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Schwartz, D.

Publications and source records attributed to Schwartz, D..

At least 19 recordsLinked to original sources

Scaling a context-aware genomic model for condition-specific edit design in plants

Engineering agronomically relevant traits in crops often requires changing a gene's activity in a specific tissue, developmental stage or environmental condition while preserving its roles in other contexts. Designing such selective changes requires predicting how cis-regulatory sequences are interpreted in different biological states, as the same edit can have different effects across contexts. Genomic models have made substantial progress in predicting gene expression from DNA sequence, yet sequence-only predictors do not receive an explicit description of biological states. We introduce CROP-1 (Context-aware Regulatory Output Prediction model), which combines DNA sequence with transcription factor binding motifs and measured expression to predict gene activity as a function of both sequence and regulatory state. On a held-out test set spanning six plant species, CROP-1 achieves a median per-gene Pearson correlation across contexts of 0.831, compared with 0.486 for its parameter-matched sequence-only counterpart, and 57-246% higher median correlations than three genomic foundation models fully fine-tuned on the same task. Prediction accuracy also improves with scale: increasing model capacity reduces validation error by 48%, while expanding training data to include more diverse biological contexts reduces it by 58%. We then use gradient-based sequence optimisation to translate a desired gene expression pattern into candidate edits of its cis-regulatory sequence, targeting up- or down-regulation in one context while preserving expression in others. In soybean and tomato, edit designs with 1-20 nucleotide substitutions produce strong predicted target responses and much smaller average changes across non-target contexts. By connecting scalable learning of sequence-state relationships to selective edit design, CROP-1 provides a computational foundation for controlling where, when and under which conditions endogenous crop genes are active.

plant biology↗

Detecting movement preparation with HYDRE: a hybrid model of temporal and spectral brain signals

Previous research on brain-computer interfaces (BCIs) has demonstrated the feasibility of decoding different movements. However, less attention has been given to detecting motor preparation (i.e., decoding from brain signals whether or not a participant is about to perform a given movement). In this study, we wanted to assess the performance of a new model, rooted in motor preparation physiology, in detecting an upcoming movement across the period preceding a voluntary action. Participants (n=18, including 7 females) performed a simple self-paced motor task where they either pressed a button to change an image shown on screen, or let the computer change the image. Participants' brain activity was recorded using magnetoencephalography and submitted to a newly developed linear ensemble classifier that relies on features extracted using PCA from the temporal, spectral and Riemannian domain. We then compared its performance against other classifiers used in BCIs. Our HYbrid Domain Riemannian Ensemble (HYDRE) classifier emerged as the best-performing method, achieving average above-chance decoding up to 1400ms before the action, with a maximum ROC score of 76% at the time of the button press. Moreover, decoding performance in the temporal and Riemannian domains was respectively predictive of Readiness Field and Event-Related Desynchronization magnitudes, two well-known motor preparation markers. Combining features from the temporal, spectral, and Riemannian domains significantly improved motor preparation decoding compared to single-domain approaches. By leveraging the most discriminative features from each domain, HYDRE yielded consistent performance gains across participants with varying baseline decoding performance, effectively addressing inter-individual variability in motor preparation markers.

neuroscience↗

NicheProt: Cell-type-resolved proteomics of tissue compartments

Spatial proteomics uncovers the molecular underpinnings of cellular function in intact tissues. Laser capture microdissection coupled with mass spectrometry enables comprehensive proteomic profiling of selected tissue regions, but typically does not support cell-type-specific proteomic analysis. We present NicheProt, a 3D optical microscopy-guided, photobleaching-mediated cell barcoding approach for isolating intact specific cell types from defined microanatomical tissue compartments or niches. Using sequential bottom-up proteomic analysis, we defined two distinct phenotypes of CD11c dendritic cells based on their spatial locations in the inflamed mouse spleen. These two compartment-specific dendritic cell populations were characterized by proteomic signatures differing in the levels of 54 proteins. This 3D tissue microscopy-guided method offers cell-type and microregion-resolved proteomic analysis, facilitating the proteomic discovery of previously unrecognized cell subtypes and their functional roles in distinct tissue compartments.

systems biology↗

The Mismatch Negativity compared: EEG, SQUID-MEG and novel 4Helium-OPMs

Magneto-encephalography (MEG) provides a higher spatial resolution than electro-encephalography (EEG) to measure human auditory responses. However, conventional cryogenic MEG systems (SQUID-MEG) suffer from severe technological restrictions limiting, for instance, routine clinical use. Fortunately, a new generation of MEG sensors, optically pumped magnetometers (OPMs), have been developed to bridge the gap, combining the wearability of EEG with the benefits of MEG signal acquisition. We aim to assess their potential for studying auditory mismatch processing. The auditory Mismatch Negativity (MMN) is a well-characterized evoked component observable using a passive oddball paradigm with two-tone sound sequences. It has been extensively described using both EEG and MEG and is part of many EEG-based clinical applications, such as the assessment of patients with disorders of consciousness. MMN is therefore a relevant candidate to evaluate OPM performance. We use recently developed Helium-OPMs, which are high dynamic range MEG sensors that operate at room temperature. We compare their performance with cryogenic SQUID-MEG and EEG in a passive frequency oddball paradigm. Results show a significant MMN across subjects in all modalities as well as a high temporal similarity between modalities. Signal-to-noise ratios were also similar, and detection of significant individual MMN (within-subjects) using the OPM system was equal or better than EEG. Given that the OPM system tested here is a prototype comprised of only five sensors, these results are a promising step towards wearable MEG that combines the advantages of MEG and EEG.

neuroscience↗

Emergence of Pre-movement Beta Activity with Stable Sensorimotor Predictions to Facilitate Motor Adjustments

Adaptive behavior enables flexible responses to environmental changes. This process is particularly crucial when transitioning between environments with different features, relying on the progressive formation of expectations based on prior experience. In humans, beta oscillations are central to adaptive behavior. Yet, the brain mechanisms underlying the detection of environmental changes, and the iterative update needed to progressively improve behavioral performance remain elusive. Here, we reveal that beta activity emerges in a cerebello-cortical network two seconds before action initiation, as the features of a new environment become known and behavioral outcomes become more predictable. Within this period, the cerebellum and parietal cortex drive prefrontal activity to form expectations. Using a single-trial approach, we establish that beta bursts before action initiation predict performance in the upcoming trial based on previous outcomes. These findings uncover a novel anticipatory mechanism that reflects predictive processes critical for stabilizing performance and adapting to environmental changes.

neuroscience↗

NIRSTORM: a Brainstorm extension dedicated to functional Near Infrared Spectroscopy (fNIRS) data analysis, advanced 3D reconstructions, and optimal probe design.

SignificanceWe propose NIRSTORM, a software package built within Brainstorm environment, enabling full data analysis of functional Near InfraRed Spectroscopy (fNIRS) data from experiment planning to 3D reconstruction of hemodynamic fluctuations on the cortical surface using optical tomographic approaches. NIRSTORM enables the integration of fNIRS analysis within a multimodal setup making it easy to study fNIRS in combination with other multimodal data such as electroencephalography (EEG) or magnetic resonance imaging (MRI). AimNIRSTORM aims to provide an easy-to-use and fully modular toolbox for fNIRS analysis from experimental planning to optical tomography 3D reconstruction extending Brainstorm capacity for multimodal analysis. ApproachNIRSTORM was developed in MATLAB(R) and integrated as a plugin of the software Brainstorm. Brainstorm is a GUI-oriented, widely used software originally dedicated to statistical analysis and source imaging of EEG and magnetoencephalography (MEG) data. ResultsIn addition to conventional fNIRS preprocessing steps, including standard channel space and statistical analyses, NIRSTORM provides advanced methods dedicated to optimal probe placement, allowing personalized fNIRS study designs and accurate near-infrared optical tomography within the Maximum Entropy on the Mean (MEM) framework. ConclusionNIRSTORM is an open-access, user-friendly plugin extending the capacity of Brainstorm, for fNIRS analysis, therefore narrowing the gap between EEG/MEG and hemodynamics.

bioengineering↗

Transposable elements are entangled in rapid adaptation to climate change

Biodiversity conservation is urged at biodiversity hotspots that are under constant threat from anthropogenic development, yet a careful examination of the adaptive potential is a prerequisite for action. The Levant is considered a biodiversity hotspot and the distribution edge for many species, including important crop wild relatives. This region is under accelerated desertification and constantly disturbed by human activities, thus urging intervenient action. We collected and sequenced 300 wild barley plants along an eco-geographic gradient following a unique ecological-genetic sampling design. This scheme enabled to overcome the tight correlation between environmental and geographic distances. Phenotypic data was collected from 3600 progeny plants over three years and enabled to identify adaptive haplotype blocks comprised of phenological regulating genes tightly linked to drought and heat responsive genes. These haplotype blocks were highly enriched for transposable elements insertions, likely regulating genetic variation around adaptive genes, especially in stressed populations. Ecological and evolutionary models using over 2600 observations were combined to predict maladaptive risk, indicating that populations will be funneled into higher water availability refugia habitats while increasing isolation. Our findings highlight the main factors affecting rapid local adaptation and provide important recommendations for biodiversity management and conservation.

plant biology↗

Phage infection fronts trigger early sporulation and collective defense in bacterial populations

I.Bacteriophage (phage) infect, lyse, and propagate within bacterial populations. However, physiological changes in bacterial cell state can protect against infection even within genetically susceptible populations. One such example is the generation of endospores by Bacillus and its relatives, characterized by a reversible state of reduced metabolic activity that protects cells against stressors including desiccation, energy limitation, antibiotics, and infection by phage. Here we tested how sporulation at the cellular scale impacts phage dynamics at population scales when propagating amongst B. subtilis in spatially structured environments. Initially, we found that plaques resulting from infection and lysis were approximately 3-fold smaller on lawns of sporulating wild-type bacteria vs. non-sporulating bacteria. Notably, plaque size was reduced due to an early termination of expanding phage plaques rather than the reduction of plaque growth speed. Microscopic imaging of the plaques revealed sporulation rings, i.e., spores enriched around plaque edges relative to phage-free regions. We developed a series of mathematical models of phage, bacteria, spore, and small molecules that recapitulate plaque dynamics and identify a putative mechanism: sporulation rings arise in response to lytic activity. In aggregate, sporulation rings inhibit phage from accessing susceptible cells even when sufficient resources are available for further infection and lysis. Together, our findings identify how dormancy can self-limit phage infections at population scales, opening new avenues to explore the entangled fates of phages and their bacterial hosts in environmental and therapeutic contexts.

microbiology↗

Auditory selective attention during a working memory task with melodies: a MEG study

Working memory and attention are jointly needed in most everyday life tasks and activities. They have however mostly been studied separately. Here we investigate how auditory working memory and selective attention interact using a recently introduced paradigm (MEMAT) that combines a classic working memory paradigm, the delayed-matching-to-sample task, and selective attention, with distractors presented during the encoding phase. All stimuli are four-tone melodies. Twenty-two participants performed the MEMAT task during MEG recordings. We manipulate the difficulty of the memory task and of attentional filtering. When memory task difficulty increases, the amplitude of the CNV in anticipation of the melody to encode increases and the decrease in alpha power during encoding and maintenance in a left fronto-temporal network is reduced. When attentional filtering difficulty increases, the amplitude of the sustained evoked response during encoding increases, whereas the differential processing of relevant and irrelevant sounds in auditory areas is less pronounced, and frontal theta power during encoding and maintenance is higher. In the left auditory cortex, we could directly observe the result of the interaction between auditory memory and attention: the facilitation of relevant sound processing in the easy filtering condition was reduced when the memory task difficulty increased. This pattern mirrors the observed behavioral effects. Overall brain dynamics highlight reciprocal influences of working memory and selective attention processes, in keeping with shared cognitive resources between them.

neuroscience↗

Enlarged Perivascular Spaces are Associated with White Matter Injury, Brain Atrophy, Cognitive Decline and Markers of Inflammation in an Autosomal Dominant Vascular Neurodegenerative Disease (CADASIL)

Background and ObjectivesEnlarged perivascular spaces (ePVS) have been previously reported in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy (CADASIL), but their significance and pathophysiology remains unclear. We investigated associations of ePVS with classical imaging measures, cognitive measures and plasma proteins to better understand what ePVS represents in CADASIL and whether radiographic measures of ePVS would be of value in future therapeutic discovery studies for CADASIL. Methods24 individuals with CADASIL and 24 age and sex matched controls were included. Disease status was determined based on presence of NOTCH3 mutation. Brain imaging measures of white matter hyperintensity (WMH), brain parenchymal fraction (BPF), ePVS volumes, clinical, and cognitive measures, as well as plasma proteomics were used in models. Global ePVS volumes were calculated via a novel, semi-automated pipeline and levels of 7363 proteins were quantified in plasma using the SomaScan assay. The relationship of ePVS with global burden of WMH, brain atrophy, functional status, neurocognitive measures, and plasma proteins were modelled with linear regression models. ResultsCADASIL and control groups did not exhibit differences in mean ePVS volumes. However, increased ePVS volumes in CADASIL were associated with increased WMH volume ({beta}=0.57, p=0.05), Clinical Dementia Rating (CDR) Sum-of-Boxes score ({beta}=0.49, p=0.04), and decreased brain parenchymal fraction (BPF) ({beta}=-0.03, p=0.10). In interaction term models, the interaction term between CADASIL disease status and ePVS volume was associated with increased WMH volume ({beta}=0.57, p=0.02), Clinical Dementia Rating (CDR) Sum-of-Boxes score ({beta}=0.52, p=0.02), decreased BPF ({beta}=-0.03, p=0.07) and Mini Mental State Examination (MMSE) score ({beta}=-1.49, p=0.03). Proteins positively associated with ePVS volumes were found to be related to leukocyte migration and inflammation, while negatively associated proteins were related to lipid metabolism. Two central hub proteins were identified in protein networks associated with ePVS volumes: CXCL8/IL-8, and CCL2/MCP-1. The levels of CXCL8/IL8 were also associated with increased WMH volume ({beta}=2.44, p < 0.01), and levels of CCL2/MCP-1 were further associated with decreased BPF ({beta}=-0.0007, p < 0.01), MMSE score ({beta}=-0.02, p < 0.01), and increased Trail Making Test B (TRAILB) completion time ({beta}=0.76, p < 0.01). No protein was associated with all 3 studied imaging measures of pathology (BPF,ePVS,WMH). DiscussionBased on associations uncovered between ePVS volumes and cognitive functions, imaging and plasma proteins, we conclude that ePVS volumes capture pathologies contributing to chronic brain dysfunction and degeneration in CADASIL, with relevance to future clinical trials for novel therapeutic discoveries to prevent decline and injury in individuals carrying NOTCH3 mutations.

neuroscience↗

Human-gut phages harbor sporulation genes

Spore-forming bacteria are prevalent in mammalian guts and have implications for host health and nutrition. The production of dormant spores is thought to play an important role in the colonization, persistence, and transmission of these bacteria. Spore formation also modifies interactions among microorganisms such as infection by phages. Recent studies suggest that phages may counter dormancy-mediated defense through the expression of phage-encoded sporulation genes during infection, which can alter the transitions between active and inactive states. By mining genomes and gut-derived metagenomes, we identified sporulation genes that are preferentially encoded by phages that infect spore-forming bacteria. These included genes involved in chromosome partitioning, DNA damage repair, and cell wall-associated functions. In addition, phages contained homologs of sporulation-specific transcription factors, notably spo0A, the master regulator of sporulation, which could allow phages to control the complex genetic network responsible for spore development. Our findings suggest that phages could influence the formation of bacterial spores with implications for the health of the human gut microbiome, as well as bacterial communities in other environments. SIGNIFICANCEPhages acquire bacterial genes and use them to alter host metabolism in ways that enhance their fitness. To date, most auxiliary genes replace or modulate enzymes that are used by the host for nutrition or energy production. However, phage fitness is affected by all aspects of host physiology, including decisions that reduce metabolic activity of the cell. Here we focus on endosporulation, a complex and ancient form of dormancy found among the Bacillota that involves hundreds of genes. By coupling homology searches with host classification, we identify 31 phage-encoded homologs of sporulation genes that are mostly limited to phages infecting spore-forming bacteria. Nearly one-third the homologs recovered were regulatory genes suggesting that phages may manipulate host genetic networks by tapping into their control elements. Our findings also suggest a mechanism by which phages can overcome the defensive strategy of dormancy, which may be involved in coevolutionary dynamics of spore-forming bacteria.

microbiology↗

Diverse beta burst waveform motifs characterize movement-related cortical dynamics

Classical analyses of induced, frequency-specific neural activity typically average bandlimited power over trials. More recently, it has become widely appreciated that in individual trials, beta band activity occurs as transient bursts rather than amplitude-modulated oscillations. Most studies of beta bursts treat them as unitary, and having a stereotyped waveform. However, we show there is a wide diversity of burst shapes. Using a biophysical model of burst generation, we demonstrate that waveform variability is predicted by variability in the synaptic drives that generate beta bursts. We then use a novel, adaptive burst detection algorithm to identify bursts from human MEG sensor data recorded during a joystick-based reaching task, and apply principal component analysis to burst waveforms to define a set of dimensions, or motifs, that best explain waveform variance. Finally, we show that bursts with a particular range of waveform motifs, ones not fully accounted for by the biophysical model, differentially contribute to movement-related beta dynamics. Sensorimotor beta bursts are therefore not homogeneous events and likely reflect distinct computational processes.

neuroscience↗

Optimal dormancy strategies in fluctuating environments given delays in phenotypic switching

Organisms have evolved different mechanisms in response to periods of environmental stress, including dormancy - a reversible state of reduced metabolic activity. Transitions to and from dormancy can be random or induced by changes in environmental conditions. Prior theoretical work has shown that stochastic transitioning between active and dormant states at the individual level can maximize fitness at the population level. However, such theories of bet-hedging strategies typically neglect certain physiological features of transitions to dormancy, including time lags to gain protective benefits. Here, we construct and analyze a dynamic model that couples stochastic changes in environmental state with the population dynamics of organisms that can initiate dormancy after an explicit time delay. Stochastic environments are simulated using a multi-state Markov chain through which the mean and variance of environmental residence time can be adjusted. In the absence of time lags (or in the limit of very short lags), we find that bet-hedging strategy transition probabilities scale inversely with the mean environmental residence times, consistent with prior theory. We also find that increasing delays in dormancy decreases optimal transitioning probabilities, an effect that can be influenced by the correlations of environmental noise. When environmental residence times - either good or bad - are uncorrelated, the maximum population level fitness is obtained given low levels of transitioning between active and dormant states. However when environmental residence times are correlated, optimal dormancy initiation and termination probabilities increase insofar as the mean environmental persistent time is longer than the delay to reach dormancy. We also find that bet hedging is no longer advantageous when delays to enter dormancy exceed the mean environmental residence times. Altogether, these results show how physiological limits to dormancy and environmental dynamics shape the evolutionary benefits and even viability of bet hedging strategies at population scales.

ecology↗

Measuring brain critical dynamics to inform Brain-Computer Interfaces

Large-scale interactions among multiple brain regions manifest as bursts of activations called neuronal avalanches, which reconfigure according to the task at hand and, hence, might constitute natural candidates to design brain-computer interfaces (BCI). To test this hypothesis, we used source-reconstructed magneto/electroencephalography, during resting state and a motor imagery task performed within a BCI protocol. To track the probability that an avalanche would spread across any two regions we built an avalanche transition matrix (ATM) and demonstrated that the edges whose transition probabilities significantly differed between conditions hinged selectively on premotor regions in all subjects. Furthermore, we showed that the topology of the ATMs allows task-decoding above the current gold standard. Hence, our results suggest that Neuronal Avalanches might capture interpretable differences between tasks that can be used to inform brain-computer interfaces.

neuroscience↗

RADGENNETS: DEEP LEARNING-BASED RADIOGENOMICS MODEL FOR GENE MUTATION PREDICTION IN LUNG CANCER

AO_SCPLOWBSTRACTC_SCPLOWIn this paper, we present our methodology that can be used for predicting gene mutation in patients with non-small cell lung cancer (NSCLC). There are three major types of gene mutations that a NSCLC patients gene structure can change to: epidermal growth factor receptor (EGFR), Kirsten rat sarcoma virus (KRAS), and Anaplastic lymphoma kinase (ALK). We worked with the clinical and genomics data for each patient as well CT scans. We preprocessed all of the data and then built a novel pipeline to integrate both the image and tabular data. We built a novel pipeline that used a fusion of Convolutional Neural Networks and Dense Neural Networks. Also, using a search approach, we pick an ensemble of deep learning models to classify the separate gene mutations. These models include EfficientNets, SENet, and ResNeXt WSL, among others. Our model achieved a high area under curve (AUC) score of 94% in detecting gene mutation.

cancer biology↗

Theta band-power shapes amyloid-driven longitudinal EEG changes in pre-clinical Alzheimer's Disease

Alzheimers Disease (AD) includes progressive symptoms spread along a continuum of pre-clinical (pre-AD) and clinical stages. Pre-AD refers to cognitively healthy individuals with presence of positive pathophysiological biomarkers of AD (i.e., markers of amyloidopathy and tauopathy). Although numerous studies uncovered the neuro-cognitive changes of AD, very little is known on the natural history of brain lesions and modifications of brain networks of pre-AD. To address this issue, we analysed resting-state EEG data of 318 cognitively healthy individuals with subjective memory complains from the INSIGHT-preAD cohort at the time of their first visit (M0) and two-years later (M24). Using 18F-florbetapir PET-scanner, subjects were stratified between amyloid positive (A-; n=230) and amyloid negative (A+; n=88) groups. Differences between A+ and A- individuals were estimated at source level in each band of the EEG power spectrum. At M0, we found an increase of theta-band power in the mid-frontal cortex in A+ compared to A-. No significant association was found between mid-frontal theta power and the individuals cognitive performance. While the very same effect was not replicated at M24, theta-band power increased in A+ relative to A- individuals in the posterior cingulate cortex and the pre-cuneus. Furthermore, alpha band revealed a peculiar decremental trend in posterior brain regions in the A+ relative to the A- group only at M24. These results provide the first source-level longitudinal evidence on the impact of brain amyloidosis on the EEG dynamics of a large-scale, monocentric cohort of pre-AD. Theta-band power increase over the mid-frontal and mid-posterior cortices suggests an hypoactivation of the default-mode network in individuals at-risk of AD and a non-linear longitudinal progression of the AD-spectrum.

neuroscience↗

MRI-Visible Perivascular Space (PVS) Changes with Long-Duration Spaceflight

Humans are exposed to extreme environmental stressors during spaceflight and return with alterations in brain structure and shifts in intracranial fluids. To date, no studies have evaluated the effects of spaceflight on perivascular spaces (PVSs) within the brain, which are believed to facilitate fluid drainage and brain homeostasis. Here, we examined how the number and morphology of magnetic resonance imaging (MRI)-visible PVSs are affected by spaceflight, including prior spaceflight experience. Fifteen astronauts underwent six T1-weighted 3T MRI scans, twice prior to launch and four times following their return to Earth after [~]6-month missions to the International Space Station. White matter MRI-visible PVS number and morphology were calculated using an established automated segmentation algorithm. We found that novice astronauts showed an increase in total PVS volume from pre- to post-flight, whereas experienced crewmembers did not (adjusted for age, sex, and time between landing and first MRI scan). Moreover, experienced astronauts exhibited a significant correlation between more previous flight days and greater PVS median length at baseline, suggesting that experienced astronauts exhibit holdover effects from prior spaceflight(s). There was also a significant positive correlation between pre- to post-flight increases in PVS median length and increases in right lateral ventricular volume. The presence of spaceflight associated neuro-ocular syndrome (SANS) was not associated with PVS number or morphology. Together, these findings demonstrate that spaceflight is associated with PVS morphological changes, and specifically that spaceflight experience is an important factor in determining PVS characteristics.

neuroscience↗

The Okur-Chung Neurodevelopmental Syndrome (OCNDS) mutation CK2K198R leads to a rewiring of kinase specificity

Okur-Chung Neurodevelopmental Syndrome (OCNDS) is caused by heterozygous mutations to the CSNK2A1 gene, which encodes the alpha subunit of casein kinase II (CK2). The most frequently occurring mutation is lysine 198 to arginine (K198R). To investigate the impact of this mutation, we first generated a high-resolution phosphorylation motif of CK2WT, including the first characterization of specificity for tyrosine phosphorylation activity. A second high resolution motif representing CK2K198R substrate specificity was also generated. Here we report for the first time the impact of the OCNDS associated CK2K198R mutation. Contrary to prior speculation, the mutation does not result in a loss of function, but rather shifts the substrate specificity of the kinase. Broadly speaking the mutation leads to 1) a decreased preference for acidic residues in the +1 position, 2) a decreased preference for threonine phosphorylation, 3) an increased preference for tyrosine phosphorylation, and 4) an alteration of the tyrosine phosphorylation specificity motif. To further investigate the result of this mutation we have developed a probability-based scoring method, allowing us to predict shifts in phosphorylation in the K198R mutant relative to the wild type kinase. As an initial step we have applied the methodology to the set of axonally localized ion channels in an effort to uncover potential alterations of the phosphoproteome associated with the OCNDS disease condition.

neuroscience↗