
The enemy within: ricin and plant cells
... masquerade as a misfolded protein, perhaps after reduction of the interchain disulphide bond which would expose a hydrophobic patch at the C-terminus of RTA that is normally shielded by RTB. This, however, remains to be experimentally established. Whatever the events, the fact that export of protein ...
... masquerade as a misfolded protein, perhaps after reduction of the interchain disulphide bond which would expose a hydrophobic patch at the C-terminus of RTA that is normally shielded by RTB. This, however, remains to be experimentally established. Whatever the events, the fact that export of protein ...
Changes in Typical Organelles in Developing Cotyledons of Soybean
... were also recognized (Figs. 3C, 30) . These organelles were distinctly stained by PAS, CBB and osmium and could also be distinguished from other structures by their spherical shape . Their number and size increased around 30 OAF. Until they are better understood, we are calling these organelles prot ...
... were also recognized (Figs. 3C, 30) . These organelles were distinctly stained by PAS, CBB and osmium and could also be distinguished from other structures by their spherical shape . Their number and size increased around 30 OAF. Until they are better understood, we are calling these organelles prot ...
HIS-Select Nickel Affinity Gel (P6611) - Technical - Sigma
... 6. Wash the affinity gel two times with at least 500 µl of Wash Buffer without imidazole. Gently mix the affinity gel for 10 seconds, then centrifuge for 30 seconds at 5,000 × g. Save the Wash Buffer solutions for analysis either as a single pool or three fractions. 7. Elute the target protein with ...
... 6. Wash the affinity gel two times with at least 500 µl of Wash Buffer without imidazole. Gently mix the affinity gel for 10 seconds, then centrifuge for 30 seconds at 5,000 × g. Save the Wash Buffer solutions for analysis either as a single pool or three fractions. 7. Elute the target protein with ...
From Amino Acid to Glucosinolate Biosynthesis: Protein Sequence
... up to six methylene groups and thus is an important determinant of glucosinolate variability in this plant. The committed step in Met side chain elongation is catalyzed by methylthioalkylmalate synthase (MAM) (Kroymann et al., 2001; Textor et al., 2004, 2007; Benderoth et al., 2006), and this enzyme ...
... up to six methylene groups and thus is an important determinant of glucosinolate variability in this plant. The committed step in Met side chain elongation is catalyzed by methylthioalkylmalate synthase (MAM) (Kroymann et al., 2001; Textor et al., 2004, 2007; Benderoth et al., 2006), and this enzyme ...
The Effect of Chemical Treatments of Albumin and Orosomucoid on
... albumin was subjected increase to varying degrees the affinity of the albumin molecule for binding sites on that region of the plasma membrane from which pinocytic vesicles are formed. Some comparable experiments with native and desialylated human orosomucoid indicate that the rat yolk-sac epithelia ...
... albumin was subjected increase to varying degrees the affinity of the albumin molecule for binding sites on that region of the plasma membrane from which pinocytic vesicles are formed. Some comparable experiments with native and desialylated human orosomucoid indicate that the rat yolk-sac epithelia ...
Predicting DNA-binding sites of proteins from amino acid sequence
... Background: Understanding the molecular details of protein-DNA interactions is critical for deciphering the mechanisms of gene regulation. We present a machine learning approach for the identification of amino acid residues involved in protein-DNA interactions. Results: We start with a Naïve Bayes c ...
... Background: Understanding the molecular details of protein-DNA interactions is critical for deciphering the mechanisms of gene regulation. We present a machine learning approach for the identification of amino acid residues involved in protein-DNA interactions. Results: We start with a Naïve Bayes c ...
Molecular design of the photosystem II light
... energy dissipation would result. Indeed, it has been recognized that the maximum fluorescence lifetime of chlorophyll in vivo is always less than free chlorophyll or chlorophyll in unaggregated LHCII (Horton and Ruban, 1994). Perhaps the advantages of oligomeric organization outweigh the disadvantag ...
... energy dissipation would result. Indeed, it has been recognized that the maximum fluorescence lifetime of chlorophyll in vivo is always less than free chlorophyll or chlorophyll in unaggregated LHCII (Horton and Ruban, 1994). Perhaps the advantages of oligomeric organization outweigh the disadvantag ...
Translation - e
... 1. It has to translate code written with an alphabet of 4 bases in a second written by 20 amino acids! 2. It has to synthesize protein (peptidyl transferase reaction)! 3. It has to guarantee the moving on the mRNA and tRNA molecules exchange! ...
... 1. It has to translate code written with an alphabet of 4 bases in a second written by 20 amino acids! 2. It has to synthesize protein (peptidyl transferase reaction)! 3. It has to guarantee the moving on the mRNA and tRNA molecules exchange! ...
DNA Specificity of the Bicoid Activator Protein Is Determined by
... proteins distinguish between these sites using residues in the recognition helix which differ, and are in positions corresponding to those important for repressor-DNA recognition. In this study, we employed fusion proteins that contain the DNA binding domains of the bacterial LexA repressor or the y ...
... proteins distinguish between these sites using residues in the recognition helix which differ, and are in positions corresponding to those important for repressor-DNA recognition. In this study, we employed fusion proteins that contain the DNA binding domains of the bacterial LexA repressor or the y ...
PDF - University of California, San Francisco
... We present and evaluate a model for the secondary structure and membrane orientation of 3-hydroxy-3methylglutaryl coenzyme A reductase, the glycoprotein of the endoplasmic reticulum that controls the rate of cholesterol biosynthesis. This model is derived from proteolysis experiments that separate t ...
... We present and evaluate a model for the secondary structure and membrane orientation of 3-hydroxy-3methylglutaryl coenzyme A reductase, the glycoprotein of the endoplasmic reticulum that controls the rate of cholesterol biosynthesis. This model is derived from proteolysis experiments that separate t ...
Document
... A. Two pathways: Biosynthetic secretory and endocytic, Fig. 13-1 B. The process of transport between all parts of the pathway is identical, vesicular transport, Fig. 13-2. C. Experimental Methods for studying vesicular transport 1. Cell free systems 2. Genetic 3. GFP fusion proteins D Specificity of ...
... A. Two pathways: Biosynthetic secretory and endocytic, Fig. 13-1 B. The process of transport between all parts of the pathway is identical, vesicular transport, Fig. 13-2. C. Experimental Methods for studying vesicular transport 1. Cell free systems 2. Genetic 3. GFP fusion proteins D Specificity of ...
Isolation of a Strong Suppressor of Nonsense Mutations in Bacillus
... The above results strongly suggest that the B. suhtilis strain S U + ~contains an ochre suppressor and B. subtilis su+44 an amber suppressor. Mutant susB47 would contain an ochre mutation being suppressed by S U + ~but not by S U + ~ ~In. the case of revertant susB610, an A to G transition in the th ...
... The above results strongly suggest that the B. suhtilis strain S U + ~contains an ochre suppressor and B. subtilis su+44 an amber suppressor. Mutant susB47 would contain an ochre mutation being suppressed by S U + ~but not by S U + ~ ~In. the case of revertant susB610, an A to G transition in the th ...
2.3 Carbon-Based Molecules
... things • What are bigger molecules called? What are the smaller molecules that join together to make big molecules called? • What atoms must be removed from monomers to make polymers? What is this process called? ...
... things • What are bigger molecules called? What are the smaller molecules that join together to make big molecules called? • What atoms must be removed from monomers to make polymers? What is this process called? ...
De Novo Pyrimidine Nucleotide Synthesis Mainly
... INTRODUCTION Nucleotides are building blocks of RNA. Both nucleotides and RNA are among the first biomolecules to arise in the evolution of life long before DNA and proteins came into play (Joyce, 2002). Since that time, nucleotide and nucleic acid metabolism have constituted a central part of the m ...
... INTRODUCTION Nucleotides are building blocks of RNA. Both nucleotides and RNA are among the first biomolecules to arise in the evolution of life long before DNA and proteins came into play (Joyce, 2002). Since that time, nucleotide and nucleic acid metabolism have constituted a central part of the m ...
Two-step and one-step secretion mechanisms in Gram
... machineries for transport of substrates across their cell membrane in response to various environmental cues. These machineries, known as secretion systems, are essential for bacterial virulence and are used by bacteria to acquire nutrients, transport various proteins, nucleic acids or toxins or ass ...
... machineries for transport of substrates across their cell membrane in response to various environmental cues. These machineries, known as secretion systems, are essential for bacterial virulence and are used by bacteria to acquire nutrients, transport various proteins, nucleic acids or toxins or ass ...
Supplementary Figures 1 - 5, Methods
... The expression of Globo-H on (A) MCF-7 cells and (B) MDA-MB-157 cells was determined by flow cytometry with mAbVK9. (C) Microvesicles (MVs, 50g) harvested from the supernatants of MDA-MB-157 cells (MB-MVs) were incubated with HUVECs for 4h and examined for surface Globo-H. (D) Serial dilutions of M ...
... The expression of Globo-H on (A) MCF-7 cells and (B) MDA-MB-157 cells was determined by flow cytometry with mAbVK9. (C) Microvesicles (MVs, 50g) harvested from the supernatants of MDA-MB-157 cells (MB-MVs) were incubated with HUVECs for 4h and examined for surface Globo-H. (D) Serial dilutions of M ...
Activity 3
... optical density measurements between tubes 1 and 2. The boiling of the solution in test tube 1 caused the denaturing of pepsin, rendering this inactive and unable to digest BAPNA. ...
... optical density measurements between tubes 1 and 2. The boiling of the solution in test tube 1 caused the denaturing of pepsin, rendering this inactive and unable to digest BAPNA. ...
2.2.56. amino acid analysis
... and cysteine is typically recovered as cystine (but cystine recovery is usually poor because of partial destruction or reduction to cysteine). Application of adequate vacuum (less than 200 µm of mercury or 26.7 Pa) or introduction of an inert gas (argon) in the headspace of the reaction vessel can r ...
... and cysteine is typically recovered as cystine (but cystine recovery is usually poor because of partial destruction or reduction to cysteine). Application of adequate vacuum (less than 200 µm of mercury or 26.7 Pa) or introduction of an inert gas (argon) in the headspace of the reaction vessel can r ...
De Novo Pyrimidine Nucleotide Synthesis Mainly
... INTRODUCTION Nucleotides are building blocks of RNA. Both nucleotides and RNA are among the first biomolecules to arise in the evolution of life long before DNA and proteins came into play (Joyce, 2002). Since that time, nucleotide and nucleic acid metabolism have constituted a central part of the m ...
... INTRODUCTION Nucleotides are building blocks of RNA. Both nucleotides and RNA are among the first biomolecules to arise in the evolution of life long before DNA and proteins came into play (Joyce, 2002). Since that time, nucleotide and nucleic acid metabolism have constituted a central part of the m ...
The Emerging Role of Branched-Chain Amino Acids in Insulin
... risk [23]. The association between BCAA signature and IR was supported by Fiehn’s study which showed that leucine and valine among >350 metabolites were increased in African-American T2DM women subjects [24]. It was further confirmed in a cross-sectional study of 73 overweight/obese individuals with ...
... risk [23]. The association between BCAA signature and IR was supported by Fiehn’s study which showed that leucine and valine among >350 metabolites were increased in African-American T2DM women subjects [24]. It was further confirmed in a cross-sectional study of 73 overweight/obese individuals with ...
UvA-DARE (Digital Academic Repository) Mitochondria in neutrophil
... XIAP is a closely related protein. Most of the non-apoptotic caspases play a role in processing regulatory cytokines of the immune system or are involved in immune signaling 16. It is, therefore, not surprising that immune signaling and apoptosis are such closely related processes. The TNF-α recepto ...
... XIAP is a closely related protein. Most of the non-apoptotic caspases play a role in processing regulatory cytokines of the immune system or are involved in immune signaling 16. It is, therefore, not surprising that immune signaling and apoptosis are such closely related processes. The TNF-α recepto ...
Integrating the universal metabolism into a phylogenetic analysis
... depending on the amino acid (oxoglutarate, succinyl-CoA, oxaloacetate, or acetyl-CoA). The Krebs cycle is divided into two parts, designated using the two main points of entrance: KC1 from oxaloacetate to oxoglutarate and KC2 from oxoglutarate to oxaloacetate. The urea cycle is not delineated in ref ...
... depending on the amino acid (oxoglutarate, succinyl-CoA, oxaloacetate, or acetyl-CoA). The Krebs cycle is divided into two parts, designated using the two main points of entrance: KC1 from oxaloacetate to oxoglutarate and KC2 from oxoglutarate to oxaloacetate. The urea cycle is not delineated in ref ...
Characterization of the binding properties of the Avian Coronavirus
... Protein biochemistry ................................................................................. 47 ...
... Protein biochemistry ................................................................................. 47 ...
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.