33 results about "Glycoproteomics" patented technology

Methods for producing isotopically-labelled peptides are provided. Aspects of the method include: contacting a sample including a metabolically tagged protein with a cleavable probe to produce a probe-protein conjugate; separating the probe-protein conjugate from the sample; digesting the probe-protein conjugate to produce a probe-peptide conjugate; and cleaving a cleavable linker to release an isotopically labelled peptide. The method may further include: identifying a predetermined isotopic pattern in a mass spectrum; determining an amino acid sequence of the isotopically labelled peptide; and identifying the site of protein glycosylation based on the determined amino acid sequence. Also provided are cleavable probes for practicing the subject methods, described by the Formula: A-L-(M-Z) where A is an affinity tag, L is a cleavable linker, M is an isotopic label and Z is a chemoselective tag capable of cross-linking a metabolically tagged protein. Compositions and kits for practicing the subject methods are also provided.

The invention relates to a polymer chain-modified silica gel matrix hydrophilic interaction chromatographic stationary phase and a preparation method and application thereof. Using silica gel particles as the substrate, graft hydroxyl-containing ethylenic monomers and methylenebisacrylamide on the surface of silica gel through the click copolymerization reaction of thiol-ene to form a surface with three-dimensional dendritic polymer chains rich in hydroxyl and amide affinity. Hydrophilic interaction chromatography stationary phase with aqueous functional groups. The introduction of hydrophilic functional groups such as hydroxyl and amides according to the method of the present invention not only overcomes the shortcomings of traditional post-modification methods, such as tedious steps and low reaction efficiency, but also the three-dimensional polymer chain structure on the surface can form a rich hydrophilic layer , has a better advantage as a hydrophilic chromatography stationary phase. The liquid chromatography stationary phase provided by the invention has a novel structure and excellent hydrophilicity, and can be widely used in the separation of various samples and the selective enrichment and separation of glycopeptides, and has great potential in the fields of separation analysis and glycoproteomics. Strong practical value.

The invention relates to preparation of chitosan hydrophilic macroporous monolithic material by freeze-drying method and application thereof. The specific preparation process uses chitosan as a monomer, polyethylene glycol diglycidyl ether as a crosslinking agent, and acetic acid solution as a solvent to prepare the chitosan hydrophilic monolithic material by freeze-drying. The overall material of the present invention is low in cost, green and environmentally friendly, has good specific adsorption effect on glycopeptides in complex samples, and has strong application potential in glycoproteomics research.

The invention discloses a lectin simulant preparation method based on a molecular imprinting technique. The preparation method includes the steps: firstly, acquiring a carbohydrate chain on complete glycoprotein as a template molecule by enzyme digestion reaction; secondly, fixing the template molecule on the surface of a boric acid functional substrate material by the aid of a boric affinity function; thirdly, performing condensation reaction by the aid of silanization reagents to form an imprinting layer; finally, removing a template under the acid conditions to form an imprinting cavity to obtain a lectin simulant based on molecular imprinting. The lectin simulant is simple to prepare, low in cost, stable in nature, excellent in specificity and affinity and high in anti-jamming capacity, a recognized target object is more easily released, integrated glycoprotein can be recognized, characteristic fragments such as glycopeptides and glycan of the glycoprotein can be recognized, and the lectin simulant still can keep single-minded recognized capacity in used for complex biological samples and has an excellent application prospect in aspects such as glycoproteomics, metabonomics, glycobiology, disease diagnosis and analeptic inspection.