Asparaginyl-Valine
                        Formula: C9H17N3O4 (231.1219)
                        
                        Chinese Name:  天冬氨酰-缬氨酸
                        BioDeep ID: BioDeep_00000026758 
                        ( View LC/MS Profile)
                        SMILES:  CC(C)C(NC(=O)C(N)CC(=N)O)C(=O)O
                    
Found 7 Sample Hits
| m/z | Adducts | Species | Organ | Scanning | Sample | |
|---|---|---|---|---|---|---|
| 196.1053 | [M+H-2H2O]+PPM:14 | 
                                    Marker Pen | NA | DESI (None) | 
                                        3ul_0.8Mpa_RAW_20241016-PAPER PNMK - MEMI_testResolution: 30μm, 315x42
                                             By writing the four English letters “PNMK” on white paper with a marker pen, and then scanning with a DESI ion source to obtain the scanning result. The signal of the chemical substances on the marker pen used appears on the channel with an m/z value of   | 
                                    
                                        
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| 196.1085 | [M+H-2H2O]+PPM:2.3 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        LNTO22_1_4 - MTBLS385Resolution: 17μm, 82x80
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| 214.1225 | [M+H-H2O]+PPM:18.2 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        LNTO22_1_4 - MTBLS385Resolution: 17μm, 82x80
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| 231.1496 | [M-H2O+NH4]+PPM:19.2 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        LNTO22_1_4 - MTBLS385Resolution: 17μm, 82x80
                                              | 
                                    
                                        
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| 249.1547 | [M+NH4]+PPM:4.1 | 
                                    Mus musculus | Liver | MALDI (CHCA) | 
                                        Salmonella_final_pos_recal - MTBLS2671Resolution: 17μm, 691x430
                                             A more complete and holistic view on host–microbe interactions is needed to understand the physiological and cellular barriers that affect the efficacy of drug treatments and allow the discovery and development of new therapeutics. Here, we developed a multimodal imaging approach combining histopathology with mass spectrometry imaging (MSI) and same section imaging mass cytometry (IMC) to study the effects of Salmonella Typhimurium infection in the liver of a mouse model using the S. Typhimurium strains SL3261 and SL1344. This approach enables correlation of tissue morphology and specific cell phenotypes with molecular images of tissue metabolism. IMC revealed a marked increase in immune cell markers and localization in immune aggregates in infected tissues. A correlative computational method (network analysis) was deployed to find metabolic features associated with infection and revealed metabolic clusters of acetyl carnitines, as well as phosphatidylcholine and phosphatidylethanolamine plasmalogen species, which could be associated with pro-inflammatory immune cell types. By developing an IMC marker for the detection of Salmonella LPS, we were further able to identify and characterize those cell types which contained S. Typhimurium.
[dataset] Nicole Strittmatter. Holistic Characterization of a Salmonella Typhimurium Infection Model Using Integrated Molecular Imaging, metabolights_dataset, V1; 2022. https://www.ebi.ac.uk/metabolights/MTBLS2671.  | 
                                    
                                        
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| 196.1087 | [M+H-2H2O]+PPM:3.3 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        TO31T - MTBLS385Resolution: 75μm, 56x54
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| 196.1089 | [M+H-2H2O]+PPM:4.4 | 
                                    Homo sapiens | esophagus | DESI () | 
                                        TO29T - MTBLS385Resolution: 75μm, 56x48
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Asparaginyl-Valine is a dipeptide composed of asparagine and valine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.
