Cell Membranes In Red Blood Cells

The citric acid cycle, also called the Krebs cycle or the tricarboxylic acid, TCA, cycle, a series of chemical reactions that generates energy from the oxidation of acetate into chemical energy and carbon dioxide in the form of ATP. It also provides NADH, which is a reducing agent that is very common in biochemical reactions. This cycle is constantly supplied with new carbon. This comes in from acetyl-CoA, which starts the entire process of the citric acid cycle. The first step of the citric acid cycle is the aldol condensation of oxaloacetate and acetyl-CoA and water with the enzyme citrate synthase in order to form citrate and CoA-SH. The next step is the dehydration of citrate with the enzyme aconitase in order to form cis-aconitate and water. Then comes the hydration of cis-Aconitate and water with the enzyme aconitase in order to form isocitrate. The next is the oxidation of isocitrate and NAD+ with the enzyme isocitrate dehydrogenase in order to form oxalosuccinate and NADH and H+. Then, there is the decarboxylation of oxalosuccinate with the enzyme isocitrate dehydrogenase in order to form alpha-ketoglutarate and carbon dioxide. Next, there is the oxidative decarboxylation of alpha-ketoglutarate and NAD+ and CoA-SH with the enzyme alpha-ketoglutarate dehydrogenase in order to form succinyl-CoA and NADH and H+ and carbon dioxide. The next step is the substrate-level phosphorylation of succinyl-CoA and GDP and Pi with the enzyme succinyl-CoA synthetase in order to form succinate and CoA-SH and GTP. Then, there is the oxidation of succinate and ubiquinone with the enzyme succinate dehydrogenase in order to form fumarate and ubiquinol. Next, is the hydration of fumarate and water with the enzyme fumarase in order to form L-malate. The final step is the oxidation of L-malate and NAD+ with the enzyme malate dehydrogenase in order to form oxaloacetate and NADH and H+. Two cycles are required for every single glucose molecule because two acetyl Co-A molecules

Aerobic respiration happens only when oxygen is presented in the cell. Aerobic respiration starts with pyruvate crossing into the mitochondria. When it passes through, a Coenzyme A will attach to it producing Acetyl CoA, CO2, and NADH. Acetyl CoA will enter into the Krebs cycle. In the Krebs cycle Acetyl CoA will bound with Oxaloacetic Acid (OAA), a four carbon molecule, producing the six carbon molecule, Citric Acid. Citric Acid will reorganize into Isocitrate. This will lose a CO2 and make a NADH turning itself into alpha ketoglutarate, a five carbon molecule. Alpha ketoglutarate will turn into an unstable four carbon molecule, which attaches to CoA making succinyl CoA. During that process a CO2 and NADH is made. An ATP is made when CoA leaves and creates Succinate. This molecule is turned into Fumarate, creating two FADH2 in the process. Then Fumarate is turned into Malate then into OAA making two NADH. Only two ATP is produced in Krebs cycle but the resulting NADHs and FADH2s are passed through an electron transport chain and ATP synthase. When the molecules passes through that cycle a total of 28 ATP molecules are produced. In all aerobic respiration produces 32 ATP and waste products of H2O and

The body has two faces, the cis face which fuses with incoming transport vesicles, and the trans face which excretes the secretory vesicles. The cis face fuses with vesicles coming from the ER effectively from many directions due to its convex shape, whereas the concave trans face can direct the secretory vesicles to their destination. When fusing with the cis face, the transport vesicles release their proteins to be absorbed for modification. Each cisternal layer of the Golgi body holds different enzymes which each modify the passing proteins in separate ways. Between the layers the proteins are moved through the gaps by small vesicles. When a protein has been modified correctly, it leaves the Golgi body via secretory vesicles which then carry the modified proteins to the cell membrane or another organelle. The proteins that are transported to the cell membrane are either excreted from the cell, or absorbed into the membrane to aid with its function. Some of the secretory vesicles which hold hydrolytic enzymes stay within the cytoplasm and function as lysosomes.

In contrast, there are four metabolic stages happened in cellular respiration, which are the glycolysis, the citric acid cycle, and the oxidative phosphorylation. Glycolysis occurs in the cytoplasm, in which catabolism is begun by breaking down glucose into two molecules of pyruvate. Two molecules of ATP are produced too. Some of they either enter the citric acid cycle (Krebs cycle) or the electron transport chain, or go into lactic acid cycle if there is not enough oxygen, which produces lactic acid. The citric acid cycle occurs in the mitochondrial matrix, which completes the breakdown of glucose by oxidizing a derivative of pyruvate into carbon dioxide. The citric acid cycle produced some more ATPs and other molecules called NADPH and FADPH. After this, electrons are passed to the electron transport chain through

It moves through the cell membrane to a set location. It marks proteins with a signal

In this lab experiment, half our group observed and measured osmosis using dialysis tubes that were represented as the semipermeable membrane. It is permeable to water and other small molecules but is impermeable to larger molecules such as the sucrose solution used in each of the four beakers and tubing. The other half of our group observed the tonicity of sheep blood to determine whether the blood was isotonic, hypotonic, or hypertonic. The 85 g/dL of NaCl solution was the ideal isotonic number in relation to the sheep blood cells as well as a reference to the other observations of the solutions.

Second, in order to further confirm the information about characteristics and function of the targeting protein that we have

However this is not as simple as it looks and the whole thing is actually a five step process. Step 1: Pyruvate is decarboxylated by pyruvate dehydrogenase with help from TPP. Step 2: The reactive carbon of the TPP is oxidized and transferred as the acetyl group to lipoamide. This forms hydroxyethyl-TPP. An H+ ion is required for the intermediate to give off CO2.

The Golgi packages proteins inside membrane-bound vesicles before sending them to their destination, whether it is outside the cell or somewhere else inside the cell.

Eukaryotic organisims have an advanced system of intracellular organelles. Each organelle membrane has a specific arrangement of proteins and lipids. Inside cell, an acurate and highly co-ordinated vesicular trafficking pathways operate for establishment and maintenance of compartmentalization. This intracellular compartments creates specialized environments for various chemical reactions, important for cellular function (Warren and Mellman 2006). The trafficking process begins with the budding of transport vesicles from donor membranes and ends with their fusion to target organelles. A single round in the transport process (vesicle budding to its fusion) involves two classes of RAS-like, small GTPase family proteins (serve as switch

Proteins serve a myriad of functions whether within or outside of the cells. These functions include structural roles (cytoskeleton), transport of

The Krebs cycle is a series of reactions which occur in the mitochondria and results in the formation of ATP and other molecules which undergo farther reactions to form more ATP. Cellular respiration can be divided into four sequences. The first sequence is glycolysis, its breaks down one molecule glucose into two molecules pyruyate. Transition takes place in the matrix of the mitochondria and it’s referred to the beginning of aerobic respiration. The process takes place if there is enough amounts of oxygen in the mitochondria. However if there is insufficient oxygen in the mitochondria it could result into fermentation. Transition Reactions take place in the pyruvate molecule. In transition reactions two hydrogen electrons and one carbon

Glycolysis is followed by the Krebs cycle, however, this stage does require oxygen and takes place in the mitochondria. During the Krebs cycle, pyuvic acid is broken down into carbon dioxide in a series of energy-extracting reactions. This begins when pyruvic acid produced by glycolysis enters the mitochondria. As the cycle continues, citric acid is broken down into a 4-carbon molecule and more carbon dioxide is released. Then, high-energy electrons are passed to electron carriers and taken to the electron transport chain. All this produces 2 ATP, 6 NADH, 2 FADH, and 4 CO2 molecules.

The membrane of the red blood cell plays many roles that aid in regulating their surface deformability, flexibility, adhesion to other cells and immune recognition. These functions are highly dependent on its composition, which defines its properties. The red blood cell membrane is composed of 3 layers: the glycocalyx on the exterior, which is rich in carbohydrates; the lipid bilayer which contains many transmembrane proteins, besides its lipidic main constituents; and the membrane skeleton, a structural network of proteins located on the inner surface of the lipid bilayer. In human erythrocytes, like in most mammal erythrocytes, half of the membrane mass is represented by proteins and the other half are lipids, namely phospholipids and cholesterol.[29]

Overexpression of the HEPN domain in HeLa cells following three hours of starvation indicates that sacsin plays a key role in lysosomal transport due to the reduced efficiency of perinuclear lysosomal clustering. HEPN’s property of dimerizing may be disrupting the function of with full-length sacsin by preventing endogenous sacsin from dimerizing within the cell. Thus, dimerization may be essential to sacsin’s function, particularly for binding JIP3, which is necessary for lysosomal transport7. HATPase 3 overexpression may be occupying JIP3 binding, but was not found to disrupt lysosomal localization following starvation, perhaps due to the truncated size of this deletion construct.