structure in HFIP and partial helical structure in DPC solutions. The amphipathic nature of the helical structure suggests potential structural changes in NERP-2 upon receptor binding.
Neuroendocrine regulatory peptide-2 (NERP-2) is involved in the maintenance of homeostasis and regulates various metabolic activities. NERP-2 is derived from the VGF neuropeptide precursor, which is induced by various neurotrophins. Despite increasing interest in the functions of NERP-2, the structure of this peptide has not been reported. In this study, the structure of the NERP-2 peptide was investigated using circular dichroism and nuclear magnetic resonance (NMR) spectroscopy. NERP-2 exists as a partial helical structure in buffer solutions, and the helical structure exhibits more stable behaviors in hexafluoroisopropanol (HFIP) or dodecylphosphocholine (DPC) micelle. We determined its 3D structure in both HFIP and DPC micelle solutions using NMR spectroscopy. NERP-2 adopted a predominantly helical structure in HFIP solutions, while only the central portion of the protein was helical in the DPC solutions. The amphipathic nature of helical structure implies the potential structural changes in NERP-2 upon receptor binding.
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