ABSTRACT
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
ABSTRACT
Protein aggregation and abnormal lipid homeostasis are both implicated in neurodegeneration through unknown mechanisms. Here we demonstrate that aggregate-membrane interaction is critical to induce a form of cell death called ferroptosis. Importantly, the aggregate-membrane interaction that drives ferroptosis depends both on the conformational structure of the aggregate, as well as the oxidation state of the lipid membrane. We generated human stem cell-derived models of synucleinopathy, characterized by the intracellular formation of α-synuclein aggregates that bind to membranes. In human iPSC-derived neurons with SNCA triplication, physiological concentrations of glutamate and dopamine induce abnormal calcium signaling owing to the incorporation of excess α-synuclein oligomers into membranes, leading to altered membrane conductance and abnormal calcium influx. α-synuclein oligomers further induce lipid peroxidation. Targeted inhibition of lipid peroxidation prevents the aggregate-membrane interaction, abolishes aberrant calcium fluxes, and restores physiological calcium signaling. Inhibition of lipid peroxidation, and reduction of iron-dependent accumulation of free radicals, further prevents oligomer-induced toxicity in human neurons. In summary, we report that peroxidation of polyunsaturated fatty acids underlies the incorporation of ß-sheet-rich aggregates into the membranes, and that additionally induces neuronal death. This suggests a role for ferroptosis in Parkinson's disease, and highlights a new mechanism by which lipid peroxidation causes cell death.
Subject(s)
Calcium/metabolism , Ferroptosis , Iron/metabolism , Lipid Peroxidation , Parkinson Disease , alpha-Synuclein/metabolism , Cells, Cultured , Human Embryonic Stem Cells , Humans , Induced Pluripotent Stem Cells , Parkinson Disease/metabolism , Parkinson Disease/pathologyABSTRACT
Despite the wealth of genomic and transcriptomic data in Parkinson's disease (PD), the initial molecular events are unknown. Using LD score regression analysis, we show significant enrichment in PD heritability within regulatory sites for LPS-activated monocytes and that TLR4 expression is highest within human substantia nigra, the most affected brain region, suggesting a role for TLR4 inflammatory responses. We then performed extended incubation of cells with physiological concentrations of small alpha-synuclein oligomers observing the development of a TLR4-dependent sensitized inflammatory response with time, including TNF-α production. ROS and cell death in primary neuronal cultures were significantly reduced by TLR4 antagonists revealing that an indirect inflammatory mechanism involving cytokines produced by glial cells makes a major contribution to neuronal death. Prolonged exposure to low levels of alpha-synuclein oligomers sensitizes TLR4 responsiveness in astrocytes and microglial, explaining how they become pro-inflammatory, and may be an early causative event in PD.
Subject(s)
Astrocytes/metabolism , Microglia/metabolism , Parkinson Disease/metabolism , Toll-Like Receptor 4/metabolism , alpha-Synuclein/metabolism , Animals , Astrocytes/pathology , Brain/metabolism , Brain/pathology , Cell Death , Cytokines/metabolism , Humans , Inflammation/pathology , Microglia/pathology , Neurons/metabolism , Neurons/pathology , Parkinson Disease/pathology , Substantia Nigra/pathologyABSTRACT
In the original publication of this article, the author Magarida Rodrigues was written incorrectly.
ABSTRACT
Nucleotide excision repair (NER) is the primary mechanism for removal of ultraviolet light (UV)-induced DNA photoproducts and is mechanistically conserved across all kingdoms of life. Bacterial NER involves damage recognition by UvrA2 and UvrB, followed by UvrC-mediated incision either side of the lesion. Here, using a combination of in vitro and in vivo single-molecule studies we show that a UvrBC complex is capable of lesion identification in the absence of UvrA. Single-molecule analysis of eGFP-labelled UvrB and UvrC in living cells showed that UV damage caused these proteins to switch from cytoplasmic diffusion to stable complexes on DNA. Surprisingly, ectopic expression of UvrC in a uvrA deleted strain increased UV survival. These data provide evidence for a previously unrealized mechanism of survival that can occur through direct lesion recognition by a UvrBC complex.
Subject(s)
Adenosine Triphosphatases/genetics , DNA Helicases/genetics , DNA Repair , DNA, Bacterial/genetics , DNA-Binding Proteins/genetics , Endodeoxyribonucleases/genetics , Escherichia coli Proteins/genetics , Escherichia coli/radiation effects , Adenosine Triphosphatases/deficiency , Bacillus/chemistry , Bacillus/genetics , Bacillus/metabolism , DNA Damage , DNA Helicases/metabolism , DNA, Bacterial/metabolism , DNA-Binding Proteins/deficiency , Endodeoxyribonucleases/metabolism , Escherichia coli/genetics , Escherichia coli/metabolism , Escherichia coli Proteins/metabolism , Gene Deletion , Gene Expression Regulation, Bacterial , Genes, Reporter , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Microbial Viability/genetics , Microbial Viability/radiation effects , Protein Binding , Single Molecule Imaging/methods , Ultraviolet RaysABSTRACT
BACKGROUND: The aggregation of the protein É-synuclein (ÉS) underlies a range of increasingly common neurodegenerative disorders including Parkinson's disease. One widely explored therapeutic strategy for these conditions is the use of antibodies to target aggregated ÉS, although a detailed molecular-level mechanism of the action of such species remains elusive. Here, we characterize ÉS aggregation in vitro in the presence of two ÉS-specific single-domain antibodies (nanobodies), NbSyn2 and NbSyn87, which bind to the highly accessible C-terminal region of ÉS. RESULTS: We show that both nanobodies inhibit the formation of ÉS fibrils. Furthermore, using single-molecule fluorescence techniques, we demonstrate that nanobody binding promotes a rapid conformational conversion from more stable oligomers to less stable oligomers of ÉS, leading to a dramatic reduction in oligomer-induced cellular toxicity. CONCLUSIONS: The results indicate a novel mechanism by which diseases associated with protein aggregation can be inhibited, and suggest that NbSyn2 and NbSyn87 could have significant therapeutic potential.
Subject(s)
Single-Domain Antibodies/metabolism , alpha-Synuclein/metabolism , Humans , Neurodegenerative Diseases/metabolism , Neurodegenerative Diseases/physiopathology , Protein BindingABSTRACT
The protein alpha-synuclein (αS) self-assembles into toxic beta-sheet aggregates in Parkinson's disease, while it is proposed that αS forms soluble alpha-helical multimers in healthy neurons. Here, we have made αS multimers in vitro using arachidonic acid (ARA), one of the most abundant fatty acids in the brain, and characterized them by a combination of bulk experiments and single-molecule FÓ§rster resonance energy transfer (sm-FRET) measurements. The data suggest that ARA-induced oligomers are alpha-helical, resistant to fibril formation, more prone to disaggregation, enzymatic digestion and degradation by the 26S proteasome, and lead to lower neuronal damage and reduced activation of microglia compared to the oligomers formed in the absence of ARA. These multimers can be formed at physiologically-relevant concentrations, and pathological mutants of αS form less multimers than wild-type αS. Our work provides strong biophysical evidence for the formation of alpha-helical multimers of αS in the presence of a biologically relevant fatty acid, which may have a protective role with respect to the generation of beta-sheet toxic structures during αS fibrillation.
ABSTRACT
In this study we describe a new methodology to physically probe individual complexes formed between proteins and DNA. By combining nanoscale, high speed physical force measurement with sensitive fluorescence imaging we investigate the complex formed between the prokaryotic DNA repair protein UvrA2 and DNA. This approach uses a triangular, optically-trapped "nanoprobe" with a nanometer scale tip protruding from one vertex. By scanning this tip along a single DNA strand suspended between surface-bound micron-scale beads, quantum-dot tagged UvrA2 molecules bound to these '"DNA tightropes" can be mechanically interrogated. Encounters with UvrA2 led to deflections of the whole nanoprobe structure, which were converted to resistive force. A force histogram from all 144 detected interactions generated a bimodal distribution centered on 2.6 and 8.1 pN, possibly reflecting the asymmetry of UvrA2's binding to DNA. These observations successfully demonstrate the use of a highly controllable purpose-designed and built synthetic nanoprobe combined with fluorescence imaging to study protein-DNA interactions at the single molecule level.
Subject(s)
DNA Repair Enzymes/metabolism , DNA/metabolism , Nanoparticles/chemistry , Optical Tweezers , Quantum Dots/metabolism , Staining and Labeling , SolutionsABSTRACT
A powerful new approach has become much more widespread and offers insights into aspects of DNA repair unattainable with billions of molecules. Single molecule techniques can be used to image, manipulate or characterize the action of a single repair protein on a single strand of DNA. This allows search mechanisms to be probed, and the effects of force to be understood. These physical aspects can dominate a biochemical reaction, where at the ensemble level their nuances are obscured. In this paper we discuss some of the many technical advances that permit study at the single molecule level. We focus on DNA repair to which these techniques are actively being applied. DNA repair is also a process that encompasses so much of what single molecule studies benefit--searching for targets, complex formation, sequential biochemical reactions and substrate hand-off to name just a few. We discuss how single molecule biophysics is poised to transform our understanding of biological systems, in particular DNA repair.
Subject(s)
DNA Repair , Fluorescence Resonance Energy Transfer/methods , Microscopy, Atomic Force/methods , Optical Tweezers , Animals , Humans , Microscopy, Fluorescence/methodsABSTRACT
Nucleotide excision DNA repair is mechanistically conserved across all kingdoms of life. In prokaryotes, this multi-enzyme process requires six proteins: UvrA-D, DNA polymerase I and DNA ligase. To examine how UvrC locates the UvrB-DNA pre-incision complex at a site of damage, we have labeled UvrB and UvrC with different colored quantum dots and quantitatively observed their interactions with DNA tightropes under a variety of solution conditions using oblique angle fluorescence imaging. Alone, UvrC predominantly interacts statically with DNA at low salt. Surprisingly, however, UvrC and UvrB together in solution bind to form the previously unseen UvrBC complex on duplex DNA. This UvrBC complex is highly motile and engages in unbiased one-dimensional diffusion. To test whether UvrB makes direct contact with the DNA in the UvrBC-DNA complex, we investigated three UvrB mutants: Y96A, a ß-hairpin deletion and D338N. These mutants affected the motile properties of the UvrBC complex, indicating that UvrB is in intimate contact with the DNA when bound to UvrC. Given the in vivo excess of UvrB and the abundance of UvrBC in our experiments, this newly identified complex is likely to be the predominant form of UvrC in the cell.
Subject(s)
DNA Helicases/metabolism , DNA-Binding Proteins/metabolism , DNA/metabolism , Endodeoxyribonucleases/metabolism , DNA/ultrastructure , DNA Helicases/chemistry , DNA-Binding Proteins/chemistry , Diffusion , Endodeoxyribonucleases/chemistry , Microscopy, Atomic Force , Microscopy, Fluorescence , Quantum DotsABSTRACT
BACKGROUND: The objective of this study was to define the casualty rates and anatomical distribution of injuries associated with military static line parachute (MSLP) descents conducted by an Australian Army Commando Battalion. This study was conducted to identify the strategies to reduce the injury burden related to MSLP activities. METHOD: A retrospective audit of injuries resulting from MSLP descents conducted by 4th Battalion Royal Australian Regiment (4 RAR) over a 13-month period. RESULTS: A total of 554 MSLP descents over the time period were reviewed. The overall casualty rate was 5.1%. For MSLP descents onto land drop zones, the incidence of injury requiring hospital admission was 2.6%. Paratrooper bodyweight was associated with increased risk of injury (P = 0.04) and hospital admission (P = 0.003), particularly when conducting descents onto land drop zones. MSLP descents conducted onto land were associated with a higher incidence of casualties when compared with those conducted into water drop zones (P = 0.001). CONCLUSION: During the period from February 2004 until February 2005, 4 RAR (Commando) experienced higher casualty rates during MSLP descents than expected when compared with the published report. Strategies to decrease the casualty rate of MSLP descents onto land drop zones may include more extensive ground training, increased frequency of MSLP descents, use of ankle braces and the development of purpose built drop zones. Consideration should be given to establishing a maximum bodyweight threshold for the conduct of MSLP activities or acquiring parachutes with decreased descent velocity for larger paratroopers.