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Lecture 16 Outline
Lecture 16 Outline

... Functions in Maintenance of Cell Shape (tension bearing elements)changes in Cell Shape, Muscle Contraction, Cell Motility (Pseudopodia), Cell Division (Cleavage Furrow Formation) Actin Filaments have polarity, bind ATP, hydrolysis reduces affinity of monomers for each other- reducing polymer stabili ...
Actin - WordPress.com
Actin - WordPress.com

... o Monomers add to both ends, but add faster at the + end. o The Hydrolysis of ATP is slow. What happens when a low concentration of ATP is bound to G-Actin? o Treadmilling can occur if it is not too low. This is where monomers add to + end and come off of the – end at the same rate, causing the leng ...
Sequence of Events in Muscular Contraction
Sequence of Events in Muscular Contraction

... The following is a list of the main events in muscular contraction and relaxation. The sequence begins with the initiation of an action potential by the motor nerve. This impulse is propagated over the entire surface of the muscle fiber as the cell membrane becomes depolarized. 1. Depolarization of ...
Multivalent cross-linking of actin filaments and microtubules through
Multivalent cross-linking of actin filaments and microtubules through

... and cross-link actin filaments with microtubules. In addition, aberrant interaction of the microtubule-associated protein Tau with filamentous actin is connected to synaptic impairment in Alzheimer’s disease. Here we provide insight into the nature of interaction between actin filaments and microtub ...
Contractile Proteins - Mrs. DeNicola's Science Corner
Contractile Proteins - Mrs. DeNicola's Science Corner

... -Contractile proteins are the force generators of muscle contraction -They are part of what makes up our muscle fibers, along with regulatory and structural proteins -The types of contractile proteins that are in muscle fibers are actin, which is part of thin filament, and myosin, which is part of t ...
Slide 1
Slide 1

... How do Molecules form Living, Moving, Reproducing Cells? 1683, Leeuwenhoek: “An unbelievably great company of living animalcules, a-swimming more nimbly than any I had ever seen up to this time. The biggest sort bent their body into curves in going forwards." ...
A Figure S7. A. Standard curve of actin quantification using silver
A Figure S7. A. Standard curve of actin quantification using silver

... 75 kDa Actin in supernatant 42 kDa ...
UPenn_MRSEC_1120901_SEED4_Discher_Lipid
UPenn_MRSEC_1120901_SEED4_Discher_Lipid

... ...
< 1 ... 5 6 7 8 9

Actin



Actin is a globular multi-functional protein that forms microfilaments. It is found in essentially all eukaryotic cells (the only known exception being nematode sperm), where it may be present at concentrations of over 100 μM. An actin protein's mass is roughly 42-kDa and it is the monomeric subunit of two types of filaments in cells: microfilaments, one of the three major components of the cytoskeleton, and thin filaments, part of the contractile apparatus in muscle cells. It can be present as either a free monomer called G-actin (globular) or as part of a linear polymer microfilament called F-actin (filamentous), both of which are essential for such important cellular functions as the mobility and contraction of cells during cell division.Actin participates in many important cellular processes, including muscle contraction, cell motility, cell division and cytokinesis, vesicle and organelle movement, cell signaling, and the establishment and maintenance of cell junctions and cell shape. Many of these processes are mediated by extensive and intimate interactions of actin with cellular membranes. In vertebrates, three main groups of actin isoforms, alpha, beta, and gamma have been identified. The alpha actins, found in muscle tissues, are a major constituent of the contractile apparatus. The beta and gamma actins coexist in most cell types as components of the cytoskeleton, and as mediators of internal cell motility. It is believed that the diverse range of structures formed by actin enabling it to fulfill such a large range of functions is regulated through the binding of tropomyosin along the filaments.A cell’s ability to dynamically form microfilaments provides the scaffolding that allows it to rapidly remodel itself in response to its environment or to the organism’s internal signals, for example, to increase cell membrane absorption or increase cell adhesion in order to form cell tissue. Other enzymes or organelles such as cilia can be anchored to this scaffolding in order to control the deformation of the external cell membrane, which allows endocytosis and cytokinesis. It can also produce movement either by itself or with the help of molecular motors. Actin therefore contributes to processes such as the intracellular transport of vesicles and organelles as well as muscular contraction and cellular migration. It therefore plays an important role in embryogenesis, the healing of wounds and the invasivity of cancer cells. The evolutionary origin of actin can be traced to prokaryotic cells, which have equivalent proteins. Actin homologs from prokaryotes and archea polymerize into different helical or linear filaments consisting of one or multiple strands. However the in-strand contacts and nucleotide binding sites are preserved in prokaryotes and in archea. Lastly, actin plays an important role in the control of gene expression.A large number of illnesses and diseases are caused by mutations in alleles of the genes that regulate the production of actin or of its associated proteins. The production of actin is also key to the process of infection by some pathogenic microorganisms. Mutations in the different genes that regulate actin production in humans can cause muscular diseases, variations in the size and function of the heart as well as deafness. The make-up of the cytoskeleton is also related to the pathogenicity of intracellular bacteria and viruses, particularly in the processes related to evading the actions of the immune system.
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