Sandbox Reserved 470

This Sandbox is Reserved from 13/03/2012, through 01/06/2012 for use in the course "Proteins and Molecular Mechanisms" taught by Robert B. Rose at the North Carolina State University, Raleigh, NC USA. This reservation includes Sandbox Reserved 451 through Sandbox Reserved 500.

To get started: Click the edit this page tab at the top. Save the page after each step, then edit it again. Click the 3D button (when editing, above the wikitext box) to insert Jmol. show the Scene authoring tools, create a molecular scene, and save it. Copy the green link into the page. Add a description of your scene. Use the buttons above the wikitext box for bold, italics, links, headlines, etc. More help: Help:Editing For more help, look at this link: https://www.proteopedia.org/wiki/index.php/Help:Getting_Started_in_Proteopedia Introduction Glyceraldehyde-3-phosphate Dehydrogenase spinqualitylabelsall models Glyceraldehyde-3-phosphate Dehydrogenase Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D (abbreviated as GAPDH or the less common G3PDH) (EC 1.2.1.12) ~37kDa is a well-known enzyme which catalyzes the sixth step of glycolysis, a reversible cytosolic process in eukaryotes which involves the breakdown of glucose for energy and carbon molecules. Along with its role in glycolysis and gluconeogenesis, recent research has determined that GAPDH is actually a multifunctional protein, as it has numerous defined, non-metabolic functions involved in multiple subcellular processes including transcription activation, ER to Golgi transportation, transcriptional control of histone gene expression, nuclear membrane fusion, neuronal initiation of apoptosis, microtubule bundling, phosphotransferase activity, prostate cancer progression, recognizing fraudulently incorporated nucleotides in DNA, and maintaining telomere structures. Research also shows that it possibly has a direct involvement in cellular phenotype of human neurodegenerative disorders, especially those characterized by expansion of CAG repeats. Structure GAPDH has two domains, a GAPDH-like, C-terminal domain, and an NAD Binding Domain. The NAD (Nucleotide) Binding Domain is an Alpha Beta 3-Layer(α-β-α) Sandwich, including amino acids 1-138 and 301-340 on chains O and Q . Its CATH reports a Rossmann fold and a classification as an oxidoreductase. The GAPDH-like, C-terminal domain (Catalytic domain) is an Alpha Beta 2-Layer(α-β) Sandwich, including amino acids 139 - 300 on chains O and Q . Its CATH reports a holo-D-Glyceraldehyde-3-Phosphate Dehydrogenase, (domain 2) and a classification as an oxidoreductase (aldehyde(D)-NAD(A)). Importance Role in Glycolysis: The Steps: In two coupled steps, GAPDH catalyzes the conversion of glyceraldyhyde-3-phosphate at carbon 1 to 1,3-bisphosphoglycerate (1,3-BPG). The Reactions: The reaction involving the GAPDH enzyme combines phosphorylation with oxidation in an overall endergonic reaction. (ΔG°'=+6.3 kJ/mol (+1.5 kcal/mol)) First, the oxidation of glyceraldyhyde-3-phosphate to D-glycerate 1,3-bisphosphate takes place, in which an aldehyde is converted to carboxylic acid ((ΔG°'=-50 kJ/mol (-12 kcal/mol))and NAD+ (Nicotinamide adenine dinucleotide), an important co-factor and ligand found bound to the active site of GAPDH, is simultaneously reduced endergonically to NADH. This oxidation reaction is required for the initiation of the second reaction because it is highly exergonic and thus drives the endergonic second reaction ((ΔG°'=+50 kJ/mol (+12 kcal/mol)). In the second reaction a molecule of inorganic phosphate is transferred to a GAP intermediate to form a product with a high potential to transfer phosphates, 1,3-bisphosphoglycerate. The Mechanism: The mechanism of GAPDH is mainly dependent the thiol functional group on a cysteine residue, of the 3-phosphoglycerate amino acid biosynthetic family, which lies within the active site. This important thiol group acts as a nucleophile, attacking the carbon on the aldehyde functional group of the substrate, glyceraldehyde 3-phosphate, after it binds to GAPDH. The creation of a thiohemiacetal intermediate occurs from this oxidative reaction, which then loses a hydride to NAD+, which is also bound nearby, forming NADH and a carboxyl group from the aldehyde. Conservation of energy is maintained through this thioester linkage to the active site cysteine. The GAP intermediate is then used in the second step, where it is important to notice that without GAPDH's use of covalent catalysis, the energy barrier of the reaction would be too high and the reaction would be too slow for living organisms. Other roles: The importance of GAPDH in transcription was discovered by Zheng et. al. in 2003. It was found that OCA's transcriptional coactivator complex contains GAPDH, which moves between the cytosol and nucleus and may link the metabolic state to gene transcription. In 2005 the initiation of apoptosis was shown to be mediated by GAPDH by Hara et. al. when it was found to bind to DNA like it does in transcription activation. GAPDH was also found to be involved in ER to Golgi transport because it is recruited by rab2 to vesicular-tubular clusters of the endoplasmic reticulum where it helps form COP 1 vesicles. It was also found that GAPDH is plays a role in certain neruodegenerative disorders, as is able to find stretches which are encoded by the gene's CAG repeats and bind to the gene products formed from disorders such as Huntington's disease, Alzheimer’s disease, Parkinson’s disease and Machado-Joseph disease. Use in the lab: Quantitation: Overall, GAPDH is one of the most common “housekeeping genes” and is found in high levels in tissues and cells so it is commonly used in biological research as a loading control in quantification techniques such as Lowry Assays, Bradford Assays, Isoelectric Focusing, 2D-PAGE, Size Exclusion Chromatography (SEC), as well as 1-D and 2-D SDS-PAGE when it is conjugated to a known amount of biotin or BODIPY fluorophore to create a standard. A good method of quantitation lies under proteomics, which concompasses a variation of techniques including Differential in-gel Electrophoresis (DIGE), SILAC (for Metabolic Labeling), iTRAQ (for Chemical Labeling). Qualification and Analysis: Analysis of GAPDH can give much useful information when comparing proteins and substances in an experiment, thus some techniques used include Affinity Chromatography, Ion Exchange Chromatography, Reversed Phase LC. Often times in the lab, GAPDH from mouse cells is used. Spectroscopy can also be used to determine and compare make-up of the protein, with techniques including UV Spectroscopy, Circular Dichroism, Nuclear Magnetic Resonance (NMR), and Fluorescence. Further analysis in the lab can be done using Western blots and RT-PCR, but it has to be carefully controlled because under specific conditions it can have various regulation. Visualization and confirmation of important peptides is made possible by using one of a variey of Coomassie staining dyes-- most often Coomassie Brilliant Blue is used for western blots. Mass Spectrometry (MS) and MS/MS methods, used to determine the mass and elemental composition of particles, are also a useful technique to use. It has many variations including fast atom bombardment (FAB), thermospray, and direct analysis in real time (DART). For more specified experiments concentrating on specific parts of the protein, a variety of GAPDH ELISA kits have been used which utilize digestive enzymes such as Chymotrypsin and Trypsin to confirm the identity of the peptides. References ↑"GAPDH glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] - Gene - NCBI." National Center for Biotechnology Information. N.p., n.d. Web. 1 May 2012. ↑"Glyceraldehyde 3-phosphate dehydrogenase (EC 1." European Bioinformatics Institute | Homepage | EBI. N.p., n.d. Web. 1 May 2012. ↑"Glyceraldehyde 3-phosphate dehydrogenase - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 1 May 2012. ↑"Glyceraldehyde-3-phosphate Dehydrogenase." Biochemistry Dictionary. N.p., n.d. Web. 1 May 2012. ↑"Identification of tyrosine nitration in UCH‐L1 and GAPDH - Guingab‐Cagmat - 2011 - ELECTROPHORESIS - Wiley Online Library." Wiley Online Library. N.p., n.d. Web. 1 May 2012. ↑Isupov, M.N., and J.A. Littlechild. "Glyceraldehyde-3-phosphate Dehydrogenase." RCSB Protein Data Bank. N.p., 8 Oct. 1999. Web. 29 Apr. 2012. ↑Minter, Melissa. "Glyceraldehyde-3-phosphate Dehydrogenase." Oxidoreductases and the Reactions they Catalyze. N.p., n.d. Web. 20 Apr. 2012. ↑"Structure, Function, and Thermostability of GAPDH." GAPDH. N.p., n.d. Web. 28 Apr. 2012. ↑Watson, H.C., and J.C. Campbell. "Twinning In Crystals Of Human Skeletal Muscle D-Glyceraldehyde-3-Phosphate Dehydrogenase." RCSB Protein Data Bank. N.p., 27 Oct. 1983. Web. 28 Apr. 2012.