Sponge extracts can agglutinate erythrocytes and have a specific agglutinating effect on human erythrocytes. Therefore, in-depth research on Sponge-derived Lectin is a topic of great biological importance. As a result of research, it has been shown that lectin from the marine sponge Cliona varians is a tetrameric glycoprotein, linked by disulfide bonds, which has a good physiological defense effect.
With superior Marine Biomolecule Production skills, CD BioGlyco has won a lot of accolades in the field of Marine Lectin Production. Here, we provide professional Cliona varians lectin production service to our clients.
After clipping the sponge Cliona varians, a buffer solution is used to extract lectin directly. The pH of the buffer is usually between 7-8, which will produce an osmotic shock to the Cliona varians cells, thus disrupting the cell membrane and extracting the lectin molecules.
To enrich lectins, we offer precipitation methods. Among other things, Ca2+ precipitation helps to promote the enrichment of lectins that are structurally dependent on Ca2+. Acetone precipitation is also an effective method for concentrating proteins in extracts.
Purification of Cliona varians lectin is mainly carried out by chromatography. Here, we offer a variety of methods for purifying Cliona varians lectin for clients to choose from.
Gel electrophoresis and gel permeation chromatography (GPC) can be used to detect the multilevel structure of Cliona varians lectin.
Mass spectrometry (MS) can be used to detect the subunit structure of Cliona varians lectin.
We utilize sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and GPC to determine the subunit molecular weight and overall relative molecular mass of the subunit of Cliona varians lectin.
Diluted Cliona varians lectin and erythrocyte suspension are gradually added to the microtiter plate and incubated at room temperature for a while, and then the haemagglutinating activity of lectin is observed under the microscope.
Technology: SDS-PAGE and size exclusion chromatography (SEC)
Journal: Anais da Academia Brasileira de Ciências
IF: 2.3
Published: 2015
Results: In this article, the authors extracted Cliona varians lectin CvL-1 and CvL-2 using acetone precipitation, purified them by SEC, detected the molecular weights of CvL-1 and CvL-2 by SDS-PAGE and SEC, and also screened for haemagglutination activity. The results showed that CvL-2 is a trimeric protein with a subunit of 175 kDa. it was able to agglutinate rabbit erythrocytes and was inhibited by galactosides. In addition, CvL-2 showed toxicity to Artemia naplii and the LC 50 of CvL-2 was 850.1 μg/mL.
Fig.1 Size exclusion chromatograms of CvL-1 and CvL-2. (Moura, et al., 2015)
What types of sponge lectins exist?
Classified according to the primary structure of the lectin, sponge lectins can be divided into galactose lectins, C-type lectins, tachykinin-like lectins, and F-type lectins.
What is the physiological role of sponge lectins?
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