Characterization of a C-type lectin from the cotton bollworm, Helicoverpa armigera
Developmental & Comparative Immunology, ISSN: 0145-305X, Vol: 33, Issue: 6, Page: 772-779
2009
- 51Citations
- 38Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations51
- Citation Indexes51
- 51
- CrossRef40
- Captures38
- Readers38
- 38
Article Description
C-type lectins can specifically recognize sugars on the surface of microorganisms and cause a series of immune responses to effectively resist pathogenic invasions. In previous work in our laboratory, we obtained a C-type lectin from Helicoverpa armigera (Ha-lectin). It has two different carbohydrate recognition domains (CRDs) CRD1 and CRD2 arranged in tandem. In this study, recombinant CRD1 and CRD2 were expressed separately in Escherichia coli and purified. They have the ability to agglutinate Gram-negative and Gram-positive bacteria and fungi in the presence of Ca 2+. They also have different spectra of sugar binding abilities. The rHa-lectin, rCRD1 and rCRD2 could inhibit the growth in quantity of Bacillus thuringiensis in vivo by increasing hemocyte phagocytosis. These results suggested that Ha-lectin and its two domains could function as a pattern recognition receptor or an opsonin in vivo to promote the hemocyte phagocytosis of pathogens and protect the insect from bacterial infection.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0145305X09000160; http://dx.doi.org/10.1016/j.dci.2009.01.002; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=60849132999&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/19185587; https://linkinghub.elsevier.com/retrieve/pii/S0145305X09000160; https://dx.doi.org/10.1016/j.dci.2009.01.002
Elsevier BV
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