The mapping of linear B-cell epitope regions in desmoglein 1 and 3
... similarity to the native antigen which allows the binding of antibodies. This is a rapid, practical, and cost-effective method for linear epitope region identification [20, 21]. B-cell epitope mapping using a series of pin-attached overlapping synthetic peptides can be a very efficient way to identi ...
... similarity to the native antigen which allows the binding of antibodies. This is a rapid, practical, and cost-effective method for linear epitope region identification [20, 21]. B-cell epitope mapping using a series of pin-attached overlapping synthetic peptides can be a very efficient way to identi ...
cDNA, genomic sequence cloning and overexpression of ribosomal
... The ribosomal protein L9 (RPL9), a component of the 60S subunit, encoded by the rpL9 gene, belongs to the L6P family of ribosomal proteins. Within the context of the ribosome, the L9 protein is located in the large subunit, near proteins L1, L2, L16, L19, and L28 (Walleczek et al., 1989; Brimacombe ...
... The ribosomal protein L9 (RPL9), a component of the 60S subunit, encoded by the rpL9 gene, belongs to the L6P family of ribosomal proteins. Within the context of the ribosome, the L9 protein is located in the large subunit, near proteins L1, L2, L16, L19, and L28 (Walleczek et al., 1989; Brimacombe ...
Does Plant Cell Death Induced by Ptr ToxA Require Toxin Entry?
... RGD cell attachment site within additional essential amino acids CKII phosphorylation site ...
... RGD cell attachment site within additional essential amino acids CKII phosphorylation site ...
Leukaemia Section t(9;22)(q34;q11) in ANLL Atlas of Genetics and Cytogenetics
... The crucial event lies on der(22), id est 5' BCR/3' ABL hybrid gene is pathogenic, while ABL/BCR may or may not be expressed; Breakpoint in ABL is variable over a region of 200 kb, often between the two alternative exons 1b and 1a, sometimes 5' of 1b, or 3' of 1a, but always 5' of exon 2; Breakpoint ...
... The crucial event lies on der(22), id est 5' BCR/3' ABL hybrid gene is pathogenic, while ABL/BCR may or may not be expressed; Breakpoint in ABL is variable over a region of 200 kb, often between the two alternative exons 1b and 1a, sometimes 5' of 1b, or 3' of 1a, but always 5' of exon 2; Breakpoint ...
Section 3A Analysis on a Western Blot
... complex mixtures such as cell or membrane extracts (for instance, Canfield and Levenson, 1993; Duden et al., 1991). When combined with immunoprecipitation (as described in Section 4.D of this manual), it can reveal information about the interaction of the tagged protein with other cell components (f ...
... complex mixtures such as cell or membrane extracts (for instance, Canfield and Levenson, 1993; Duden et al., 1991). When combined with immunoprecipitation (as described in Section 4.D of this manual), it can reveal information about the interaction of the tagged protein with other cell components (f ...
Lecture 17 Expanded Genetic Code
... identity element in every tRNA except for proline in E. coli ...
... identity element in every tRNA except for proline in E. coli ...
Docking Studies in Target Proteins Involved in Antibacterial Action
... taking into account that ILA, the co-crystallyzed ligand inhibitor, presents an experimental Ki value of 0.006 µM. Otherwise, other mechanism of protein synthesis inhibition cannot be excluded. The protein targets involved in nucleic acid synthesis (DNA gyrase and TopoIV) have two active sites. Here ...
... taking into account that ILA, the co-crystallyzed ligand inhibitor, presents an experimental Ki value of 0.006 µM. Otherwise, other mechanism of protein synthesis inhibition cannot be excluded. The protein targets involved in nucleic acid synthesis (DNA gyrase and TopoIV) have two active sites. Here ...
Support Vector Machine-based classification of protein folds using
... frequencies of amino acids gave an overall accuracy of 65.2% for fold discrimination, which is better than the accuracy by any method reported so far in the literature. Combination of secondary structural state frequencies with solvent accessibility state frequencies of amino acids and amino acid pa ...
... frequencies of amino acids gave an overall accuracy of 65.2% for fold discrimination, which is better than the accuracy by any method reported so far in the literature. Combination of secondary structural state frequencies with solvent accessibility state frequencies of amino acids and amino acid pa ...
Process Biochemistry
... acid or alkaline pH (A1 and B1) and were recovered in the protein isolate (A3 and B3). In the water at the end of the process (A4 and B4), MHC and the other myofibril proteins are not present, having been effectively and efficiently precipitated and collected after the second centrifugation. The solub ...
... acid or alkaline pH (A1 and B1) and were recovered in the protein isolate (A3 and B3). In the water at the end of the process (A4 and B4), MHC and the other myofibril proteins are not present, having been effectively and efficiently precipitated and collected after the second centrifugation. The solub ...
Review Article Protein aggregation and degradation mechanisms in
... to different intracellular compartments. After misfolding, most proteins are recognized and ubiquitinated, which directs them to the JUNQ, a region that contains chaperones and 26S proteasomes. JUNQ concentrates soluble misfolded proteins, which may be proteasomally degraded or refolded by the chape ...
... to different intracellular compartments. After misfolding, most proteins are recognized and ubiquitinated, which directs them to the JUNQ, a region that contains chaperones and 26S proteasomes. JUNQ concentrates soluble misfolded proteins, which may be proteasomally degraded or refolded by the chape ...
Generation of polyclonal antiserum for the detection
... peptide) containing TFA/H2O/TIPS in ratios of 95/2.5/ 2.5 were prepared immediately prior to use. The peptide resins were swollen in DCM, filtered and cleavage cocktail was added and capped under N2. The time for cleavage/deprotection (1 to 5 h) was established according to real time RP HPLC separat ...
... peptide) containing TFA/H2O/TIPS in ratios of 95/2.5/ 2.5 were prepared immediately prior to use. The peptide resins were swollen in DCM, filtered and cleavage cocktail was added and capped under N2. The time for cleavage/deprotection (1 to 5 h) was established according to real time RP HPLC separat ...
Modern applications of amino acids and dipeptides
... have also been used as soluble equivalents in parenteral nutrition, and both the glycine and alanine dipeptides have been shown to be readily hydrolysed in vivo (21). l-Alanyl-l-tyrosine (18a) and l-alanyl-l-cystine (19) have been tested in CHO cells, and shown to give improved cell viability and ce ...
... have also been used as soluble equivalents in parenteral nutrition, and both the glycine and alanine dipeptides have been shown to be readily hydrolysed in vivo (21). l-Alanyl-l-tyrosine (18a) and l-alanyl-l-cystine (19) have been tested in CHO cells, and shown to give improved cell viability and ce ...
Biological monomers and polymers (1)
... That is why all starches tend close-up to look alike (carrot or baobab), while proteins look startlingly different. Elements such as C, H, O, N, P and S (also called macro elements) make up biomolecules and are therefore the largest dry weight of all living organisms. Other elements are present in s ...
... That is why all starches tend close-up to look alike (carrot or baobab), while proteins look startlingly different. Elements such as C, H, O, N, P and S (also called macro elements) make up biomolecules and are therefore the largest dry weight of all living organisms. Other elements are present in s ...
PDF (SLMChapter1)
... using the transfection reagent Effectene (Qiagen) [47]. They observed suppression of chloramphenicol acetyl transferase, mutated to contain the corresponding stop codon within the coding region. Lastly, Vogel and coworkers demonstrated nonsense suppression of EGFP with aminoacyl-tRNA [48]. They micr ...
... using the transfection reagent Effectene (Qiagen) [47]. They observed suppression of chloramphenicol acetyl transferase, mutated to contain the corresponding stop codon within the coding region. Lastly, Vogel and coworkers demonstrated nonsense suppression of EGFP with aminoacyl-tRNA [48]. They micr ...
Summary-1
... Significant differences in the SMOA(Helix) and PHBH(Sheet) secondary structure. Also steric problem with SMOA loop piercing through adenosine ring. Suggests an alternate FAD-binding mode in SMOA. This may contibute to the weak binding of Oxidized FAD to SMOA. ...
... Significant differences in the SMOA(Helix) and PHBH(Sheet) secondary structure. Also steric problem with SMOA loop piercing through adenosine ring. Suggests an alternate FAD-binding mode in SMOA. This may contibute to the weak binding of Oxidized FAD to SMOA. ...
Statistical analysis of DNA microarray data
... glycylation, covalent linkage of one to more than 40 glycine residues to the tubulin Cterminal tail glycosylation, the addition of a glycosyl group to either asparagine, hydroxylysine, serine, or threonine, resulting in a glycoprotein isoprenylation, the addition of an isoprenoid group (e.g. farneso ...
... glycylation, covalent linkage of one to more than 40 glycine residues to the tubulin Cterminal tail glycosylation, the addition of a glycosyl group to either asparagine, hydroxylysine, serine, or threonine, resulting in a glycoprotein isoprenylation, the addition of an isoprenoid group (e.g. farneso ...
Application 1
... nanoparticles can serve as useful detection and targeting agents. These AuNPs when encapsulated with carbohydrate ligands can serve as a useful affinity probe for rapid, efficient separation of target proteins followed by on-probe analysis using mass spectroscopy. This technique of protein targeting ...
... nanoparticles can serve as useful detection and targeting agents. These AuNPs when encapsulated with carbohydrate ligands can serve as a useful affinity probe for rapid, efficient separation of target proteins followed by on-probe analysis using mass spectroscopy. This technique of protein targeting ...
Polar location and functional domains of the Agrobacterium
... to the cell poles. Quantitative analysis indicated that about 95% of the foci localized to the cell poles (Table 3). About 50% of the cells exhibited multiple foci of fluorescence. In these bacteria, the protein localized to other areas of the membranes including the poles. Strains with mutations in ...
... to the cell poles. Quantitative analysis indicated that about 95% of the foci localized to the cell poles (Table 3). About 50% of the cells exhibited multiple foci of fluorescence. In these bacteria, the protein localized to other areas of the membranes including the poles. Strains with mutations in ...
Biochemistry
... (4) Physicochemical properties of amino acids: isoelectric point, amino acid may have different charge, ultraviolet absorption, reaction with ninhydrin (5) The α-group determin the properties of individual amino acids 2. Peptides (1) L-amino acids linked by peptide bonds form peptides : peptide, oli ...
... (4) Physicochemical properties of amino acids: isoelectric point, amino acid may have different charge, ultraviolet absorption, reaction with ninhydrin (5) The α-group determin the properties of individual amino acids 2. Peptides (1) L-amino acids linked by peptide bonds form peptides : peptide, oli ...
The Dock and Lock Method: A Novel
... human carcinoembryonic antigen (CEACAM5). The first A, C-DDD1-Fab-hMN-14, was generated by linking the DDD1 peptide sequence, which is composed of amino acids 1 to 44 of human RIIa, to the COOH-terminal end of the Fd chain via a 14-residue flexible peptide linker (Fig. 2B). This construct was modifi ...
... human carcinoembryonic antigen (CEACAM5). The first A, C-DDD1-Fab-hMN-14, was generated by linking the DDD1 peptide sequence, which is composed of amino acids 1 to 44 of human RIIa, to the COOH-terminal end of the Fd chain via a 14-residue flexible peptide linker (Fig. 2B). This construct was modifi ...
Protein diffusion in plant cell plasma membranes
... Interestingly, the fluorescence recovery curve of PM proteins describes the sum of at least two additive mechanisms: the lateral mobility of the protein within the PM, and the exchange of proteins between cytoplasmic vesicles and the PM by endocytosis and exocytosis. It is possible to distinguish be ...
... Interestingly, the fluorescence recovery curve of PM proteins describes the sum of at least two additive mechanisms: the lateral mobility of the protein within the PM, and the exchange of proteins between cytoplasmic vesicles and the PM by endocytosis and exocytosis. It is possible to distinguish be ...
Flower`n`Fruit
... Methionine: This is an ethylene precursor, which increases the quality and quantity of production. Proline: Its main function is to maintain the plant’s hydrous balance in the cell walls, resisting adverse conditions (drought, salinity, etc.). It increases the percentage of pollen grain germination, ...
... Methionine: This is an ethylene precursor, which increases the quality and quantity of production. Proline: Its main function is to maintain the plant’s hydrous balance in the cell walls, resisting adverse conditions (drought, salinity, etc.). It increases the percentage of pollen grain germination, ...
Targeted Proteomic Study of the Cyclin
... (Cdc2) functions with one of two G1 cyclins (Cig1 and 2) and one B type cyclin (Cdc13). In vertebrates (including humans), at least eight Cdks function with at least nine cyclins where only some cyclin-Cdk combinations are functional and where tissue specificity adds another level of complexity (rev ...
... (Cdc2) functions with one of two G1 cyclins (Cig1 and 2) and one B type cyclin (Cdc13). In vertebrates (including humans), at least eight Cdks function with at least nine cyclins where only some cyclin-Cdk combinations are functional and where tissue specificity adds another level of complexity (rev ...
Full Text PDF - International Journal of Computational Bioinformatics
... Result of present investigation indicates that G8 protein of Homo sapiens and the likely protein present in other organisms are non-cytoplasmic (Figure 3a and 3b) and contain a transmembrane region to be characterized as a half transporter. Out of five proteins two can be categorized as ABC transpor ...
... Result of present investigation indicates that G8 protein of Homo sapiens and the likely protein present in other organisms are non-cytoplasmic (Figure 3a and 3b) and contain a transmembrane region to be characterized as a half transporter. Out of five proteins two can be categorized as ABC transpor ...
Protein
Proteins (/ˈproʊˌtiːnz/ or /ˈproʊti.ɨnz/) are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues. Proteins perform a vast array of functions within living organisms, including catalyzing metabolic reactions, DNA replication, responding to stimuli, and transporting molecules from one location to another. Proteins differ from one another primarily in their sequence of amino acids, which is dictated by the nucleotide sequence of their genes, and which usually results in protein folding into a specific three-dimensional structure that determines its activity.A linear chain of amino acid residues is called a polypeptide. A protein contains at least one long polypeptide. Short polypeptides, containing less than about 20-30 residues, are rarely considered to be proteins and are commonly called peptides, or sometimes oligopeptides. The individual amino acid residues are bonded together by peptide bonds and adjacent amino acid residues. The sequence of amino acid residues in a protein is defined by the sequence of a gene, which is encoded in the genetic code. In general, the genetic code specifies 20 standard amino acids; however, in certain organisms the genetic code can include selenocysteine and—in certain archaea—pyrrolysine. Shortly after or even during synthesis, the residues in a protein are often chemically modified by posttranslational modification, which alters the physical and chemical properties, folding, stability, activity, and ultimately, the function of the proteins. Sometimes proteins have non-peptide groups attached, which can be called prosthetic groups or cofactors. Proteins can also work together to achieve a particular function, and they often associate to form stable protein complexes.Once formed, proteins only exist for a certain period of time and are then degraded and recycled by the cell's machinery through the process of protein turnover. A protein's lifespan is measured in terms of its half-life and covers a wide range. They can exist for minutes or years with an average lifespan of 1–2 days in mammalian cells. Abnormal and or misfolded proteins are degraded more rapidly either due to being targeted for destruction or due to being unstable.Like other biological macromolecules such as polysaccharides and nucleic acids, proteins are essential parts of organisms and participate in virtually every process within cells. Many proteins are enzymes that catalyze biochemical reactions and are vital to metabolism. Proteins also have structural or mechanical functions, such as actin and myosin in muscle and the proteins in the cytoskeleton, which form a system of scaffolding that maintains cell shape. Other proteins are important in cell signaling, immune responses, cell adhesion, and the cell cycle. Proteins are also necessary in animals' diets, since animals cannot synthesize all the amino acids they need and must obtain essential amino acids from food. Through the process of digestion, animals break down ingested protein into free amino acids that are then used in metabolism.Proteins may be purified from other cellular components using a variety of techniques such as ultracentrifugation, precipitation, electrophoresis, and chromatography; the advent of genetic engineering has made possible a number of methods to facilitate purification. Methods commonly used to study protein structure and function include immunohistochemistry, site-directed mutagenesis, X-ray crystallography, nuclear magnetic resonance and mass spectrometry.