Lectins are ubiquitous (glycoproteins) of plant or animal origin with excellent biological properties. Marine species are a rich source of lectins, among which those from marine sponges have received much attention for their specific biological activities, such as toxic effects on cells and pro-inflammatory activities.
As a professional biology company, CD BioGlyco has fully grasped the knowledge and technology of Marine Lectin research and provides Heliclona cratera lectin production services to clients from all kinds of industries.
The sponge Heliclona cratera samples are cut into small pieces and placed in a blender and the lectins are extracted using tris-buffered saline (TBS) as an extraction buffer. After some time, the buffer containing the lectin is filtered and the filtrate is centrifuged at high speed in a low-temperature environment. After centrifugation is completed, the supernatant is collected and lyophilized to get to Heliclona cratera lectin extract.
Heliclona cratera lectin can be adequately purified using ion exchange and gel chromatography.
The extracted crude Heliclona cratera lectin is injected into an ion exchange chromatography column and eluted with buffer. The eluate containing Heliclona cratera lectin is collected according to the signal of the protein peak in the spectrum of the ion exchange chromatography, and the preliminary purification is completed by removing the eluate.
The preliminary purified Heliclona cratera lectin is injected into a gel chromatography column and eluted using a specific eluent, the eluent containing Heliclona cratera lectin is collected, and the eluent is removed to arrive at a pure product of Heliclona cratera lectin. This step effectively removes large molecular impurities such as proteins.
We use mass spectrometry (MS) and nuclear magnetic resonance (NMR) techniques to characterize the structure of Heliclona cratera lectins, such as the order of linkages, the conformation of the sugar chains, and the glycan composition.
Of these, the primary structure of Heliclona cratera lectin is determined in part by MS/MS.
Gel permeation chromatography (GPC) is effective in detecting the natural molecular weight of Heliclona cratera lectin.
Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) can determine the relative and subunit molecular weights of Heliclona cratera lectin.
The amino acid composition of Heliclona cratera lectin is determined directly using an automated amino acid analyzer.
Saline, diluted Heliclona cratera lectin, and erythrocyte suspension are added sequentially to the wells of a well plate and the haemagglutination of Heliclona cratera lectin is observed after incubation for some time.
An aqueous solution of different glycans is added to the wells of the well plates and Heliclona cratera lectin and erythrocyte suspension are sequentially added to them, and the state of the erythrocytes is observed under a microscope after some time, to assess the inhibitory effect of glycans on Heliclona cratera lectin.
What is the definition of lectin?
Lectins are glycan-binding proteins or glycoproteins of non-immune origin and should have the ability to cause cells to agglutinate or glycoconjugate or precipitate glycoconjugates. This definition contains three key points:
What biotechnological potential exists for sponge lectins?
CD BioGlyco is a global glycobiology research company with a background and expertise in all types of glycans, lectins, and other sugar-related biomolecules. We have completed a large number of successful lectin production projects from a variety of industries and have received numerous accolades. Please feel free to
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