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Identification of novel Cry1Ac binding proteins in midgut membranes from Heliothis virescens using proteomic analyses.
- Source :
-
Insect biochemistry and molecular biology [Insect Biochem Mol Biol] 2007 Mar; Vol. 37 (3), pp. 189-201. Date of Electronic Publication: 2006 Oct 28. - Publication Year :
- 2007
-
Abstract
- Proteins such as aminopeptidases and alkaline phosphatases, both glycosyl-phosphatidyl-inositol (GPI) anchored proteins, were previously identified as Cry1Ac binding proteins in the Heliothis virescens midgut. To identify additional toxin binding proteins, brush border membrane vesicles from H. virescens larvae were treated with phosphatidyl inositol phospholipase C, and released proteins were resolved by two-dimensional electrophoresis. Protein spots selected by their ability to bind Cry1Ac were identified by MALDI-TOF mass spectrometry coupled to peptide mass fingerprinting (PMF) and database searching. As in previous studies, H. virescens alkaline phosphatase was identified as a Cry1Ac binding protein. V-ATP synthase subunit A and actin were identified as novel Cry1Ac binding proteins in H. virescens. Additional toxin-binding proteins were predicted based on MS/MS fragmentation and de novo sequencing, providing amino acid sequences that were used in database searches to identify a phosphatase and a putative protein of the cadherin superfamily as additional Cry1Ac binding proteins.
- Subjects :
- Animals
Bacillus thuringiensis Toxins
Electrophoresis, Gel, Two-Dimensional
Gastrointestinal Tract chemistry
Gastrointestinal Tract cytology
Glycosylphosphatidylinositols metabolism
Mass Spectrometry
Peptide Mapping
Bacterial Proteins metabolism
Bacterial Toxins metabolism
Endotoxins metabolism
Hemolysin Proteins metabolism
Insect Proteins chemistry
Microvilli chemistry
Moths chemistry
Proteomics
Receptors, Cell Surface chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0965-1748
- Volume :
- 37
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Insect biochemistry and molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 17296494
- Full Text :
- https://doi.org/10.1016/j.ibmb.2006.10.004