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Isolation and characterization of NGFFYamide neuropeptide from Patiria pectinifera pyloric caeca extract.
Kubarova, Anastasia; Go, Hye-Jin; Oh, Hye Young; Park, Soohyun; Oh, Hyun-Myoung; Park, Nam Gyu.
Afiliación
  • Kubarova A; Institute of Marine Life Science, Pukyong National University, Busan 48513, Republic of Korea.
  • Go HJ; Institute of Marine Living Modified Organisms, Pukyong National University, Busan 48513, Republic of Korea.
  • Oh HY; Institute of Marine Life Science, Pukyong National University, Busan 48513, Republic of Korea.
  • Park S; School of Marine and Fisheries Life Science (Major in Biotechnology), Pukyong National University, Busan 48513, Republic of Korea.
  • Oh HM; Institute of Liberal Arts Education, Pukyong National University, Busan 48547, Republic of Korea.
  • Park NG; Institute of Marine Life Science, Pukyong National University, Busan 48513, Republic of Korea; Department of Biotechnology, College of Fisheries Sciences, Pukyong National University, Busan 48513, Republic of Korea. Electronic address: ngpark@pknu.ac.kr.
Peptides ; 180: 171282, 2024 Oct.
Article en En | MEDLINE | ID: mdl-39134260
ABSTRACT
Neuropeptides are small molecules that mediate intercellular signaling and regulate physiological processes. Starfish possess various myoactive neuropeptides, including starfish myorelaxant peptide (SMP) and a calcitonin-type peptide with apical muscle relaxing properties. In this study, we report the purification of a neuropeptide from starfish (Patiria pectinifera) pyloric caeca extract using high-performance liquid chromatography (HPLC) and an in vitro bioassay to screen for fractions and peptides with relaxing effects on P. pectinifera apical muscle preparations. A series of HPLC steps using reversed-phase and cation-exchange columns yielded a purified peptide with muscle-relaxing effects. The purified peptide's structure was determined by LC-MS and Edman degradation, revealing a pentapeptide with an amidated C-terminus (NGFFYamide) and a molecular mass of 646.2930 Da. This is the first report of NGFFYamide purification from P. pectinifera through biochemical methods. The nucleotide sequence encoding the NGFFYamide precursor was determined, showing the presence of a conserved neurophysin domain in the C-terminal region. RT-qPCR results confirmed high expression in radial nerves cord, consistent with previous findings on NG peptides in echinoderms. In vitro pharmacological studies on muscle preparations from P. pectinifera and Asterias amurensis revealed differential relaxing activity of NGFFYamide on apical muscles, while its effects on tube foot preparations were similar in both species. NGFFYamide also induced potent contraction in P. pectinifera cardiac stomach. Comparison of three NG peptides (NGFFYamide, NGFFFamide, and NGIWYamide) on P. pectinifera cardiac stomach revealed varying potency, suggesting class-specific receptor interactions. Tachyphylaxis was observed in P. pectinifera apical muscle but not in A. amurensis, warranting further investigation. Based on these results, it is plausible that NGFFYamide could be involved in regulating locomotion and feeding behavior in P. pectinifera, consistent with findings in Asterias rubens.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Estrellas de Mar / Neuropéptidos Idioma: En Revista: Peptides Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Estrellas de Mar / Neuropéptidos Idioma: En Revista: Peptides Año: 2024 Tipo del documento: Article