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Glycans are involved in many fundamental cellular processes such as growth, differentiation, and morphogenesis. However, their broad structural diversity makes analysis difficult. Glycomics via mass spectrometry has focused on the composition of glycans, but informatics analysis has not kept pace with the development of instrumentation and measurement techniques. We developed Toolbox Accelerating Glycomics (TAG), in which glycans can be added manually to the glycan list that can be freely designed with labels and sialic acid modifications, and fast processing is possible. In the present work, we improved TAG for large-scale analysis such as cohort analysis of serum samples. The sialic acid linkage-specific alkylamidation (SALSA) method converts differences in linkages such as α2,3- and α2,6-linkages of sialic acids into differences in mass. Glycans modified by SALSA and several structures discovered in recent years were added to the glycan list. A routine to generate calibration curves has been implemented to explore quantitation. These improvements are based on redefinitions of residues and glycans in the TAG List to incorporate information on glycans that could not be attributed because it was not assumed in the previous version of TAG. These functions were verified through analysis of purchased sera and 74 spectra with linearity at the level of R2 > 0.8 with 81 estimated glycan structures obtained including some candidate of rare glycans such as those with the N,N’-diacetyllactosediamine structure, suggesting they can be applied to large-scale analyses.
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http://dx.doi.org/10.3390/ijms232113097 | DOI Listing |
Med Phys
September 2025
Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Background: In clinical radiation therapy (RT), accurately quantifying the delivered radiation dose to the targeted tumors and surrounding tissues is essential for evaluating treatment outcomes. Ionizing radiation acoustic imaging (iRAI), a novel passive and non-invasive imaging technique, has the potential to provide real-time in vivo radiation dose mapping during RT. However, current iRAI technology does not account for spatial variations in the detection sensitivity of the ultrasound transducer used to capture the iRAI signals, leading to significant errors in dose mapping.
View Article and Find Full Text PDFTalanta
August 2025
National Institutes for Food and Drug Control, Beijing, 102629, P.R. China; State Key Laboratory of Drug Regulatory Science, Beijing, 102629, P.R. China. Electronic address:
As concealment methods for illegal cosmetic adulteration advance, identifying non-library or unexpected additives remains challenging. This study presents a novel integrated strategy for rapid, non-targeted detection of reference-standard-free illegal cosmetic additives, especially emerging structural analogs of known prohibited compounds. The quinolone case study validated the strategy's broad applicability to cosmetics.
View Article and Find Full Text PDFHGG Adv
August 2025
Pediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD 57104, USA; Sanford School of Medicine, University of South Dakota, Sioux Falls, SD 57105, USA. Electronic address:
The increasing availability and affordability of genetic testing has resulted in the identification of numerous novel variants associated with neurodevelopmental disorders. There remains a need for methods to analyze the functional impact of these variants. Some methods, like expressing these variants in cell culture, may be rapid, but they lack physiologic context.
View Article and Find Full Text PDFMetab Eng
August 2025
Microbial Biotechnology, Campus Straubing for Biotechnology and Sustainability, Technical University of Munich, 94315, Straubing, Germany; Munich Institute of Integrated Materials, Energy and Process Engineering, Technical University of Munich, 85748, Garching, Germany; SynBiofoundry@TUM, Technical
The exploitation of Vibrio natriegens as an unconventional host for biotechnology has progressed rapidly. This development is not only a result of the remarkable high growth rate of this marine bacterium on different substrates but is also possible due to good handling properties, a versatile metabolism and its inherent natural competence - features that have facilitated the development of a sophisticated genetic engineering and synthetic biology toolbox. The availability of robust metabolic and regulatory data enables a model-based quantitative description of metabolic routes and accelerates rational metabolic engineering of the facultative anaerobic bacterium.
View Article and Find Full Text PDFMicrobiol Mol Biol Rev
August 2025
Flinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Adelaide, South Australia, Australia.
SUMMARYUnderstanding protein functions is crucial for interpreting microbial life; however, reliable function annotation remains a major challenge in computational biology. Despite significant advances in bioinformatics methods, ~30% of all bacterial and ~65% of all bacteriophage (phage) protein sequences cannot be confidently annotated. In this review, we examine state-of-the-art bioinformatics tools and methodologies for annotating bacterial and phage proteins, particularly those of unknown or poorly characterized function.
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