Cytoskeleton - University of Maryland College of Computer ... · PDF fileBiological functions...

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Cytoskeleton Made of proteins Dynamic properties Coordinate with each other Coordinate with external signal

Transcript of Cytoskeleton - University of Maryland College of Computer ... · PDF fileBiological functions...

Page 1: Cytoskeleton - University of Maryland College of Computer ... · PDF fileBiological functions of the cytoskeleton Tissue level Cell level Muscle movement Cell shape Cell movement Cell

CytoskeletonMade of proteinsDynamic propertiesCoordinate with each other Coordinate with external signal

Page 2: Cytoskeleton - University of Maryland College of Computer ... · PDF fileBiological functions of the cytoskeleton Tissue level Cell level Muscle movement Cell shape Cell movement Cell

Biological functions of the cytoskeleton

Tissue level Cell levelMuscle movement Cell shape

Cell movementCell adhesionMitosis

Subcellular levelIntracellular movement of vesiclesLocation of subcellular organellesOrganizing cell polarityEndocytosis – clathrin-mediated endocytosis and

phagocytosis

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Actin cytoskeleton

G-actin F-actinMg++

-

+

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Microtubule

Taxol

ExchangeableNon exchangeable

+ -

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Polymerization of G-actin

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0.6 μM 0.1 μM

Cc – Critical concentration

Treadmilling of actin filaments

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Assembly of microtubules

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Dynamic instability of microtubules

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Organization of the actin cytoskeleton

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Protein involved in the actin cytoskeleton

organization

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Regulation of actin

polymerization

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Figure 3. Dendritic Nucleation/Array Treadmilling Model for Protrusion of the Leading Edge(1) Extracellular signals activate receptors. (2) The associated signal transduction pathways produce active Rho-family GTPases and PIP2 that (3) activate WASp/Scar proteins. (4) WASp/Scar proteins bring together Arp2/3 complex and an actin monomer on the side of a preexisting filament to form a branch. (5) Rapid growth at the barbed end of the new branch (6) pushes the membrane forward. (7) Capping protein terminates growth within a second or two. (8) Filaments age by hydrolysis of ATP bound to each actin subunit (white subunits turn yellow) followed by dissociation of the γ phosphate (subunits turn red). (9) ADF/cofilin promotes phosphate dissociation, severs ADP-actinfilaments and promotes dissociation of ADP-actin from filament ends. (10)Profilin catalyzes the exchange of ADP for ATP (turning the subunits white), returning subunits to (11) the pool of ATP-actin bound to profilin, ready to elongate barbed ends as they become available. (12) Rho-family GTPases also activate PAK and LIM kinase, which phosphorylates ADF/cofilin. This tends to slow down the turnover of the filaments. (Redrawn from a figure in Pollard et al., 2000). Reprinted with permission from the Annual Review of Biophysics and Biomolecular Structure, Volume 29, copyright 2000 by Annual Reviews, www.annualreviews.org.

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Centrosome - a microtubule-organization center

C, centrioles; PC, pericentriolar matrix,

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Orientation of cellular microtubules

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γ-tubulin ring complex

The γ-tubulin ring complex is localized to one end of the microtubule

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Motors of the actin filaments

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Functions of myosin tail domains

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Kinesins (+) end-directed microtubule motors

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Kinesin-catalyzed vesicle transport

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Dynein (-) end-directed microtubule motors

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Actin-mediated cell migration

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Actin-mediated movement of Listeria in infected fibroblasts

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ER

microtubules

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Sperm Chlamydomonas

Flagella-mediated movement

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Cooperation of myosin and kinesin at cell cortex

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