1. Post-translational modifications of the insect sulfakinins. Sulfation, pyroglutamate-formation and O-methylation of glutamic acid
- Author
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Jürgen Rapus, Roland Kellner, Reinhard Predel, Ronald J. Nachman, Wolf F. Brandt, and Gerd Gäde
- Subjects
Male ,Time Factors ,Molecular Sequence Data ,Glutamic Acid ,Cockroaches ,Peptide ,Biology ,Methylation ,Biochemistry ,Mass Spectrometry ,chemistry.chemical_compound ,Sulfation ,Peptide synthesis ,Animals ,Amino Acid Sequence ,Chromatography, High Pressure Liquid ,chemistry.chemical_classification ,Edman degradation ,Neuropeptides ,Hindgut ,Glutamic acid ,biology.organism_classification ,Pyrrolidonecarboxylic Acid ,chemistry ,Insect Proteins ,American cockroach ,Corpus allatum ,Protein Processing, Post-Translational - Abstract
We identified and chemically characterized the two major forms of sulfakinins from an extract of 800 corpora cardiaca/corpora allata complexes of the American cockroach, Periplaneta americana. Bioactivity during the purification was monitored by measuring heart beat frequency in a preparation in situ. By Edman degradation analysis and MS, these main forms were identified as having the primary structures Pea-SK [EQFDDY(SO(3)H)GHMRFamide] and Lem-SK-2 [pQSDDY(SO(3)H)GHMRFamide]. The sulfation was confirmed by UV, MS and peptide synthesis. In addition, post-translationally modified sulfakinins of both major forms were isolated and identified. Firstly, nonsulfated forms of these peptides are present in considerable amounts in the corpora cardiaca/allata. Secondly, the N-terminally blocked Pea-SK and the nonblocked Lem-SK-2 occur naturally in neurohaemal release sites. Thirdly, modified Pea-SK with O-methylated glutamic acid occurs which is not an artefact of peptide purification. The major forms of the sulfakinins were shown to be highly active on both the heart and hindgut with threshold concentrations of approximately 5 x 10(-10) M (heart) and 2 x 10(-9) M (hindgut).
- Published
- 1999
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