--Mark Hill 18:59, 12 May 2009 (EST) Your individual project (due week 10) is disappointing, in 8 weeks all you have managed is to identify the protein. Please insert any work at any draft stage you have carried out on your individual project before this week's lab.
--Mark Hill 08:33, 28 April 2009 (EST) Please see me ASAP You have not yet selected your individual project protein/method topic and still missing most homework items. 2009_Student#Individual_Projects Individual Projects I had previously left this message on your discussion page.
Necrosisis a type of cell death that is cause by cell injury, stress or ischemia. The underline mechanism of necrosis is complicated and it is mediated by certain proteins inside the cell. Calpain 1 and 2 are found to be essential to the necrosis, especially in the brain.
Calpains is a calcium-dependent proteases that is an intracellular protease that requires calcium for its catalytic activity.  Calpains exist ubiquitously in cells from humans to microorganisms. More than 10 different types of the calpain are reported in mammals. There are tho two ubiquitius isoforms of calpain, calpain 1 and calpain 2. These two form of calpains have different sensitivity to Ca2+: calpain 1 being activated at the micromolar Ca2+-concentration while calpain 2 at the millimolar Ca2+-concentration.  Studies suggest that calpain 1 and 2 activation in cell will lead to necrosis in the brain. It is initiated by the loss of Ca2+ homeostasis, which leads to calpain activation,cleavage of structural and regulatory proteins, and finally to necrotic neruron death.
Calpain 1 and calpain 2 comprise a highly homologous 80‐kDa large subunits and a common 30‐kDa small subunit. Both subunit together to from a heterodimer structure and containing multiple calcium-binding sites.    The 80 kDa subunit consists of four domains (I - IV) and the 30 kDa unit has 2 domains (V and VI).
- Domain I is actually not a romain and is removed during autolysis.
- Domain II is the protease domain, which is structurally similar to the catalytic domain of other cysteine proteases.
- Domain III exhibits a homology with typical calmodulin binding proteins and interacts with calcium binding domains IV.
- Domain IV is a Ca2+-binding domain similar to calmodulin.
- Domain V contains a N-terminal hydrophobic region and is essential for calpain interaction with membranes.
- Domain VI is C-terminal Ca2+ binding domain similar to domain IV and reported to have six EF-hands 
- cell adhesion: calpain cleaves the adhesion complex causing adhesion disassembly
- cell motility: calpain activation lead to tail retraction of the cells.
- cell spreading: calpain decrease the rate of cell spreading by decreasing proteolysis of adhesion complex proteins.
- cell death: The increase of intracellular CA2+ intiates the activation of calpain and causing necrosis.
Ischemic Neuronal death
Calpain contributes to the necrotic neuronal death in ischemia and neurodegeneration.  Yamashima T. reported that transient global brain ischemia which is a cause of delayed neuronal death of the vulnerable neurons is contributed by necrosis and apoptosis.  Calpain mainly play an role in the necrosis part.
After the ischemia of the neuron, there is an increase of Ca2+ concentration in the cell by the influx of the Ca2+ via several channesl in the cell and released by the ER. The raise in the intracellular [Ca2+] signal the activation of the calpain.   The activated calpain compromises the integrity of lysosomal membranes which lead to the disruption of the lysosomal membrane. The lysosomal membrane is a physical barrier that prevents hydrolytic enzymes from digesting the cell’s own cytoplasm. The rupture of the lysosomal membrane causes the leakage of the hydrolytic enzymes in to the cytoplasm which then digest the cell constituent proteins and finally to necrotic neuronal death. Cathepsin proteases is one of the enzymes released from the lysosome. So this is called "Calpain-cathepsin hypothesis"Actually, calpain is not killing the cell directly, its role is to mediate the activation of cathepsin that causes cytoskeletal degradation in the cell.
Calpastatin is an inhibitor of calpain which can prevent the activation of calpain in the cell.    However, the released of cathepsin from the lysosome mediates the activation of caspase. Caspase then induce the degradation of calpastatin. Finally the activation of calpain will be substained.
- Croall D. E. & Ersfeld K. (2007), The calpains: modular designs and functional diversity, Genome Biology 8:218-229 PMID 17608959
- Wang K. K. (2000), Calpain and caspase: can you tell the difference?, Trends in neucrosciences, 23(1): 20-26 PMID 10631785
- Sorimachi H, Ishiura S & Suzuki K. (1997), Structure and physiological function of calpains, The biochemical journal, 328(3): 721-732 PMID 9396712
- Croall D. E. and DeMartino G. N. (1991), Calcium-activated neutral protease (calpain) system: structure, function, and regulation, Physiological reviews, 71(3): 813-847 PMID 2057527
- Sorimachi H and Suzuki K. (2001), The structure of calpain., Journal of biochemistry, 129(5): 653-654 PMID 11328585
- Carafoli E., Molinari M. (1998), Calpain: a protease in search of a function?, Biochemical and biophysical communication, 247(2): 193-203 PMID 9642102
- Strobl S, Fernandez-Catalan C, Braun M, Huber R, Masumoto H, Nakagawa K et al. (2008), The crystal structure of calcium-free human m-calpain suggests an electrostatic switch mechanism for activation by calcium, PNAS, 97(2): 588-592 PMID 10639123
- Wells A., Huttenlocher A. & Lauffenburger D. A. (2005), Calpain Proteases in Cell Adhesion and Motility, International review of cytology, 245:1-16 PMID 16125543
- Franco S. J. and Huttenlocher A. (2005), Regulating cell migration: calpains make the cut, Journal of cell science, 118:3829-3838 PMID 16129881
- Syntichaki P., Xu K., Driscoll M.& Tavernarakis N.(2002), Specific aspartyl and calpain proteases are required for neurodegeneration in C. elegans, Nature, 419(6910): 939-944PMID 12410314
- Yamashima T. (2004), Ca2+-dependent proteases in ischemic neuronal death A conserved ‘calpain-cathepsin cascade’from nematodes to primates, Cell Calcium 36(3-4):285–293 PMID 15261484
- Syntichaki P, Tavernarakis N (2002),Death by necrosis. Uncontrollable catastrophe, or is there order behind the chaos?, EMOB Report, 3:7 604-609 PMID 12101090
What did you find interesting and did not know about the nucleus?
The 2 layers of membranes surrounding the necleus which are the outer membrane and the nuclear lamina. And there are intermediate filaments at the neclear lamina that i didn't know before. The membranes also contain pores for both passive and active passive. The concept of Chromosome Territories is so interesting, different chromsome occupying a specify region within the nucleus.
What did you find difficult to understand about exocytosis
The structures and functions oftThe 4 components involved in exocytosis is easy to understander. But I found that the concept of secretory vesicles is hard to understand and how does it related to membrane turnover?
What types of cellular processes require lots of energy from the mitochondria?
What do the acronyms (N-CAM) N-CAM, Ng-CAM L-CAM, I-CAM mean?
N-CAM -- Neural Cell Adhesion Molecule
Ng-CAM-- Neuron-glia cell adhesion molecule
L-CAM -- Liver CAM
I-CAM -- Intercellular adhesion molecule
What is the name of the epidermal layer between the basal and granulosa layer and how does it relate to intermediate filaments?
Stratum spinosum. It synthesizes a type of intermediate filament known as Cytokeratin, which are composed of keratin.
What are the 2 main forms of generating confocal microscopy?
Confocal laser scanning microscopes
Spinning-disk confocal microscopes
What does "S" stand for in the S phase?
S phase stand for "Synthesis"
--Mark Hill 18:34, 19 March 2009 (EST)You still need to provide feedback for Lecture 4 - Nucleus.