Publications by authors named "Darula Z"

H2A.Z-nucleosomes are present in both euchromatin and heterochromatin and it has proven difficult to interpret their disparate roles in the context of their stability features. Using an in situ assay of nucleosome stability and DT40 cells expressing engineered forms of the histone variant we show that native H2A.

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  • A murine model of colorectal cancer (CRC) was created by injecting CT26 colon carcinoma cells into the spleen of BALB/c mice to study cancer spread to the liver.
  • The presence of CRC was confirmed using specific staining techniques, and changes in white blood cell populations were investigated through immunophenotyping and lectin binding assays.
  • Proteomic analysis revealed unique protein expressions in CRC-affected tissues, identifying potential biomarkers like Galectin-1 and S100A4 that are linked to poor patient outcomes, which could inform future treatment strategies for human CRC.
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Collagen cross-links created by the lysyl oxidase and lysyl hydroxylase families of enzymes are a significant contributing factor to the biomechanical strength and rigidity of tissues, which in turn influence cell signaling and ultimately cell phenotype. In the clinic, the proteolytically liberated N-terminal cross-linked peptide of collagen I (NTX) is used as a biomarker of bone and connective tissue turnover, which is altered in several disease processes. Despite the clinical utility of these collagen breakdown products, the majority of the cross-linked peptide species have not been identified in proteomic datasets.

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  • The study investigates changes in the brain's extracellular fluid (ECF) peptidome during epileptic seizures in a rat model using a drug called 4-aminopyridine (4-AP), which induces seizures.
  • Researchers utilized in vivo microdialysis combined with electrophysiology to collect and analyze brain fluid samples, identifying 2540 peptides, with 866 linked to proteins that were altered during seizures.
  • Key findings reveal that certain neuropeptides and proteins involved in synaptic regulation and astrocyte function significantly changed following seizures, highlighting the potential of ECF analysis for monitoring brain activity and damage.
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The rotifer-specific biopolymer, namely Rotimer, is a recently discovered group of the biomolecule family. Rotimer has an active role in the biofilm formation initiated by rotifers (e.g.

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  • Toxin cargo genes, which help bacteria evolve and adapt, can be transferred between species through phages and have made their way into animal genomes, leading to new adaptations.* -
  • Researchers focused on specific insect species to investigate how these toxin genes are expressed and how they contribute to the immune response against parasitoid wasps.* -
  • Findings indicate that these toxin genes, integrated into the insects' immune systems millions of years ago, play a crucial role in enhancing resistance to parasitoid wasps, highlighting the potential for rapid evolutionary changes in animals.*
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Clear cell renal carcinoma is the most frequent type of kidney cancer, with an increasing incidence rate worldwide. In this research, we used a proteotranscriptomic approach to differentiate normal and tumor tissues in clear cell renal cell carcinoma (ccRCC). Using transcriptomic data of patients with malignant and paired normal tissue samples from gene array cohorts, we identified the top genes over-expressed in ccRCC.

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  • - Declining blood flow in the brain can lead to chronic hypoperfusion, which may result in neurodegenerative disorders like vascular dementia, as it disrupts the brain's energy supply and mitochondrial functions.
  • - Researchers performed stepwise bilateral common carotid occlusions on rats to study long-term changes in mitochondrial proteins, membranes, and cerebrospinal fluid, using advanced proteomic analyses.
  • - They identified significant changes in proteins across mitochondria, membranes, and cerebrospinal fluid, primarily linked to protein turnover, indicating that hypoperfusion can alter brain protein processes that are detectable in CSF.
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Extracellular vesicle (EV) research is a rapidly developing field, mainly due to the key role of EVs in intercellular communication and pathophysiological processes. However, the heterogeneity of EVs challenges their exploration and the establishment of gold-standard methods. Here, we aimed to reveal the influence of technical changes on EV biology and the reliability of experimental data.

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  • Analyzing O-glycosylation is more complex than N-glycopeptide characterization, with multiple layers of complexity highlighted in the study.
  • The research presents a comprehensive dataset of O-glycopeptides from human samples, including individuals with bladder cancer and bladder inflammation, making it one of the largest collections analyzed.
  • The analysis indicates a significant diversity in O-glycosylation patterns and suggests improvements for existing glycopeptide analysis tools to enhance reliability in assignments.
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The dynamic balance of transcriptional and translational regulation together with degron-controlled proteolysis shapes the ever-changing cellular proteome. While a large variety of degradation signals has been characterized, our knowledge of -acting protein motifs that can in vivo stabilize otherwise short-lived proteins is very limited. We have identified and characterized a conserved 13-mer protein segment derived from the p54/Rpn10 ubiquitin receptor subunit of the 26S proteasome, which fulfills all the characteristics of a protein stabilization motif (STABILON).

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Background And Aim: Common chickweed () tea has traditionally been applied for treatment of various metabolic diseases including diabetes in folk medicine; however, experimental evidence to support this practice is lacking. Therefore, we aimed to assess the effect of tea on glucose homeostasis and cardiac performance in a rat model of diabetes.

Experimental Procedure: Hot water extract of herb were analyzed and used in this study, where diabetes was induced by fructose-enriched diet supplemented with a single injection of streptozotocin.

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Band 3 (anion exchanger 1; AE1) is the most abundant membrane protein in red blood cells, which in turn are the most abundant cells in the human body. A compelling model posits that, at high oxygen saturation, the N-terminal cytosolic domain of AE1 binds to and inhibits glycolytic enzymes, thus diverting metabolic fluxes to the pentose phosphate pathway to generate reducing equivalents. Dysfunction of this mechanism occurs during red blood cell aging or storage under blood bank conditions, suggesting a role for AE1 in the regulation of the quality of stored blood and efficacy of transfusion, a life-saving intervention for millions of recipients worldwide.

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Introduction: Placental Protein 1 (PP1), PP8, and PP22 were isolated from the placenta. Herein, we aimed to identify PP1, PP8, and PP22 proteins and their placental and trophoblastic expression patterns to reveal potential involvement in pregnancy complications.

Methods: We analyzed PP1, PP8, and PP22 proteins with LC-MS.

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Intact glycopeptide analysis is becoming more common with developments in mass spectrometry instrumentation and fragmentation approaches. In particular, collision-based fragmentation approaches such as higher energy collisional dissociation (HCD) and radical-driven fragmentation approaches such as electron transfer dissociation (ETD) provide complementary information, but bioinformatic strategies to utilize this combined information are currently lacking. In this work we adapted a software tool, MS-Filter, to search HCD peak list files for predicted Y ions based on matched EThcD results to propose additional glycopeptide assignments.

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Glycopeptides represent cross-linked structures between chemically and physically different biomolecules. Mass spectrometric analysis of O-glycopeptides may reveal the identity of the peptide, the composition of the glycan and even the connection between certain sugar units, but usually only the combination of different MS/MS techniques provides sufficient information for reliable assignment. Currently, HCD analysis followed by diagnostic sugar fragment-triggered ETD or EThcD experiments is the most promising data acquisition protocol.

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The fine tuning of hormone (e.g., auxin and gibberellin) levels and hormone signaling is required for maintaining normal embryogenesis.

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Certain apple cultivars accumulate to high levels in their nectar and stigma exudate an acidic chitinase III protein that can protect against pathogens including fire blight disease causing Erwinia amylovora. To prevent microbial infections, flower nectars and stigma exudates contain various antimicrobial compounds. Erwinia amylovora, the causing bacterium of the devastating fire blight apple disease, is the model pathogen that multiplies in flower secretions and infects through the nectaries.

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  • The establishment of seedlings after germination heavily relies on the regulation of plant hormones, particularly auxin, which plays a key role in processes like hypocotyl hook development.
  • The CRK5 protein kinase is crucial for regulating auxin transport during this process, and its mutation (At) leads to ineffective hypocotyl hook formation and reduced auxin accumulation on the concave side of the hook.
  • The study suggests that CRK5 may influence the function of specific auxin transport proteins (PIN3, PIN7, AUX1) through phosphorylation, ultimately affecting the balance of auxin and other hormones like ethylene and GA during hypocotyl development.
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  • Consensus sequences for posttranslational modifications like glycosylation suggest a possibility of modification but don't guarantee it occurs.
  • Different types of glycosylation (C-mannosylation, N-glycosylation, and O-glycosylation) involve specific amino acids and can vary widely in structure, making characterization complex.
  • Mass spectrometry, particularly LC/ESI-MS/MS, is the preferred method for analyzing the site-specific heterogeneity of glycosylation due to the variations in carbohydrate structures present in proteins.
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The roles of factor XIIIa-specific cross-links in thrombus formation, regression, or probability for embolization are largely unknown. A molecular understanding of fibrin architecture at the level of these cross-links could inform the development of therapeutic strategies to prevent the sequelae of thromboembolism. Here, we present an MS-based method to map native factor XIIIa cross-links in the insoluble matrix component of whole-blood or plasma-fibrin clots and in thrombi.

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Drosophila melanogaster sperm reach an extraordinary long size, 1.8 mm, by the end of spermatogenesis. The mitochondrial derivatives run along the entire flagellum and provide structural rigidity for flagellar movement, but its precise function and organization is incompletely understood.

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A relatively novel activation technique, electron-transfer/higher-energy collision dissociation (EThcD) was used in the LC-MS/MS analysis of tryptic glycopeptides enriched with wheat germ agglutinin from human urine samples. We focused on the characterization of mucin-type O-glycopeptides. EThcD in a single spectrum provided information on both the peptide modified and the glycan carried.

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Preeclampsia is a disease of the mother, fetus, and placenta, and the gaps in our understanding of the complex interactions among their respective disease pathways preclude successful treatment and prevention. The placenta has a key role in the pathogenesis of the terminal pathway characterized by exaggerated maternal systemic inflammation, generalized endothelial damage, hypertension, and proteinuria. This of preeclampsia may be triggered by distinct underlying mechanisms that occur at early stages of pregnancy and induce different phenotypes.

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A novel software, Pinnacle was used to reassess the reproducibility of a 2-step lectin-based O-glycopeptide enrichment method. A publicly available dataset consisting of 12 data files representing 3 technical replicates of enriched glycopeptides from human serum was investigated. Previously, an attempt for reproducibility assessment was made utilizing an MS/MS scan (MS2)-based method.

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