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Expression of trypsin-like serine peptidases in pre-imaginal stages of Aedes aegypti (Diptera: Culicidae).
- Source :
-
Archives of insect biochemistry and physiology [Arch Insect Biochem Physiol] 2011 Apr; Vol. 76 (4), pp. 223-35. Date of Electronic Publication: 2011 Feb 09. - Publication Year :
- 2011
-
Abstract
- This study reports the biochemical characterization and comparative analyses of highly active serine proteases in the larval and pupal developmental stages of Aedes aegypti (Linnaeus) using substrate-SDS-PAGE. Zymographic analysis of larval stadia detected proteolytic activity in 6-8 bands with apparent molecular masses ranging from 20 to 250 kDa, with activity observed from pH 5.5 to 10.0. The pupal stage showed a complex proteolytic activity in at least 11 bands with apparent Mr ranging from 25 to 250 kDa, and pH optimum at 10.0. The proteolytic activities of both larval and pupal stages were strongly inhibited by phenyl-methyl sulfonyl-fluoride and N-α-Tosyl-L-lysine chloromethyl ketone hydrochloride, indicating that the main proteases expressed by these developmental stages are trypsin-like serine proteases. The enzymes were active at temperatures ranging from 4 to 85°C, with optimal activity between 37 and 60°C, and low activity at 85°C. Comparative analysis between the proteolytic enzymes expressed by larvae and pupae showed that substantial changes in the expression of active trypsin-like serine proteases occur during the developmental cycle of A. aegypti.<br /> (© 2011 Wiley-Liss, Inc.)
- Subjects :
- Aedes metabolism
Animals
Larva enzymology
Larva metabolism
Molecular Weight
Pepstatins pharmacology
Phenanthrolines pharmacology
Phenylmethylsulfonyl Fluoride pharmacology
Protease Inhibitors pharmacology
Pupa enzymology
Pupa metabolism
Serine Endopeptidases isolation & purification
Serine Endopeptidases metabolism
Tosyllysine Chloromethyl Ketone pharmacology
Tosylphenylalanyl Chloromethyl Ketone pharmacology
Aedes enzymology
Serine Endopeptidases biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1520-6327
- Volume :
- 76
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Archives of insect biochemistry and physiology
- Publication Type :
- Academic Journal
- Accession number :
- 21308760
- Full Text :
- https://doi.org/10.1002/arch.20412