Lack of signal peptide in insect prophenoloxidase to avoid glycosylation to damage the zymogen activity
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
39029607
DOI
10.1016/j.dci.2024.105230
PII: S0145-305X(24)00102-2
Knihovny.cz E-resources
- Keywords
- Enzyme activity, Glycosylation, Insect, Prophenoloxidase, Signal peptide,
- MeSH
- Cell Line MeSH
- Drosophila melanogaster * immunology metabolism MeSH
- Glycosylation MeSH
- Insect Proteins metabolism genetics MeSH
- Catechol Oxidase * metabolism MeSH
- Larva metabolism MeSH
- Humans MeSH
- Enzyme Precursors * metabolism MeSH
- Protein Precursors metabolism MeSH
- Protein Sorting Signals * MeSH
- Drosophila Proteins metabolism genetics MeSH
- Monophenol Monooxygenase metabolism MeSH
- Calcium metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Insect Proteins MeSH
- Catechol Oxidase * MeSH
- Enzyme Precursors * MeSH
- pro-phenoloxidase MeSH Browser
- Protein Precursors MeSH
- Protein Sorting Signals * MeSH
- Drosophila Proteins MeSH
- Monophenol Monooxygenase MeSH
- Calcium MeSH
Insect prophenoloxidases (PPOs) are important immunity proteins for defending against the invading pathogens and parasites. As a Type-Ⅲ copper-containing proteins, unlike Homo sapiens tyrosinases, the insect PPOs and most bacterial tyrosinases contain no signal peptides for unknown reason, however they can still be released. To this end, we fused different signal peptides to Drosophila melanogaster PPOs for in vitro and in vivo expression, respectively. We demonstrate that an artificial signal peptide can help PPO secretion in vitro. The secreted PPO appeared larger than wild-type PPO on molecular weight sizes due to glycosylation when expressed in S2 cells. Two asparagine residues for potential glycosylation in PPO1 were identified when a signal peptide was fused. After purification, the glycosylated PPO1 lost zymogen activity. When PPO1 containing a signal peptide was over-expressed in Drosophila larvae, the glycosylation and secretion of PPO1 was detected in vivo. Unlike insect PPO, human tyrosinase needs a signal peptide for protein expression and maintaining enzyme activity. An artificial signal peptide fused to bacterial tyrosinase had no influence on the protein expression and enzyme activity. These Type-Ⅲ copper-containing proteins from different organisms may evolve to perform their specific functions. Intriguingly, our study revealed that the addition of calcium inhibits PPO secretion from the transiently cultured larval hindguts in vitro, indicating that the calcium concentration may regulate PPO secretion. Taken together, insect PPOs can maintain enzyme activities without any signal peptide.
College of Life Sciences Shangrao Normal University Shangrao 334001 China
Institute of Entomology Biology Centre CAS Branisovska 31 370 05 Ceske Budejovice Czech Republic
Life Science Institute Jinzhou Medical University Jinzhou 121001 China
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