Filtern
Erscheinungsjahr
- 2023 (7) (entfernen)
Dokumenttyp
Sprache
- Englisch (7)
Referierte Publikation
- ja (7) (entfernen)
Schlagworte
- Affinity chromatography (2)
- Air pollution (2)
- Allergy (2)
- Nitration (2)
- Nitrogen oxides (2)
- Nitrotyrosine (2)
- Tyrosine (2)
- 6xHis (1)
- AAA (1)
- AAAA (1)
- Acute myocardial infarction (1)
- Aluminum oxide (1)
- Amino acid analysis (1)
- Aromatic amino acid analysis (1)
- Augenbohne (1)
- Bacterial lysates (1)
- Benchmarking study (1)
- Benzene-1,3,5-tricarboxylic acid (1)
- Bet v 1 (1)
- Betula pendula (1)
- Bioinformatics (1)
- Biomarker (1)
- Biosensor (1)
- Bioseparation (1)
- Birch pollen allergen (1)
- Bovine serum albumin (BSA) (1)
- Calibration (1)
- Cardiac troponin (1)
- Carrier (1)
- Carrier protein (1)
- Chemiluminescence (1)
- Combinatorial peptide library (1)
- Commercialization (1)
- Compound-independent calibration (1)
- Cytoplasm (1)
- De novo peptide sequencing (1)
- Deep learning-based tools (1)
- Diagnosis (1)
- Dimerization (1)
- Dityrosine (1)
- Dityrosine crosslinking (1)
- Downstream processing (1)
- EDTAD (1)
- Emergency (1)
- Encapsulation (1)
- Enhancement (1)
- Error correction (1)
- Escherichia coli (1)
- Ethylenediaminetetraacetic acid (1)
- Flow injection immunoassay (1)
- Grass pollen (1)
- Heart attack (1)
- Heavy chains (1)
- HexaHis-Tag (1)
- His6 (1)
- His8 (1)
- Histidine (1)
- Hydrochloric acid (1)
- IMAC purification (1)
- IgE (1)
- IgG (1)
- Immunocapture (1)
- Immunoglobulin E (1)
- Immunoglobulins (1)
- Immunometric assay (1)
- Immunometric biosensor (1)
- Immunosensor (1)
- Inflammation (1)
- Internal standard (1)
- Light chains (1)
- Luminol (1)
- Mass spectrometry (1)
- Metrology (1)
- Microfluidic system (1)
- Missing fragmentation sites (1)
- Monoclonal antibodies (1)
- Monoclonal antibody (1)
- Monolithic column (1)
- NIST (1)
- Nanocarrier (1)
- Nanoparticles (1)
- Nanoscience (1)
- Neoallergen (1)
- Neoepitopes (1)
- Nickel (1)
- Nickel chelate (1)
- Oligomerization (1)
- Online biosensor (1)
- Ozone (1)
- Peptide binder (1)
- Peroxidase (1)
- Pflanzenvirus (1)
- Phenylalanine (1)
- Phenylketonuria (1)
- Phl p 5 (1)
- Phleum pratense (1)
- Plant virus (1)
- Polishing (1)
- Preprocessing (1)
- Protein degradation (1)
- Protein hydrolysis (1)
- Protein nitration (1)
- Protein oligomers (1)
- Quantitative protein analysis (1)
- Recombinant protein (1)
- Reference material (1)
- Reference materials (1)
- Sapphire (1)
- Schlangenbohne (1)
- Sequence coverage (1)
- Sequencing algorithm (1)
- TLR4 activation (1)
- Terephthalic acid (1)
- Toll-like receptor 4 (1)
- Traceability (1)
- Tryptophan (1)
- Upscaling (1)
- Vigna unguiculata (1)
Organisationseinheit der BAM
Chemical modification by peroxynitrite enhances TLR4 activation of the grass pollen allergen Phl p 5
(2023)
The chemical modification of aeroallergens by reactive oxygen and nitrogen species (ROS/RNS) may contribute to the growing prevalence of respiratory allergies in industrialized countries. Post-translational modifications can alter the immunological properties of proteins, but the underlying mechanisms and effects are not well understood. In this study, we investigate the Toll-like receptor 4 (TLR4) activation of the major birch and grass pollen allergens Bet v 1 and Phl p 5, and how the physiological oxidant peroxynitrite (ONOO–) changes the TLR4 activation through protein nitration and the formation of protein dimers and higher oligomers. Of the two allergens, Bet v 1 exhibited no TLR4 activation, but we found TLR4 activation of Phl p 5, which increased after modification with ONOO– and may play a role in the sensitization against this grass pollen allergen. We attribute the TLR4 activation mainly to the two-domain structure of Phl p 5 which may promote TLR4 dimerization and activation. The enhanced TLR4 signaling of the modified allergen indicates that the ONOO–-induced modifications affect relevant protein-receptor interactions. This may lead to increased sensitization to the grass pollen allergen and thus contribute to the increasing prevalence of allergies in the Anthropocene, the present era of globally pervasive anthropogenic influence on the environment.
Comprehensive evaluation of peptide de novo sequencing tools for monoclonal antibody assembly
(2023)
Monoclonal antibodies are biotechnologically produced proteins with various applications in research, therapeutics and diagnostics. Their ability to recognize and bind to specific molecule structures makes them essential research tools and therapeutic agents. Sequence information of antibodies is helpful for understanding antibody–antigen interactions and ensuring their affinity and specificity. De novo protein sequencing based on mass spectrometry is a valuable method to obtain the amino acid sequence of peptides and proteins without a priori knowledge. In this study, we evaluated six recently developed de novo peptide sequencing algorithms (Novor, pNovo 3, DeepNovo, SMSNet, PointNovo and Casanovo), which were not specifically designed for antibody data. We validated their ability to identify and assemble antibody sequences on three multi-enzymatic data sets. The deep learning-based tools Casanovo and PointNovo showed an increased peptide recall across different enzymes and data sets compared with spectrum-graph-based approaches. We evaluated different error types of de novo peptide sequencing tools and their performance for different numbers of missing cleavage sites, noisy spectra and peptides of various lengths. We achieved a sequence coverage of 97.69–99.53% on the light chains of three different antibody data sets using the de Bruijn assembler ALPS and the predictions from Casanovo. However, low sequence coverage and accuracy on the heavy chains demonstrate that complete de novo protein sequencing remains a challenging issue in proteomics that requires improved de novo error correction, alternative digestion strategies and hybrid approaches such as homology search to achieve high accuracy on long protein sequences.
Protein modifications such as oligomerization and tyrosine nitration alter the immune response to allergens and may contribute to the increasing prevalence of allergic diseases. In this mini-review, we summarize and discuss relevant findings for the major birch and grass pollen allergens Bet v 1 and Phl p 5 modified with tetranitromethane (laboratory studies), peroxynitrite (physiological processes), and ozone and nitrogen dioxide environmental conditions). We focus on tyrosine nitration and the formation of protein dimers and higher oligomers via dityrosine cross-linking and the immunological effects studied.
Cardiac troponin I (cTnI) is a crucial biomarker for diagnosing cardiac vascular diseases, including acute myocardial infarction (AMI). This study presents a proof-of-concept chemiluminescence-based immunosensor for rapid and accurate measurement of cTnI, with the potential for online monitoring. The immunosensor incorporates a flow cell design and a sensitive complementary metal-oxide-semiconductor (CMOS) camera for optical readout. A microfluidic setup was established to enable selective and quasi-online determination of cTnI within ten minutes. The sensor was tested with recombinant cTnI in phosphate buffer, demonstrating measurements in the concentration range of 2–25 µg/L, with a limit of detection (LoD) of 0.6 µg/L (23 pmol/L) achieved using the optimized system. The immunosensor exhibited high selectivity, as no cross-reactivity was observed with other recombinant proteins such as cTnT and cTnC at a concentration of 16 µg/L. Measurements with diluted blood plasma and serum yielded an LoD of 60 µg/L (2.4 nmol/L) and 70 µg/L (2.9 nmol/L), respectively. This biosensor offers a promising approach for the rapid and sensitive detection of cTnI, contributing to the diagnosis and management of acute myocardial infarction and other cardiac vascular diseases.
The cowpea chlorotic mottle virus (CCMV) is a plant virus explored as a nanotechnological platform. The robust self-assembly mechanism of its capsid protein allows for drug encapsulation and targeted delivery. Additionally, the capsid nanoparticle can be used as a programmable platform to display different molecular moieties. In view of future applications, efficient production and purification of plant viruses are key steps. In established protocols, the need for ultracentrifugation is a significant limitation due to cost, difficult scalability, and safety issues. In addition, the purity of the final virus isolate often remains unclear. Here, an advanced protocol for the purification of the CCMV from infected plant tissue was developed, focusing on efficiency, economy, and final purity. The protocol involves precipitation with PEG 8000, followed by affinity extraction using a novel peptide aptamer. The efficiency of the protocol was validated using size exclusion chromatography, MALDI-TOF mass spectrometry, reversed-phase HPLC, and sandwich immunoassay. Furthermore, it was demonstrated that the final eluate of the affinity column is of exceptional purity (98.4%) determined by HPLC and detection at 220 nm. The scale-up of our proposed method seems to be straightforward, which opens the way to the large-scale production of such nanomaterials. This highly improved protocol may facilitate the use and implementation of plant viruses as nanotechnological platforms for in vitro and in vivo applications.
Immobilized metal affinity chromatography (IMAC) is a widely used technique for purifying polyhistidine-tagged recombinant proteins. However, it often has practical limitations that require complex optimizations and additional steps for purification. In this study, we introduce functionalized corundum particles as a novel, efficient, and economical method for purifying recombinant proteins in a column-free format. The corundum surface is modified with amino silane APTES, followed by EDTA dianhydride, and then loaded with nickel ions. We used the Kaiser test to monitor the modification process and ICP-MS to quantify the metal-binding capacity. To evaluate the system, we used His-tagged protein A/G (PAG) mixed with bovine serum albumin (BSA). The corundum particles exhibited a binding capacity of approximately 3 mg of protein per gram of corundum or 2.4 mg per 1 mL of corundum suspension. We also examined cytoplasm obtained from different E. coli strains as an example of a complex matrix. Varying the imidazole concentration in the loading and washing buffers showed that higher concentrations during loading improved purity. Even with sample volumes as large as one liter, we successfully isolated recombinant proteins down to a concentration of 1 µg/mL. We found higher purity levels with corundum when comparing the corundum material to standard Ni–NTA agarose beads. We successfully purified His6-MBP-mSA2, a fusion protein comprising monomeric streptavidin and maltose-binding protein, from E. coli cytoplasm, demonstrating the method's applicability. We also purified SARS-CoV-2-S-RBD-His8 expressed in human Expi293F cells, confirming its suitability for mammalian cell culture supernatants. The material cost of the nickel-loaded corundum material (without regeneration) is estimated to be less than 30 cents per gram of functionalized support or 10 cents per milligram of isolated protein. Another advantage of this system is the exceptional physical and chemical stability of corundum particles. Overall, we have demonstrated that this novel material offers an efficient, robust, and cost-effective purification platform for His-tagged proteins, even in challenging, complex matrices and large sample volumes with low product concentrations. This method has potential applications in both small laboratories and large-scale industrial settings.
Quantitative 1H nuclear magnetic resonance (qNMR) of aromatic amino acids for protein quantification
(2023)
Hydrolysis of protein samples into amino acids facilitates the use of NMR spectroscopy for protein and peptide quantification. Different conditions have been tested for quantifying aromatic amino acids and proteins. The pH-dependent signal shifts in the aromatic region of amino acid samples were examined. A pH of 12 was found to minimize signal overlap of the four aromatic amino acids. Several aromatic compounds, such as terephthalic acid, sulfoisophthalic acid, and benzene tricarboxylic acid, were applied as internal standards. The quantification of amino acids from an amino acid standard was performed. Using the first two suggested internal standards, recovery was ~97% for histidine, phenylalanine, and tyrosine at a concentration of approximately 1 mM in solution. Acidic hydrolysis of a certified reference material (CRM) of bovine serum albumin (BSA) and subsequent quantification of Phe and Tyr yielded recoveries of 98% ± 2% and 88% ± 4%, respectively, at a protein concentration of 16 g/L or 250 µM.