8 results about "Proteomics methods" patented technology

Discussed herein are novel engineered polypeptides which are effective at cutting and tagging H3 histone tails from endogenous histones, facilitating multiplex "cut-and-paste" middle down proteomics with tandem mass tags. This cut-and-paste proteomics approach permits the quantitative analysis of H3 histone modification crosstalk after treatment with different histone deacetylase inhibitors.

The application relates to a high-throughput identification method of lncRNA coding peptides and application thereof, and belongs to the technical field of biology. The method combines a translationomics technology and a protein mass spectrometry technology, takes ribosome footprint sequencing data as a starting point, determines an open reading frame located on an lncRNA gene according to a three-base periodicity rule of a sequencing fragment, further constructs a proteogenomics index after systematic filtration, uses a computational proteomics method to detect an lncRNA translation event, and systematically identifies lncRNA coding peptides on the basis. The method has the characteristics of modularity and strong expandability, can be widely used for various types of proteome data, and can high-throughput identify and quantitatively detect lncRNA coding peptides. The application provides a prediction of molecular typing and prognosis of cancer patients based on an lncRNA coding peptide network model, and provides an important reference basis for precise medication of clinical patients.

The invention discloses a construction method and application of an animal model with delayed embryonic development, and relates to the technical field of animal models.The construction method of the animal model with delayed embryonic development comprises the following steps that S1, an early embryo is obtained; s2, performing contact culture on the early embryo and a development retardation inducer; s3, culturing to obtain a slowly developed embryo; the proteomics analysis method based on non-data-dependent acquisition is used for analyzing an animal model with slow embryonic development. The method comprises the following steps: providing an embryo sample; obtaining a protein expression profile by adopting a non-data-dependent acquisition proteomics method; according to a protein expression profile, identifying differential expression proteins related to the embryonic development retardation; the animal model with the delayed embryonic development is constructed, and an experimental model is provided for researching a molecular mechanism of the delayed embryonic development; a non-data-dependent collection proteomics analysis method is applied to the animal model, and compared with a traditional data-dependent collection method, the method has higher stability.

The application provides a plasma exosome marker and application for early diagnosis of pancreatic cancer, utilizes a metabolomics and proteomics method, analyzes metabolites and proteins with significant differences in exosomes separated from plasma of pancreatic cancer patients, pancreatitis patients and normal persons, screens a series of biomarkers capable of early indicating a pancreatic cancer occurrence risk, and further screens a group of biomarkers to construct a pancreatic cancer diagnosis model, so that the pancreatic cancer diagnosis model can be used for conveniently and efficiently predicting whether an individual is suffering from pancreatic cancer, and meets clinical requirements.

The application discloses a pigment and a construction method of an engineering bacterium for producing the pigment. A high-expression protein is identified in a blue jellyfish umbrella epidermis through a proteomics method. It is found through sequence alignment and domain analysis that the protein is similar to a lung-shaped root mouth jellyfish blue pigment protein precursor, has a curled cysteine-rich domain and a ring cake domain, and conforms to the properties of a root mouth jellyfish order specific pigment family. Therefore, the protein is named as a jellyfish blue pigment. A jellyfish blue pigment gene expression vector is constructed, and a round red blastoconidium yeast is reformed through a genetic engineering method to construct an industrial yeast strain for producing the blue pigment. The blue pigment synthesized by the constructed strain is non-toxic and has no side effects, and can be applied to the printing and dyeing industry in the future.

This application relates to the field of chemical proteomics, and particularly to a quantitative chemical proteomics method for thiocylation modification sites. It employs aldehyde and alkyne-containing probes to chemically selectively label the proteome of biological samples with thiocylation modification. Quantitative chemical proteomics techniques are then used to quantitatively analyze the chemically labeled thiocylation modification sites. This method enables the identification and quantification of all thiocylation modification sites in biological samples, providing an analytical tool for studying the effects of thiocylation modification on protein structure and function. It facilitates research into the molecular mechanisms of thiocylation modification in related diseases, achieving high coverage, high reproducibility, and high accuracy in target screening, and providing corresponding technical support for subsequent drug development.

The invention discloses an application of TPD52 as a myasthenia gravis urine diagnostic marker, which detects and finds the difference condition of urine proteins between myasthenia gravis and a healthy control group through a high-throughput proteomics method. The TPD52 protein in the urine can be used for detecting the myasthenia gravis and healthy people, further screening is carried out, and clinical samples verify that the TPD52 protein in the urine can be used for remarkably distinguishing the myasthenia gravis from the healthy people, so that the TPD52 protein can be used as a urine diagnosis marker and is used for noninvasive detection of the myasthenia gravis, and a new way is provided for clinical early diagnosis.

The invention relates to a method for proteomic analysis and a substrate prepared for the method. The substrate is prepared with immobilized antibodies using the electrospray deposition method, where a planar conductive plate is used as the substrate, onto which ions of immunoglobulin-binding protein are deposited by electrospray, then at least one antibody with affinity for the target antigen is dispensed onto the substrate with immobilized immunoglobulin-binding protein, which is anchored via a non-covalent affinity interaction with the immobilized immunoglobulin-binding protein. Subsequently, a sample containing the antigen is dispensed onto the substrate with the immobilized immunoglobulin-binding protein and bound antibody, and the prepared substrate is incubated. After incubation of the substrate, sample residues are removed, an analyte with an antigen is chemically reduced or eluted from the substrate and cleaved with trypsin, an analyte with an antigen is desalted, and the sample is analysed using a proteomic method.