362 research outputs found
Electrospray ionization mass spectrometry as a tool to analyze hydrogen/deuterium exchange kinetics of transmembrane peptides in lipid bilayers
Quantitative Mass Spectrometry-based Proteomics
Mass spectrometry-based proteomics, the large-scale analysis of proteins by mass spectrometry, has emerged as a powerful technology over the past decade and has become an indispensable tool in many biomedical laboratories. Many strategies for differential proteomics have been developed in recent years, which involve either the incorporation of heavy stable isotopes or are based on label-free comparisons and their statistical assessment, and each of these has specific strengths and limitations. This chapter gives an overview of the current state-of-the-art in quantitative or differential proteomics and will be illustrated by several examples
Real-time modelling of indoor particulate matter concentration in poultry houses using broiler activity and ventilation rate
Measuring particulate matter concentration in poultry houses remains as a difficult task, primarily because aerosol analysers are expensive, require specialist knowledge to operate and are labour intensive to maintain. However, it is well known that high concentrations of particulate matter causes health and welfare problems with livestock, farm workers and people living in the vicinity of the farm premises. In this work, a data-based mechanistic model is developed to relate broiler activity and ventilation rate with indoor particulate matter concentration. For six complete growing cycles, in a U.K. commercial poultry farm, broiler activity was monitored using a camera-based flock monitoring system (eYeNamic®) and ventilation rate was measured. Indoor particulate matter concentration was continuously monitored by measuring size-segregated mass fraction concentrations with the aerosol analyser DustTrakTM. A discrete-time multi-input single-output time-invariant parameters Transfer Function model was developed to determine the particulate dynamics within each day of the growing cycle in the poultry house using broiler activity and ventilation rate as inputs. This model monitored indoor particulate matter concentration with an average accuracy of RT2=(51±26)%. A dynamic linear regression modelling with time-variant parameters improved average accuracy with RT2=(97.7±1.3)%. It forecasted one sample-ahead the indoor particulate matter concentration level, using a time window of 14 samples, with a mean relative prediction error, MRPE=(4.6±3.2)%. Thus, dynamic modelling with time-variant parameters has the potential to be part of a control system to manage in real-time indoor particulate matter concentration in broiler houses.status: publishe
Identification of Full-Length Wild-Type and Mutant Huntingtin Interacting Proteins by Crosslinking Immunoprecipitation in Mice Brain Cortex
Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways
Amyotrophic lateral sclerosis (ALS) is a devastating
neurological disease with no effective treatment
available. An increasing number of genetic causes of ALS
are being identified, but how these genetic defects lead to
motor neuron degeneration and to which extent they affect
common cellular pathways remains incompletely understood.
To address these questions, we performed an interactomic
analysis to identify binding partners of wild-type
(WT) and ALS-associated mutant versions of ATXN2,
C9orf72, FUS, OPTN, TDP-43 and UBQLN2 in neuronal
cells. This analysis identified several known but also many
novel binding partners of these proteins
Characterisation of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions
TBR1 is a neuron-specific transcription factor involved in brain development and implicated in a neurodevelopmental disorder (NDD) combining features of autism spectrum disorder (ASD), intellectual disability (ID) and speech delay. TBR1 has been previously shown to interact with a small number of transcription factors and co-factors also involved in NDDs (including CASK, FOXP1/2/4 and BCL11A), suggesting that the wider TBR1 interactome may have a significant bearing on normal and abnormal brain development. Here we have identified approximately 250 putative TBR1-interaction partners by affinity purification coupled to mass spectrometry. As well as known TBR1-interactors such as CASK, the identified partners include transcription factors and chromatin modifiers, along with ASD- and ID-related proteins. Five interaction candidates were independently validated using bioluminescence resonance energy transfer assays. We went on to test the interaction of these candidates with TBR1 protein variants implicated in cases of NDD. The assays uncovered disturbed interactions for NDD-associated variants and identified two distinct protein-binding domains of TBR1 that have essential roles in protein–protein interaction
Live cell transcription-coupled nucleotide excision repair dynamics revisited
Transcription–blocking lesions are specifically targeted by transcription-coupled nucleotide excision repair (TC-NER), which prevents DNA damage-induced cellular toxicity and maintains proper transcriptional processes. TC-NER is initiated by the stalling of RNA polymerase II (RNAPII), which triggers the assembly of TC-NER-specific proteins, namely CSB, CSA and UVSSA, which collectively control and drive TC-NER progression. Previous research has revealed molecular functions for these proteins, however, exact mechanisms governing the initiation and regulation of TC-NER, particularly at low UV doses have remained elusive, partly due to technical constraints. In this study, we employ knock-in cell lines designed to target the endogenous CSB gene locus with mClover, a GFP variant. Through live cell imaging, we uncover the intricate molecular dynamics of CSB in response to physiologically relevant UV doses. We showed that the DNA damage-induced association of CSB with chromatin is tightly regulated by the CSA-containing ubiquitin-ligase CRL complex (CRL4CSA). Combining the CSB-mClover knock-in cell line with SILAC-based GFP-mediated complex isolation and mass-spectrometry-based proteomics, revealed novel putative CSB interactors as well as discernible variations in complex composition during distinct stages of TC-NER progression. Our work not only provides molecular insight into TC-NER, but also illustrates the versatility of endogenously tagging fluorescent and affinity tags.</p
The dual role of LSD1 and HDAC3 in STAT5-dependent transcription is determined by protein interactions, binding affinities, motifs and genomic positions
STAT5 interacts with other factors to control transcription, and the mechanism of regulation is of interest as constitutive active STAT5 has been reported in malignancies. Here, LSD1 and HDAC3 were identified as novel STAT5a interacting partners in pro-B cells. Characterization of STAT5a, LSD1 and HDAC3 target genes by ChIP-seq and RNA-seq revealed gene subsets regulated by independent or combined action of the factors and LSD1/HDAC3 to play dual role in their activation or repression. Genes bound by STAT5a alone or in combination with weakly associated LSD1 or HDAC3 were enriched for the canonical STAT5a GAS motif, and such binding induced activation or repression. Strong STAT5 binding was see
The splicing factor XAB2 interacts with ERCC1-XPF and XPG for R-loop processing
RNA splicing, transcription and the DNA damage response are intriguingly linked in mammals but the underlying mechanisms remain poorly understood. Using an in vivo biotinylation tagging approach in mice, we show that the splicing factor XAB2 interacts with the core spliceosome and that it binds to spliceosomal U4 and U6 snRNAs and pre-mRNAs in developing livers. XAB2 depletion leads to aberrant intron retention, R-loop formation and DNA damage in cells. Studies in illudin S-treated cells and Csb(m/m) developing livers reveal that transcription-blocking DNA lesions trigger the release of XAB2 from all RNA targets tested. Immunoprecipitation studies reveal that XAB2 interacts with ERCC1-XPF and XPG endonucleases outside nucleotide excision repair and that the trimeric protein complex binds RNA:DNA hybrids under conditions that favor the formation of R-loops. Thus, XAB2 functionally links the spliceosomal response to DNA damage with R-loop processing with important ramifications for transcription-coupled DNA repair disorders
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