Publications by authors named "Bamberger C"

Purpose: This study evaluates the hypothesis that a volumetric skin-sparing planning technique (SSPT) will reduce acute dermatitis in patients treated to the breast or chest wall (CW) with proton pencil-beam scanning (PBS).

Methods And Materials: In January 2022, our center incorporated volumetric-based skin-sparing objectives in addition to skin hot spot evaluation as an SSPT. The SSPT incorporated an objective to limit the volume of a skin evaluation structure (skin-eval) receiving 95% of the prescription dose or more (V95%Rx) to ideally < 50%.

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Mass spectrometry-based methods can provide a global expression profile and structural readout of proteins in complex systems. Preserving the in vivo conformation of proteins in their innate state is challenging during proteomic experiments. Here, we introduce a whole animal in vivo protein footprinting method using perfusion of reagents to add dimethyl labels to exposed lysine residues on intact proteins which provides information about protein conformation.

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Background: Neurosurgical cranial titanium mesh and screws are commonly encountered in postoperative radiation therapy. However, only a limited number of reports are available in the context of proton therapy, resulting in a lack of consensus among the proton centers regarding the protocol for handling the hardware.

Purpose: This study is to examine the impact of the hardware in proton plans.

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Article Synopsis
  • SARS-CoV-2, the virus responsible for COVID-19, infects human airway cells by binding its spike protein to the ACE2 receptor on those cells.
  • Researchers used advanced techniques to discover that the spike protein interacts with various host proteins, including laminin and thrombospondin, which could impact the virus's ability to infect cells.
  • The study found that specific proteins preferentially combined with the original D614 spike variant over the mutated G614 variant, suggesting that this could allow the virus to infect a wider range of cells beyond just those that express ACE2.
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  • Researchers have developed a new method called covalent protein painting (CPP) to investigate protein structure and expression changes in the context of Alzheimer's disease (AD) using intact animals.
  • This study found that structural changes in proteins related to energy generation, carbon metabolism, and metal ion homeostasis occur before any changes in protein expression as AD progresses.
  • The analysis revealed that certain pathways with structural changes were significantly co-regulated across different organs, including the brain, kidney, muscle, and spleen.
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Analogous to articular cartilage, changes in spatial chondrocyte organisation have been proposed to be a strong indicator for local tissue degeneration in the intervertebral disc (IVD). While a progressive structural and functional degradation of the extracellular (ECM) and pericellular (PCM) matrix occurs in osteoarthritic cartilage, these processes have not yet been biomechanically elucidated in the IVD. We aimed to evaluate the local stiffness of the ECM and PCM in the anulus fibrosus of the IVD on the basis of local chondrocyte spatial organisation.

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The transcription factors p63 and p73 have high similarity to the tumor suppressor protein p53. While the importance of p53 in DNA damage control is established, the functions of p63 or p73 remain elusive. Here, we analyzed nvp63, the cnidarian homologue of p63, that is expressed in the mesenteries of the starlet sea anemone and that is activated in response to DNA damage.

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During tumorigenesis, DNA mutations in protein coding sequences can alter amino acid sequences which can change the structures of proteins. While the 3D structure of mutated proteins has been studied with atomic resolution, the precise impact of somatic mutations on the 3D proteome during malignant transformation remains unknown because methods to reveal protein structures in high throughput are limited. Here, we measured the accessibility of the lysine ε-amine for chemical modification across proteomes using covalent protein painting (CPP) to indirectly determine alterations in the 3D proteome.

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The tumor suppressor p53-like protein p63 is required for self-renewal of epidermal tissues. Loss of p63 or exposure to ultraviolet (UV) irradiation triggers terminal differentiation in keratinocytes. However, it remains unclear how p63 diverts epidermal cells from proliferation to terminal differentiation, thereby contributing to successful tissue self-renewal.

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Article Synopsis
  • Misfolding and aggregation of amyloid-β and hyperphosphorylated tau are key indicators of Alzheimer's disease, but current methods can't track protein folding throughout the entire proteome in AD.
  • The study introduces covalent protein painting (CPP), a mass spectrometry technique that measures how accessible specific lysine residues are on proteins, revealing changes in their structure in response to conditions like heat shock.
  • Analysis of human brain tissue indicates that the structural changes in proteins such as tubulin-β and succinate dehydrogenase in patients with neurodegenerative diseases suggest broader disruptions in protein structures beyond just amyloid-β and tau.
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The SARS-CoV-2 virus causes severe acute respiratory syndrome (COVID-19) and has rapidly created a global pandemic. Patients that survive may face a slow recovery with long lasting side effects that can afflict different organs. SARS-CoV-2 primarily infects epithelial airway cells that express the host entry receptor Angiotensin Converting Enzyme 2 (ACE2) which binds to spike protein trimers on the surface of SARS-CoV-2 virions.

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Accumulation of aggregated amyloid beta (Aβ) in the brain is believed to impair multiple cellular pathways and play a central role in Alzheimer's disease pathology. However, how this process is regulated remains unclear. In theory, measuring protein synthesis is the most direct way to evaluate a cell's response to stimuli, but to date, there have been few reliable methods to do this.

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The multistep process regulating the maturation of membrane proteins in the endoplasmic reticulum (ER) and the secretory pathway is disrupted in many protein misfolding disorders. Mutations in the ion channel CFTR that impair its folding and subsequent localization to the plasma membrane cause cystic fibrosis (CF), an inherited and eventually lethal disease that impairs the function of multiple organs, mostly the lungs. Here, we found that proper maturation of CFTR is dependent on cross-talk between phosphorylation and methylation events in the regulatory insertion (RI) element of the protein.

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Article Synopsis
  • Mammalian cells have various compartments that create specialized environments, enabling different biological processes to occur at the same time.
  • Proteins are directed to specific subcellular locations where they perform unique functions based on their compartment.
  • Spatial proteomics is a method used to identify and measure the location of proteins within these subcellular structures.
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The human genome harbors just 20,000 genes suggesting that the variety of possible protein products per gene plays a significant role in generating functional diversity. In bottom-up proteomics peptides are mapped back to proteins and proteoforms to describe a proteome; however, accurate quantitation of proteoforms is challenging due to incomplete protein sequence coverage and mapping ambiguities. Here, we demonstrate that a new software tool called ProteinClusterQuant (PCQ) can be used to deduce the presence of proteoforms that would have otherwise been missed, as exemplified in a proteomic comparison of two fly species, Drosophila melanogaster and D.

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To maximize the chances of replacing smoking with vaping, it is necessary to know the different types of existing devices, their characteristics and their most important settings as well as their influence on sensations. To support a user it is also important to understand the nature of the inhaled and exhaled vapor, as well as the possible mistakes that can lead to a less enjoyable experience. Highlighting e-liquids formulations and emissions can help understanding how a minimum of 95 % risk reduction compared to tobacco smoking is achieved and the influence of compounds on the user's experience.

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Regular walnut consumption is associated with better health. We have previously shown that eight weeks of walnut consumption (43 g/day) significantly improves lipids in healthy subjects. In the same study, gut microbiome was evaluated.

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Cellular proteomes are thought to be optimized for function, leaving no room for proteome plasticity and, thus, evolution. However, hybrid animals that result from a viable cross of two different species harbor hybrid proteomes of unknown complexity. We charted the hybrid proteome of a viable cross between females and males with bottom-up proteomics.

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Unlabelled: Studies indicate a positive association between walnut intake and improvements in plasma lipids. We evaluated the effect of an isocaloric replacement of macronutrients with walnuts and the time point of consumption on plasma lipids. We included 194 healthy subjects (134 females, age 63 ± 7 years, BMI 25.

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Objective Venous stasis is a risk factor for venous thromboembolism. We aimed to determine the efficacy of forceful foot exercises for actuation of the calf muscle pump to counteract stasis. Methods We examined 20 seated healthy subjects.

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Article Synopsis
  • Affinity purification coupled to mass spectrometry (AP-MS) often misses identifying dynamic protein-protein interactions, especially with membrane proteins, leading to low bait yields.
  • The new method CoPIT (co-interacting protein identification technology) enhances the analysis of membrane protein interactomes, integrating experimental and computational techniques for better identification and visualization of protein interactions.
  • CoPIT shows significant improvements with up to 100-fold higher bait yield for membrane proteins like CFTR, while also being applicable to various protein types; the entire experimental process takes less than 3 days, but data analysis may take weeks.
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Deletion of phenylalanine 508 of the cystic fibrosis transmembrane conductance regulator (∆F508 CFTR) is the major cause of cystic fibrosis, one of the most common inherited childhood diseases. The mutated CFTR anion channel is not fully glycosylated and shows minimal activity in bronchial epithelial cells of patients with cystic fibrosis. Low temperature or inhibition of histone deacetylases can partly rescue ∆F508 CFTR cellular processing defects and function.

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  • Chemical labeling of peptides enhances protein quantification in shotgun proteomics, independent of the sample source.
  • Current methods using isobaric labels often suffer from inaccurate ratio measurements due to the presence of contaminating peptides.
  • A new technique measures isobaric peptide fragment isotopologues, improving quantification precision and achieving over 90% protein detection in MudPIT experiments, including accurate measurements in cystic fibrosis cell lines.
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