Biology subjects

Meier, N.

Publications and source records attributed to Meier, N..

7 recordsLinked to original sources

bioRxiv2025

In Situ, Antibody-Independent, and Multiplexed Characterization of Amyloid Plaques by MALDI MS/MS Imaging Using iprm-PASEF

BackgroundAmyloidosis collectively describes a heterogeneous group of protein aggregation-based diseases involving the misfolding and extracellular accumulation of fibril-forming amyloid proteins. The tissue deposition of these fibrils occurs either localized (limited to one organ) or systemically, impairing organ function and, in severe cases, leading to organ failure. Identification of the amyloidogenic protein leading to the correct subtyping is challenging but crucial for treatment decisions. Imaging parallel reaction monitoring (iprm)-parallel accumulation-serial fragmentation (PASEF) is a novel method for matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging (MSI) that enables the fast, spatially resolved, multiplexed, and antibody-independent identification of peptides and proteins in situ. In this proof-of-concept study, we demonstrate the applicability of iprm-PASEF for the in situ characterization of amyloidosis. MethodsA multiplexed iprm-PASEF panel (comprising trapped ion mobility spectrometry (TIMS) and m/z values) for characterizing amyloid plaques by MALDI-MSI was compiled. The panel included nine peptide entries of amyloidosis-associated proteins (vitronectin, apolipoprotein E, serum amyloid P component) and the prevalent amyloidosis-subtype proteins serum amyloid A, transthyretin, and immunoglobulin light chain 2. The multiplexed iprm-PASEF panel was applied to a tissue microarray (TMA) assembled from formalin-fixed, paraffin-embedded (FFPE) specimens, comprising biopsies of amyloidosis-positive tissues from 18 patients, including six different tissue types, and representing the following amyloidosis subtypes: ATTR (transthyretin amyloidosis), AL (immunoglobulin light chain amyloidosis), and AA (secondary amyloidosis). For comparison and co-localization, congo red staining was performed on adjacent slides. ResultsMALDI TIMS MS1 imaging was acquired from the amyloidosis TMA, providing an m/z feature list containing 1390 entries that was subsequently refined to only include m/z features likely stemming from amyloidosis-related peptides. Further, we focused on optimal usage of the m/z and ion mobility range to increase the number of targeted peptides. The final iprm-PASEF panel comprised 10 entries ranging from m/z 887.51 - 1,986.85 and 1/K0 1.4 - 2.1 V{middle dot}s/cm2; targeting nine peptides from six different amyloidosis-related proteins. Apolipoprotein E, serum amyloid P component, and immunoglobulin light chain 1/2 were included with two entries. Transthyretin, vitronectin, and serum amyloid A were covered by one peptide. One entry was included as a positive control targeting actin A. We applied the iprm-PASEF (MS2 mode) panel to the amyloidosis TMA and fragment (MS2) spectra were analyzed by the search engine MASCOT. Eight out of ten peptides derived from vitronectin, apolipoprotein E, serum amyloid A, serum amyloid P component, and transthyretin were successfully identified with MASCOT scores above 18. Comparison to Congo red staining indicated a more localized and heterogeneous pattern of amyloid-associated proteins (vitronectin, apolipoprotein E, serum amyloid P component) by iprm-PASEF. Compared to the clinical annotation, transthyretin and serum amyloid A were only found in their respective subtypes. In total, it was possible to describe the spatial distribution of five different amyloid-associated proteins, thereby further characterizing Congo red-positive amyloid plaques in one single iprm-PASEF measurement. Conclusion and perspectiveThis proof-of-concept study demonstrates feasibility for in situ, antibody-independent, and multiplexed proteomic typing of amyloidosis plaques. Future enlargement of the multiplex panel is likely to increase the number of targetable amyloid proteins and to probe for the presence of post-translational modifications. The present study highlights the value of iprm-PASEF for MALDI imaging strategies.

molecular biology↗

bioRxiv2025

TaWUS2D regulates the number of grains per spikelet by enhancing the number of fertile ovaries in Multi-Ovary Wheat

Innovative genetic improvements in the staple crop Triticum aestivum (bread wheat) are urgently needed to address the growing global food security crisis. Here, we report the map-based cloning of TaWUS2D, the gene responsible for the dominant multi-ovary phenotype in wheat. Multi-ovary lines are characterized by the development of three fertile ovaries per floret that results in three grains, as opposed to wildtype single ovary wheat. We used HiFi long-reads to assemble a 14.48 Gbp genome scaffold assembly in the background of mutli-ovary wheat line MOV. Using high-resolution genetic mapping, combined with additional genomic resources, we defined the Mov-1 locus to a 135 Kbp region containing two genes. Using five independent deletion mutants and eight TILLING mutants, we demonstrate that a functional WUSCHEL-like protein, TaWUS2D, is required for the multi-ovary phenotype. TaWUS2D is upregulated in the MOV genetic background. This research lays the groundwork for developing new approaches to improve wheat production potential and sustainability in the face of current and future global food challenges.

plant biology↗

bioRxiv2024

Longer Interstimulus Intervals Enhance Efficacy of Automated Phase-Targeted Auditory Stimulation on Procedural Memory Consolidation

Up-phase-targeted auditory stimulation (up-PTAS) during slow-wave sleep has become a valuable tool for modulating slow oscillations and slow-oscillation-spindle-coupling in favor of overnight memory retention. Developing effective, automated protocols for translation into more naturalistic or clinical settings is an ongoing challenge, especially given that current PTAS protocols and their behavioral effects vary greatly between different studies. Here, we assessed the electrophysiological and behavioral effects of systematically varying interstimulus intervals (ISIs) in automated up-PTAS in the home setting, using a mobile PTAS device and app-based behavioral tasks. Building on studies suggesting a non-linear relationship between stimulus number and PTAS effects, we show that applying fewer stimuli with longer ISIs enhanced overnight memory consolidation of a finger-tapping sequence more effectively than applying more stimuli with shorter ISIs. The behavioral response was predicted by the number of stimuli with auditory evoked K-complexes relative to the number of stimuli without K-complexes. PTAS stimuli applied at longer ISIs (> 1.25) were associated with a higher likelihood of K-complex responses and fast spindles nesting in the K-complex up-phase. Our results suggest that up-PTAS can be optimized for overnight memory consolidation by introducing ISIs of at least 1.25s. Our study highlights the feasibility of longitudinal at-home PTAS combined with app-based behavioral tasks in healthy participants while leveraging the mechanistic insights such data can offer. Statement of SignificancePhase-targeted auditory stimulation (PTAS) holds great promise for non-invasively enhancing essential functions of slow-wave sleep. However, current protocols have produced variable results and are often confined to laboratory settings. Our study demonstrates the feasibility of a mobile application of automated PTAS and provides experimental evidence that prolonging interstimulus intervals positively affects overnight procedural memory consolidation via K-complexes and coupled sleep spindles. As K-complexes may also be involved in cardiovascular function and brain waste clearance, the proposed protocol optimization may have effects beyond memory enhancement. Together, our findings lay a foundation for a broader application of PTAS in clinical longitudinal studies to improve patient care and recovery outcomes.

neuroscience↗

bioRxiv2024

Spatial Proteomics by Trapped Ion Mobility supported MALDI MS/MS Imaging: A First Glance into Multiplexed and Spatial Peptide Identification

RATIONALEIn spatial proteomics, matrix-assisted laser desorption/ionization (MALDI) imaging enables rapid and cost-effective peptide measurements. Yet, in situ peptide identification remains challenging. Therefore, this study aims to integrate the trapped ion mobility spectrometry (TIMS)-based parallel accumulation-serial fragmentation (PASEF) into MALDI imaging of tryptic peptides to enable multiplexed MS/MS imaging. METHODSAn initial MALDI TIMS MS1 survey measurement was performed, followed by a manual generation of a precursor list containing mass over charge values and ion mobility windows. Inside the dual TIMS system, submitted precursors were trapped, separately eluted by their ion mobility and analyzed in a quadrupole time-of-flight device, thereby enabling multiplexed MALDI MS/MS imaging. Finally, precursors were identified by peptide to spectrum matching. RESULTSThis study presents the first multiplexed MALDI TIMS MS/MS imaging (iprm-PASEF) of tryptic peptides. Its applicability was showcased on two histomorphologically distinct tissue specimens in a 4-plex and 5-plex setup. Precursors were successfully identified by the search engine MASCOT in one single MALDI imaging experiment for each respective tissue. Peptide identifications were corroborated by liquid-chromatography tandem mass spectrometry experiments and fragment co-localization analyses. CONCLUSIONSIn this study, we present a novel pipeline, based on iprm-PASEF that allows the multiplexed and spatial identification of tryptic peptides in MALDI imaging. Hence, it marks a first step towards the integration of MALDI imaging into the emerging field of spatial proteomics.

biochemistry↗

bioRxiv2022

High efficiency multiplex biallelic heritable editing in Arabidopsis using an RNA virus

Delivery of gene editing components such as the Cas nuclease and single guide RNAs (sgRNAs) into plant cells is commonly accomplished by agrobacterium-mediated transformation. Although Arabidopsis is easy to transform, generation of biallelic edited plants requires screening a large number of plants in subsequent generations. Here, we describe optimization of the Tobacco rattle virus (TRV) for in planta delivery of sgRNAs fused to a tRNAIleu that induces efficient multiplex somatic and biallelic heritable editing in Arabidopsis. Inclusion of tRNAIleu enhances the systemic movement of TRV and the mutant phenotype is visible in the initial TRV::sgRNA-tRNAIleu infected Arabidopsis, which allows for the uncovering of lethal phenotypes. Mutant progeny are recovered in the next generation (M1) at frequencies ranging from 30-60%, with 100% mutant recovery in the following (M2) generation. TRV::tRNAIleu system described here allows generation of biallelic edited plants in a single generation and is amenable for large-scale high throughput CRISPR screens.

plant biology↗

bioRxiv2021

New fossil wasp species from the earliest Eocene Fur Formation has its closest relatives in late Eocene ambers (Hymenoptera, Ichneumonidae, Pherhombinae)

Darwin wasps (Ichneumonidae) are one of the most species-rich insect families, but also one of the most understudied ones, both in terms of their extant and extinct diversity. We here use morphometrics of wing veins and an integrative Bayesian analysis to place a new rock fossil species from the Danish Fur Formation ([~]54 Ma) in the tree of Darwin wasps. The new species, Pherhombus parvulus n. sp., is placed firmly in Pherhombinae, an extinct subfamily so far only known from Baltic and Rovno-Ukranian ambers, which are estimated to be 34-48 Ma and 34-38 Ma, respectively. Our phylogenetic analysis recovers a subfamily clade within the higher Ophioniformes formed by Pherhombinae, Townesitinae and Hybrizontinae, in accordance with previous suggestions. Due to the placement of the new species as sister to the remaining members of Pherhombinae, we argue that our finding is not at odds with a much younger, late Eocene age ([~]34-41 Ma) of Baltic amber and instead demonstrates that Pherhombus existed over a much longer period than previously thought. Our results also exemplify the power of wing vein morphometrics and integrative phylogenetic analyses in resolving the placement even of poorly preserved fossil specimens.

paleontology↗

bioRxiv2020

A common molecular mechanism for cognitive deficits and craving in alcoholism

Alcohol-dependent patients commonly show impairments in executive functions that facilitate craving and can lead to relapse. The medial prefrontal cortex, a key brain region for executive control, is prone to alcohol-induced neuroadaptations. However, the molecular mechanisms leading to executive dysfunction in alcoholism are poorly understood. Here using a bi-directional neuromodulation approach we demonstrate a causal link for reduced prefrontal mGluR2 function and both impaired executive control and alcohol craving. By neuron-specific prefrontal knockdown of mGluR2 in rats, we generated a phenotype of reduced cognitive flexibility and excessive alcohol-seeking. Conversely, restoring prefrontal mGluR2 levels in alcohol-dependent rats rescued these pathological behaviors. Also targeting mGluR2 pharmacologically reduced relapse behavior. Finally, we developed a FDG-PET biomarker to identify those individuals that respond to mGluR2-based interventions. In conclusion, we identified a common molecular pathological mechanism for both executive dysfunction and alcohol craving, and provide a personalized mGluR2-mechanism-based intervention strategy for medication development of alcoholism.

neuroscience↗