Aequorin
Luminescent Measurements
Mitochondrial depolarization accompanies cytochrome c release during apoptosis in PC6 cells. (1/8843)
Cytochrome c is released from mitochondria into the cytosol in cells undergoing apoptosis. The temporal relationship between cytochrome c release and loss of mitochondrial membrane potential was monitored by laser-scanning confocal microscopy in single living pheochromocytoma-6 cells undergoing apoptosis induced by staurosporine. Mitochondrial membrane potential monitored by tetramethylrhodamine methyl ester decreased abruptly in individual cells from 2 to 7 h after treatment with staurosporine. Depolarization was accompanied by cytochrome c release documented by release of transfected green fluorescent protein-tagged cytochrome c in these cells. The results show that mitochondrial depolarization accompanies cytochrome c release in pheochromocytoma-6 cells undergoing apoptosis. (+info)The dually acylated NH2-terminal domain of gi1alpha is sufficient to target a green fluorescent protein reporter to caveolin-enriched plasma membrane domains. Palmitoylation of caveolin-1 is required for the recognition of dually acylated g-protein alpha subunits in vivo. (2/8843)
Here we investigate the molecular mechanisms that govern the targeting of G-protein alpha subunits to the plasma membrane. For this purpose, we used Gi1alpha as a model dually acylated G-protein. We fused full-length Gi1alpha or its extreme NH2-terminal domain (residues 1-32 or 1-122) to green fluorescent protein (GFP) and analyzed the subcellular localization of these fusion proteins. We show that the first 32 amino acids of Gi1alpha are sufficient to target GFP to caveolin-enriched domains of the plasma membrane in vivo, as demonstrated by co-fractionation and co-immunoprecipitation with caveolin-1. Interestingly, when dual acylation of this 32-amino acid domain was blocked by specific point mutations (G2A or C3S), the resulting GFP fusion proteins were localized to the cytoplasm and excluded from caveolin-rich regions. The myristoylated but nonpalmitoylated (C3S) chimera only partially partitioned into caveolin-containing fractions. However, both nonacylated GFP fusions (G2A and C3S) no longer co-immunoprecipitated with caveolin-1. Taken together, these results indicate that lipid modification of the NH2-terminal of Gi1alpha is essential for targeting to its correct destination and interaction with caveolin-1. Also, a caveolin-1 mutant lacking all three palmitoylation sites (C133S, C143S, and C156S) was unable to co-immunoprecipitate these dually acylated GFP-G-protein fusions. Thus, dual acylation of the NH2-terminal domain of Gi1alpha and palmitoylation of caveolin-1 are both required to stabilize and perhaps regulate this reciprocal interaction at the plasma membrane in vivo. Our results provide the first demonstration of a functional role for caveolin-1 palmitoylation in its interaction with signaling molecules. (+info)Properties of filament-bound myosin light chain kinase. (3/8843)
Myosin light chain kinase binds to actin-containing filaments from cells with a greater affinity than to F-actin. However, it is not known if this binding in cells is regulated by Ca2+/calmodulin as it is with F-actin. Therefore, the binding properties of the kinase to stress fibers were examined in smooth muscle-derived A7r5 cells. Full-length myosin light chain kinase or a truncation mutant lacking residues 2-142 was expressed as chimeras containing green fluorescent protein at the C terminus. In intact cells, the full-length kinase bound to stress fibers, whereas the truncated kinase showed diffuse fluorescence in the cytoplasm. After permeabilization with saponin, the fluorescence from the truncated kinase disappeared, whereas the fluorescence of the full-length kinase was retained on stress fibers. Measurements of fluorescence intensities and fluorescence recovery after photobleaching of the full-length myosin light chain kinase in saponin-permeable cells showed that Ca2+/calmodulin did not dissociate the kinase from these filaments. However, the filament-bound kinase was sufficient for Ca2+-dependent phosphorylation of myosin regulatory light chain and contraction of stress fibers. Thus, dissociation of myosin light chain kinase from actin-containing thin filaments is not necessary for phosphorylation of myosin light chain in thick filaments. We note that the distance between the N terminus and the catalytic core of the kinase is sufficient to span the distance between thin and thick filaments. (+info)A fluorescent orthotopic bone metastasis model of human prostate cancer. (4/8843)
Here, we report a fluorescent spontaneous bone metastatic model of human prostate cancer developed by surgical orthotopic implantation of green fluorescent protein (GFP)-expressing prostate cancer tissue. Human prostate cancer PC-3 cells were transduced with the pLEIN expression retroviral vector containing the enhanced GFP and neomycin resistance genes. Stable GFP high-expression PC-3 clones were selected in vitro with G418, which were then combined and injected s.c. in nude mice. For metastasis studies, fragments of a single highly fluorescent s.c. growing tumor were implanted by surgical orthotopic implantation in the prostate of a series of nude mice. Subsequent micrometastases and metastases were visualized by GFP fluorescence throughout the skeleton, including the skull, rib, pelvis, femur, and tibia The central nervous system, including the brain and spinal cord, was also involved with tumor, as visualized by GFP fluorescence. Systemic organs, including the lung, plural membrane, liver, kidney, and adrenal gland, also had fluorescent metastases. The metastasis pattern in this model reflects the bone and other metastatic sites of human prostate cancer. Thus, this model should be very useful for the study and development of treatment for metastatic androgen-independent prostate cancer. (+info)Role of cytokine signaling molecules in erythroid differentiation of mouse fetal liver hematopoietic cells: functional analysis of signaling molecules by retrovirus-mediated expression. (5/8843)
Erythropoietin (EPO) and its cell surface receptor (EPOR) play a central role in proliferation, differentiation, and survival of erythroid progenitors. Signals induced by EPO have been studied extensively by using erythroid as well as nonerythroid cell lines, and various controversial results have been reported as to the role of signaling molecules in erythroid differentiation. Here we describe a novel approach to analyze the EPO signaling by using primary mouse fetal liver hematopoietic cells to avoid possible artifacts due to established cell lines. Our strategy is based on high-titer retrovirus vectors with a bicistronic expression system consisting of an internal ribosome entry site (IRES) and green fluorescent protein (GFP). By placing the cDNA for a signaling molecule in front of IRES-GFP, virus-infected cells can be viably sorted by fluorescence-activated cell sorter, and the effect of expression of the signaling molecule can be assessed. By using this system, expression of cell-survival genes such as Bcl-2 and Bcl-XL was found to enhance erythroid colony formation from colony-forming unit-erythroid (CFU-E) in response to EPO. However, their expression was not sufficient for erythroid colony formation from CFU-E alone, indicating that EPO induces signals for erythroid differentiation. To examine the role of EPOR tyrosine residues in erythroid differentiation, we introduced a chimeric EGFR-EPOR receptor, which has the extracellular domain of the EGF receptor and the intracellular domain of the EPOR, as well as a mutant EGFR-EPOR in which all the cytoplasmic tyrosine residues are replaced with phenylalanine, and found that tyrosine residues of EPOR are essential for erythroid colony formation from CFU-E. We further analyzed the function of the downstream signaling molecules by expressing modified signaling molecules and found that both JAK2/STAT5 and Ras, two major signaling pathways activated by EPOR, are involved in full erythroid differentiation. (+info)Nuclear translocation of green fluorescent protein-nuclear factor kappaB with a distinct lag time in living cells. (6/8843)
A highly fluorescent mutant form of the green fluorescent protein (GFP) has been fused to the human nuclear factor kappaB (NF-kappaB) p50 and p105 (p50/IkappaB gamma), a precursor protein of NF-kappaB p50. GFP-p50 and GFP-p105 were expressed in monkey COS-7 cells and human HeLa cells. Translocation of these chimeric proteins was observed by confocal laser scanning microscopy. GFP-p50 (without IkappaB gamma) in the transfected cells resided in the nucleus. On the other hand, GFP-p105 (GFP-p50 with IkappaB gamma) localized only in the cytoplasm before stimulation and translocated to the nucleus with stimulant specificity similar to that of native NF-kappaB/IkappaB. In addition, the translocation of NF-kappaB to the nucleus had a distinct lag time (a quiescent time) in the target cells. The lag time lasted 10-20 min after stimulation with hydrogen peroxide or tumor necrosis factor alpha. It was suggested that this might be due to the existence of a limiting step where NF-kappaB is released from NF-kappaB/IkappaB by the proteasome. (+info)Microtubule-dependent plus- and minus end-directed motilities are competing processes for nuclear targeting of adenovirus. (7/8843)
Adenovirus (Ad) enters target cells by receptor-mediated endocytosis, escapes to the cytosol, and then delivers its DNA genome into the nucleus. Here we analyzed the trafficking of fluorophore-tagged viruses in HeLa and TC7 cells by time-lapse microscopy. Our results show that native or taxol-stabilized microtubules (MTs) support alternating minus- and plus end-directed movements of cytosolic virus with elementary speeds up to 2.6 micrometer/s. No directed movement was observed in nocodazole-treated cells. Switching between plus- and minus end-directed elementary speeds at frequencies up to 1 Hz was observed in the periphery and near the MT organizing center (MTOC) after recovery from nocodazole treatment. MT-dependent motilities allowed virus accumulation near the MTOC at population speeds of 1-10 micrometer/min, depending on the cell type. Overexpression of p50/dynamitin, which is known to affect dynein-dependent minus end-directed vesicular transport, significantly reduced the extent and the frequency of minus end-directed migration of cytosolic virus, and increased the frequency, but not the extent of plus end-directed motility. The data imply that a single cytosolic Ad particle engages with two types of MT-dependent motor activities, the minus end- directed cytoplasmic dynein and an unknown plus end- directed activity. (+info)Estimation of the number of alpha-helical and beta-strand segments in proteins using circular dichroism spectroscopy. (8/8843)
A simple approach to estimate the number of alpha-helical and beta-strand segments from protein circular dichroism spectra is described. The alpha-helix and beta-sheet conformations in globular protein structures, assigned by DSSP and STRIDE algorithms, were divided into regular and distorted fractions by considering a certain number of terminal residues in a given alpha-helix or beta-strand segment to be distorted. The resulting secondary structure fractions for 29 reference proteins were used in the analyses of circular dichroism spectra by the SELCON method. From the performance indices of the analyses, we determined that, on an average, four residues per alpha-helix and two residues per beta-strand may be considered distorted in proteins. The number of alpha-helical and beta-strand segments and their average length in a given protein were estimated from the fraction of distorted alpha-helix and beta-strand conformations determined from the analysis of circular dichroism spectra. The statistical test for the reference protein set shows the high reliability of such a classification of protein secondary structure. The method was used to analyze the circular dichroism spectra of four additional proteins and the predicted structural characteristics agree with the crystal structure data. (+info)Aequorin is a bioluminescent protein found in certain jellyfish species, such as Aequorea victoria. It emits light when it undergoes a conformational change in the presence of calcium ions (Ca^2+^). This property makes aequorin a valuable tool in studying intracellular calcium levels and dynamics in various biological systems, including cells and model organisms.
The reaction that leads to light emission involves the binding of Ca^2+^ ions to aequorin, which then triggers the oxidation of coelenterazine, a chromophore molecule, to produce coelenteramide along with the release of energy in the form of blue light (approximately 469 nm). The intensity of the light emitted is directly proportional to the concentration of Ca^2+^ ions, allowing researchers to monitor and measure calcium levels in real-time.
Aequorin has been widely used in various research fields, such as neuroscience, cardiology, and cell biology, to investigate calcium signaling pathways and their roles in numerous physiological processes and diseases. Additionally, aequorin-based biosensors have been developed to study calcium dynamics in vivo, providing valuable insights into the complex interplay between calcium homeostasis and cellular functions.
Luminescent measurements refer to the quantitative assessment of the emission of light from a substance that has been excited, typically through some form of energy input such as electrical energy or radiation. In the context of medical diagnostics and research, luminescent measurements can be used in various applications, including bioluminescence imaging, which is used to study biological processes at the cellular and molecular level.
Bioluminescence occurs when a chemical reaction produces light within a living organism, often through the action of enzymes such as luciferase. By introducing a luciferase gene into cells or organisms, researchers can use bioluminescent measurements to track cellular processes and monitor gene expression in real time.
Luminescent measurements may also be used in medical research to study the properties of materials used in medical devices, such as LEDs or optical fibers, or to develop new diagnostic tools based on light-emitting nanoparticles or other luminescent materials.
In summary, luminescent measurements are a valuable tool in medical research and diagnostics, providing a non-invasive way to study biological processes and develop new technologies for disease detection and treatment.
Luminescent proteins are a type of protein that emit light through a chemical reaction, rather than by absorbing and re-emitting light like fluorescent proteins. This process is called bioluminescence. The light emitted by luminescent proteins is often used in scientific research as a way to visualize and track biological processes within cells and organisms.
One of the most well-known luminescent proteins is Green Fluorescent Protein (GFP), which was originally isolated from jellyfish. However, GFP is actually a fluorescent protein, not a luminescent one. A true example of a luminescent protein is the enzyme luciferase, which is found in fireflies and other bioluminescent organisms. When luciferase reacts with its substrate, luciferin, it produces light through a process called oxidation.
Luminescent proteins have many applications in research, including as reporters for gene expression, as markers for protein-protein interactions, and as tools for studying the dynamics of cellular processes. They are also used in medical imaging and diagnostics, as well as in the development of new therapies.
COVID-19 testing
Marc Zimmer
Nanomedicine
Lanthanide probes
Protein tag
Stern-Volmer relationship
Aequorin
Outline of photography
Thalappil Pradeep
Renilla-luciferin 2-monooxygenase
Tetrasodium tris(bathophenanthroline disulfonate)ruthenium(II)
Lactoferrin
Fluorescence in the life sciences
Reporter gene
Green fluorescent protein
Lomonosov Gold Medal
Amyloid plaques
Pseudotyping
Calmodulin
Photoprotein
Antibiotic sensitivity testing
Anthony Campbell (British biochemist)
Coelenterazine
Gerd Ulrich Nienhaus
Bioluminescence imaging
Cuttlefish
Streptavidin
Apoptosis
Eos (protein)
Biofilm
Tau Protein Binding Modes in Alzheimer's Disease for Cationic Luminescent Ligands - SeRC
A High-Resolution Luminescent Assay for Rapid and Continuous Monitoring of Protein Translocation across Biological Membranes<...
Fluorescent Markers: Proteins and Nanocrystals | IntechOpen
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector
Use of Resonance Energy Transfer Techniques for In Vivo Detection of Chemokine Receptor Oligomerization
RCSB PDB - 3DPZ: Structure of the Yellow Fluorescent Protein Citrine Frozen at 4000 Atmospheres Number 3: Structure 25 in a...
COVID-19 testing - Wikipedia
Accepted Publication:Internalization of a preformed atomically precise silver cluster in proteins by multistep events and...
Manganese could make luminescent materials and the conversion of sunlight more sustainable
Results for 'Cell Metabolism Kits' | Abcam: antibodies, proteins, kits...
Positioning of nucleosomes containing γ-H2AX precedes active DNA demethylation and transcription initiation | Nature...
Dimeric binding of plant alkaloid ellipticine to human serum proteins - JASCO
Submillisecond protein folding kinetics studied by ultrarapid mixing - JASCO
IJMS | Free Full-Text | The Effect of Silica Nanoparticles (SiNPs) on Cytotoxicity, Induction of Oxidative Stress and Apoptosis...
Luciferases | Harvard Catalyst Profiles | Harvard Catalyst
NHANES 2001-2002: C-Reactive protein (CRP), Fibrinogen, Bone Alkaline Phosphatase & Urinary N-telopeptides Data...
Inhibition of the foot-and-mouth disease virus subgenomic replicon by RNA aptamers. - White Rose Research Online
PRKCI protein kinase C iota [Homo sapiens (human)] - Gene - NCBI
Publications | Max Planck Institute of Biochemistry
NIOSHTIC-2 Search Results - Basic View
DayGlo Science | The Scientist Magazine®
Alice Ting's Profile | Stanford Profiles
HSP90β regulates EAAT2 expression and participates in ischemia‑reperfusion injury in rats
Co-expression of Multiple Chimeric Fluorescent Fusion Proteins in an Efficient Way in Plants | Protocol
The cyclophilin-like domain of Ran-binding protein-2 modulates selectively the activity of the ubiquitin-proteasome system and...
The epichaperome is a mediator of toxic hippocampal stress and leads to protein connectivity-based dysfunction | Nature...
Understanding Luminescent Reporter Assay Design
KAKEN - Research Projects | Development of chemical methods for analyzing protein molecules function in their natural habitat ...
A genetically engineered Plasmodium falciparum expressing NanoLuc as an innovative tool for malaria drug discovery.|Nagasaki...
Types of luminescent2
- For the first time, Manganese complexes show the types of luminescent properties and photocatalytic behavior that were primarily associated with noble metal compounds until now. (phys.org)
- In this thesis, we applied the 2D POLIM technique to investigate the fundamental optoelectronic process in different types of luminescent materials. (lu.se)
Genetic2
- These vectors are designed for protein transient expression and genetic transformation. (jove.com)
- Most cases of human prion disease are apparently spontaneously occurring (sporadic CJD [sCJD]) or are associated with mutations in the human prion protein gene, designated PRNP (genetic CJD, Gerstmann-Sträussler-Scheinker disease, or fatal familial insomnia). (cdc.gov)
Fluorescence2
- The ligand bTVBT4 shows specificity for detection of tau proteins in the Alzheimer's fold by means of fluorescence imaging. (e-science.se)
- Our extensive SpectraMax® line of user-friendly microplate readers - the industry's most cited brand - provide great flexibility for labs conducting applications ranging from ELISAs to nucleic acid and protein quantitation and include absorbance, fluorescence, and luminescence. (moleculardevices.com)
Assay2
- To demonstrate its versatility, we implemented and validated the assay in vitro and in vivo for the bacterial Sec system and the mitochondrial protein import apparatus. (uni-luebeck.de)
- We used a rapid molecular conversion assay (protein misfolding cyclic amplification) to test whether brain homogenates from specimens of classical bovine spongiform encephalopathy (BSE), atypical BSE (H-type BSE and L-type BSE), classical scrapie, atypical scrapie, and chronic wasting disease can convert normal human prion protein to the abnormal disease-associated form. (cdc.gov)
Bacteria2
- Structure of lumazine protein, an optical transponder of luminescent bacteria. (mpg.de)
- E. coli already has a sensor to detect TNT, which it can metabolize and use as fuel, but the university lab was able to change the nature of the bacterium "so instead of having the bacteria just break down TNT, it activates a luminescent protein" that was derived from a different organism, he said. (nationaldefensemagazine.org)
LUMINESCENCE1
- While luminescence has become more established in biological research, the green fluorescent protein (GFP) behind the glow was first identified in Aequorea victoria . (buzzfeednews.com)
Genes1
- Although HMG proteins do not possess intrinsic transcriptional activity, they are called architectural transcription factors because they modulate the transcription of their target genes by altering the chromatin structure at the promoter and/or enhancers 15 . (nature.com)
Biological4
- Therefore, this chapter will show exciting results of the group using fluorescent proteins and nanocrystals in biological systems. (intechopen.com)
- After publishing Aglow in the Dark in 2005, Gruber moved to Brown University for postdoctoral study on ways to use fluorescent proteins as biological sensors. (the-scientist.com)
- Protein is one of the central biomolecules that is involved in almost all biological events and thus its quantitative analysis has been actively conducted for many years. (nii.ac.jp)
- 2D POLIM was also applied to explore the aggregation state of proteins in the biological system. (lu.se)
Specificity1
- Fluorescent reporter proteins in the Drosophila model system offer a degree of specificity that allows monitoring cellular and biochemical phenomena in vivo, such as autophagy, mitophagy, and changes in the redox state of cells. (intechopen.com)
Inhibitors1
- After transfecting for 24 hr, cells were lysed by RIPA buffer including protease inhibitors, and biotinylated proteins were pulled down with streptavidin beads. (elifesciences.org)
Fluorescent protein4
- An HIV vector containing a gene encoding the green fluorescent protein (GFP) was injected into the subretinal space of rat eyes. (nih.gov)
- Few scientists knew the complete history of fluorescent protein research, so he and Pieribone wrote a book about it. (the-scientist.com)
- This study shows the CLD of RanBP2 promotes selectively the accumulation of a subset of reporter substrates of the UPS, such as the ubiquitin (Ub)-fusion yellow fluorescent protein (YFP) degradation substrate, Ub(G76V)-YFP, and the N-end rule substrate, Ub-R-YFP. (duke.edu)
- In this study, we genetically modified P. falciparum to simultaneously express GFP, a fluorescent protein, and NanoLuc, a luciferase. (nagasaki-u.ac.jp)
Luciferase2
- To address this, we applied NanoLuc split-luciferase to produce a new strategy for measuring protein transport. (uni-luebeck.de)
- Cloning and characterization of an active fragment of luciferase from a luminescent marine alga, Pyrocystis lunula. (bio.net)
Kinase3
- We have previously shown that HMGA2-induced transcription requires phosphorylation of H2A.X at S139, which in turn is mediated by the protein kinase ataxia telangiectasia mutated (ATM) 10 . (nature.com)
- This gene encodes a member of the protein kinase C (PKC) family of serine/threonine protein kinases. (nih.gov)
- This protein kinase is calcium-independent and phospholipid-dependent. (nih.gov)
Antibodies1
- Abcam: antibodies, proteins, kits. (abcam.com)
Reporter4
- This book chapter will comment on fluorescent reporter proteins and nanocrystals' applicability as fluorescent markers. (intechopen.com)
- This transgenic P. falciparum reporter line constantly expresses two reporter proteins, GFP and NanoLuc, at high levels in two different hosts, human and mosquito. (nagasaki-u.ac.jp)
- By utilising the expression of these two reporter proteins, P. falciparum can be successfully visualised and quantified with high sensitivity. (nagasaki-u.ac.jp)
- We have created a transgenic P. falciparum that expresses two reporter proteins, GFP and NanoLuc, at high levels in both the human- and the vector mosquito stage. (nagasaki-u.ac.jp)
Transgenic1
- Objective 4 is to develop transgenic lines expressing fluorescent and luminescent reporters for high-throughput screening of candidate treatments. (usda.gov)
Markers1
- Highly luminescent QDs could serve as luminescent markers, while magnetic nanoparticles could be easily manipulated under the external magnetic field. (springer.com)
Magnetic1
- Multiplexed immunoassays for proteins using magnetic luminescent nanoparticles for internal calibration. (cdc.gov)
Molecules1
- In this research project, we successfully developed several original methods (or synthetic small molecules) based on chemistry that allow for selective labeling and imaging target proteins under nearly natural conditions. (nii.ac.jp)
Pathologic1
- The fundamental event in prion disease pathogenesis is thought to be the seeded conversion of normal prion protein to its pathologic isoform. (cdc.gov)
Aggregation1
- Design of anti- and pro-aggregation variants to assess the effects of methionine oxidation in human prion protein. (mpg.de)
Cells10
- In future research projects, Wenger and his group want to improve the luminescent properties of the new manganese complexes and anchor them on suitable semiconductor materials for use in solar cells. (phys.org)
- Researchers can introduce these glowing proteins into cells to track all kinds of activity, including the growth of tumors or chatter between nerve cells. (the-scientist.com)
- Heat shock protein (HSP) 90 is abundant in cells, mainly in the form of homodimers, including HSP90α and HSP90β. (spandidos-publications.com)
- As a molecular chaperone, HSP90 regulates the conformational maturation and functional stability of many signaling proteins in cells, serves important roles in cell growth, differentiation, apoptosis and tumor development and is an important antitumor target ( 8 , 9 ). (spandidos-publications.com)
- These methods may contribute to analyzing protein structure and functions in living cells. (nii.ac.jp)
- En face co-immunostaining of the mouse aortic arch revealed a low level of PDCD4 in endothelial cells undergoing pulsatile shear stress. (plos.org)
- Application of unidirectional pulsatile shear stress to human umbilical vein endothelial cells (HUVECs) decreased PDCD4 protein but not mRNA level. (plos.org)
- This made the cells luminescent, making them easier to track. (futurity.org)
- [2] [3] The cells within the biofilm produce the EPS components, which are typically a polymeric conglomeration of extracellular polysaccharides , proteins , lipids and DNA . (wikipedia.org)
- In conclusion, we showed a multilayered role of DC subsets in priming Tfh cells in protein immunization, and we unveiled the importance of G-CSFR signaling in the development and function pDCs. (bvsalud.org)
Researchers3
- University of Basel researchers have reached an important milestone in their quest to produce more sustainable luminescent materials and catalysts for converting sunlight into other forms of energy. (phys.org)
- Our microplate readers and software are the industry's most cited and have empowered life science researchers to advance protein and cell biology. (moleculardevices.com)
- The researchers created a tightly knit 3D mesh in a hydrogel containing water, hyaluronic acid and short protein sequences associated with brown-fat growth and function. (futurity.org)
Protease1
- Interplay of PDZ and protease domain of DegP ensures efficient elimination of misfolded proteins. (mpg.de)
Complexes1
- Now, a team led by Professor Oliver Wenger and his doctoral student Patrick Herr from the University of Basel have for the first time succeeded in producing luminescent manganese complexes in which exposure to light causes the same reactions to take place as in ruthenium or iridium compounds. (phys.org)
Aequorin1
- After tediously extracting thousands of specimens to identify the luminescent components back in the 1960s, a scientist named Osamu Shimomura isolated GFP and aequorin, another light-emitting protein, which led to a 2008 Nobel Prize in chemistry. (buzzfeednews.com)
Expression11
- The present study aimed to investigate the effects of changes in heat shock protein (HSP)90β expression and verify whether HSP90β regulates EAAT2 expression in a cerebral ischemia‑reperfusion injury model. (spandidos-publications.com)
- It takes advantage of using a single expression plasmid that contains multiple functionally independent protein expressing cassettes to achieve protein co-expression. (jove.com)
- The main advantage of this technique is the high efficiency of co-expressing cellular fusion proteins in one expression vector. (jove.com)
- Amplify DNA fragments that are necessary for the construction of the semi-independent protein expression cassettes by standard PCR reactions with their corresponding primers and high-fidelity polymerase. (jove.com)
- Mix the DNA fragments designed for the same protein expression cassette together in one PCR tube to a final volume of five microliters. (jove.com)
- Amplify the entire semi-independent protein expression cassette by a second round of PCR. (jove.com)
- Next, linearize the final protein expression backbone vector POC 18, and vector CAMBIA 1300, by adding four units of small one into a final 10 microliter reaction volume. (jove.com)
- HSP90 inhibition may also enhance synaptic protein expression via activation of heat shock factor 1 (HSF-1) transcriptional regulation 16 . (nature.com)
- This is accomplished by increasing both the interaction strength and number of interactions among participant proteins, which is not necessarily accompanied by a change in expression levels. (nature.com)
- As a control, the expression levels of enzyme-fused protein and target proteins were detected using each protein-specific antibody (left panel). (elifesciences.org)
- Programmable DNA binding proteins have emerged as an exciting platform for engineering synthetic transcription factors for modulating endogenous gene expression 5 - 11 . (cdc.gov)
Cellular2
- At the sub-cellular scale, maps document the spatial organization of proteins, RNA, DNA, and metabolites with nanometer precision and temporal acuity on the order of seconds. (stanford.edu)
- The prion hypothesis posits that the posttranslational conformational conversion of a host's normal cellular prion protein (PrP C ) by the abnormal form of the prion protein (PrP Sc ) is the fundamental event in prion disease pathogenesis and that PrP Sc itself constitutes the infectious agent. (cdc.gov)
Interactions1
- 2014. Fringe proteins modulate Notch-ligand cis and trans interactions to specifysignaling states. (invivogen.com)
Abundant1
- In addition to nucleosomes, chromatin contains non-histone chromatin-associated proteins, of which the high-mobility group proteins are the most abundant. (nature.com)
Heat shock p1
- Pertinent to AD pathophysiology, heat shock protein 90 (HSP90)/co-chaperone complex folds tau or hyperphosphorylated tau, whereas heat shock protein 70-carboxyl-terminus of HSP70 Interacting protein (HSP70-CHIP) complex mediates degradation 13 , 14 . (nature.com)
Translocation3
- Protein translocation is a fundamental process in biology. (uni-luebeck.de)
- Overall, this technology represents a major step forward, providing a powerful new tool for fundamental mechanistic enquiry of protein translocation and for inhibitor (drug) screening, with an intensity and rigor unattainable through classical methods. (uni-luebeck.de)
- Active DNA demethylation also requires GADD45A (growth arrest and DNA damage protein 45 alpha) and TET1 (ten-eleven translocation methylcytosine dioxygenase 1), which sequentially oxidize 5-methylcytosine (5mC) to 5-carboxylcytosine (5caC) 18 , 19 and are cleared through DNA repair mechanisms. (nature.com)
Transcription4
- However, the order of events and the precise function of high-mobility group proteins during transcription initiation remain unclear. (nature.com)
- Here we show that high-mobility group AT-hook 2 protein (HMGA2) induces DNA nicks at the transcription start site, which are required by the histone chaperone FACT complex to incorporate nucleosomes containing the histone variant H2A.X. Further, phosphorylation of H2A.X at S139 (γ-H2AX) is required for repair-mediated DNA demethylation and transcription activation. (nature.com)
- Among the established custom DNA binding domains, Cas9 is most easily scaled to facilitate genome-scale perturbations 3 , 4 due to its simplicity of programming relative to zinc finger proteins and transcription activator-like effectors (TALEs). (cdc.gov)
- Cas9 nuclease can be converted into an RNA-guided DNA binding protein (dCas9) via inactivation of its two catalytic domains 12 , 13 and then fused to transcription activation domains. (cdc.gov)
Structure2
- 1-- including one high-quality, chromosome-level reference genome assembly using state-of-the-art long-read sequencing technology-- to quantify geographic differences, infer patterns and timing of parasite spread, and identify gene-specific selection, gene function, and structure of essential proteins. (usda.gov)
- Marie Skepö (PI), has in collaboration with Lise Arleth and Kresten Lindorff-Larsen at University of Copenhagen, and Jens Preben Morth at University of Oslo, been awarded 6.8 MNOK for studying the structure of membrane proteins. (lu.se)
Explore1
- Current technical limitations curb our ability to explore global changes in protein level connectivity, restricting how to translate key network changes into AD therapies. (nature.com)
Detection2
- Luminescent conjugated oilgothiphenes are developed for early-stage detection of Alzheimer's disease. (e-science.se)
- Detection of the virus is usually done either by looking for the virus's inner RNA, or pieces of protein on the outside of the virus. (wikipedia.org)
Degradation2
Inhibits1
- Blasticidin is a peptidyl nucleoside antibiotic isolated from Streptomyces griseochromogenes that inhibits protein synthesis by interfering with the peptide-bond formation in the ribosomal machinery. (invivogen.com)
Sensors1
- A bacterium like E. coli is "essentially a very simple cell," with built-in protein sensors to perform its natural functions, Enzymit CEO Gideon Lapidoth said in an interview. (nationaldefensemagazine.org)
Perturbations2
Regulates1
- Protein phosphorylation regulates actomyosin-driven vesicle movement in cell extracts isolated from the green algae, Chara corallina. (bio.net)
Mediates1
- Here we will focus on HMG AT-hook 2 protein (HMGA2), a member of the HMGA family that mediates transforming growth factor beta 1 (TGFB1, commonly known as TGFβ1) signaling 16 . (nature.com)
Cell biology1
- This method can help answer key questions in the plant molecular and cell biology field such as, how can we proteins in the cell. (jove.com)
Function2
- This protein is therefore highly sensitive to subangstrom deformations and its function must be understood at the subangstrom level. (rcsb.org)
- These results have significant implications for protein function prediction and biomolecule design and engineering, because they suggest methods to tune protein function by modification of the protein scaffold. (rcsb.org)
Light2
- Made possible by the same luminescent proteins that light up jellyfish, a synthesized version is applied to the ice cream to give it its glow. (foodiggity.com)
- Proteins which are involved in the phenomenon of light emission in living systems. (bvsalud.org)
Tissues1
- 0.05) expressed in the cerebellar cortex, piriform lobe, medulla, and corpus callosum of the adult yak while in the young yak brain tissues, the protein expressions were significantly found in the white matter of the cerebellum, pineal gland, corpus callosum, and cerebellar cortex. (scielo.br)
Backbone1
- These structures provide the backbone upon which proteome-wide connectivity, and in turn, protein networks become disturbed and ultimately dysfunctional. (nature.com)
Occurs1
- It is conclusively shown that the ligand-protein binding occurs at the hydrophobic pocket defined by residues Ile360, Thr361, and His362. (e-science.se)
Properties1
- Knowledge of the properties of proteins right down to atomic level is essential for making it easier and faster for the pharmaceutical industry to manufacture protein-based drugs in liquid form. (lu.se)
Human2
Target1
- Specifically, the PDCD4 protein combines directly with the mRNA coding region of the target gene ( MYB/c-MYB ) to block translation [2] . (plos.org)
Specifically1
- The cyclophilin-like domain (CLD) of Ran-binding protein-2 (RanBP2/Nup358) associates specifically with at least one subunit, S1, of the base subcomplex of the 19S RP, but the functional implications of this interaction on the UPS activity are elusive. (duke.edu)
Term1
- We introduce the term protein connectivity-based dysfunction (PCBD) to define this mechanism. (nature.com)
Methods1
- We have developed a novel method for co-expressing multiple chimeric fluorescent fusion proteins in plants to overcome the difficulties of conventional methods. (jove.com)