Kulej et al., 2015 - Google Patents
Characterization of histone post-translational modifications during virus infection using mass spectrometry-based proteomicsKulej et al., 2015
View PDF- Document ID
- 9838358991808492216
- Author
- Kulej K
- Avgousti D
- Weitzman M
- Garcia B
- Publication year
- Publication venue
- Methods
External Links
Snippet
Viruses are obligate intracellular parasites that necessarily rely on hijacking cellular resources to produce viral progeny. The success of viral infection requires manipulation of host chromatin in order to activate genes useful for production of viral proteins as well as to …
- 230000004481 post-translational protein modification 0 title abstract description 60
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
- G01N33/6848—Methods of protein analysis involving mass spectrometry
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
- G01N33/6842—Proteomic analysis of subsets of protein mixtures with reduced complexity, e.g. membrane proteins, phosphoproteins, organelle proteins
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/14—Extraction; Separation; Purification
- C07K1/16—Extraction; Separation; Purification by chromatography
- C07K1/22—Affinity chromatography or related techniques based upon selective absorption processes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Kulej et al. | Characterization of histone post-translational modifications during virus infection using mass spectrometry-based proteomics | |
| Lin et al. | Examining histone posttranslational modification patterns by high-resolution mass spectrometry | |
| Ostasiewicz et al. | Proteome, phosphoproteome, and N-glycoproteome are quantitatively preserved in formalin-fixed paraffin-embedded tissue and analyzable by high-resolution mass spectrometry | |
| Kean et al. | Mass spectrometry approaches to study mammalian kinase and phosphatase associated proteins | |
| JP5763545B2 (en) | Parallel extraction of various biomolecules from formalin-fixed tissue | |
| JP2010133971A (en) | Method of proteome analysis for phosphorylated protein | |
| WO2013148178A1 (en) | Quantification of post-translational modifications on histone proteins with mass spectrometry | |
| Adelmant et al. | Tandem affinity purification and mass spectrometry (TAP‐MS) for the analysis of protein complexes | |
| CN108059649A (en) | Protein groups genomic analysis system and method | |
| JP2009156587A (en) | Analyzing method of sugar chain of glycoprotein | |
| WO2017166897A1 (en) | Proteomic reactor, protein chromatographic separation platform and use thereof | |
| Villar‐Garea et al. | Analysis of histone modifications by mass spectrometry | |
| King et al. | Enhanced sample multiplexing of tissues using combined precursor isotopic labeling and isobaric tagging (cPILOT) | |
| US20020155614A1 (en) | Peptide esterification | |
| Geshkovski et al. | Quantitative profiling of histone variants and posttranslational modifications by tandem mass spectrometry in arabidopsis | |
| Hao et al. | Proteomic analysis of protein deamidation | |
| JP7805290B2 (en) | Peptide purification formulations and methods | |
| CN103512997A (en) | Two-dimensional short-gradient high-efficiency protein component separation and identification method | |
| Lazarev et al. | Centrifugal methods and devices for rapid in‐gel digestion of proteins | |
| Iliuk | Identification of phosphorylated proteins on a global scale | |
| CN114441697B (en) | A kind of method and application of high-efficiency removal of polypeptide residues in liquid chromatography | |
| CN118076622A (en) | Method for processing and analyzing viral capsid proteins | |
| JP2023500790A (en) | Peptide purification formulations and methods | |
| US20250282833A1 (en) | Methods for processing and analyzing virus capsid proteins | |
| Lu et al. | Epurisp: combining enzymatic digestion, ultrafiltration, and rapid in situ sample purification for high-performance proteomics |