BME Engineering Molecular Cell Biology. The Cytoskeleton (I): Actin The Cytoskeleton (II): Microtubule & Intermediate Filament

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BME 42-620 Engineering Molecular Cell Biology Lecture 09: The Cytoskeleton (I): Actin The Cytoskeleton (II): Microtubule & Intermediate Filament BME42-620 Lecture 09, September 27, 2011 1

Outline Overviewofcytoskeletal filaments Actin and its associated proteins Microtubule and its associated proteins; Centrosome Intermediate filament and its associated proteins 2

Outline Overviewofcytoskeletal filaments Actin and its associated proteins Microtubule and its associated proteins; Centrosome Intermediate filament and its associated proteins 3

The Cytoskeleton is Highly Dynamic and Regulated 4

Overview of Cytoskeletal Filaments Shape Diameter Subunits Polarized actin cable ~6 nm actin monomer microtubule tube ~25nm tubulin heterodimer intermediate filament rope ~10nm Various dimers yes yes no 5

Catalyzed and Regulated Self-Assembly of Macromolecules (I) Binding specificity between monomers is determined by multiple weak bonds on complementary surfaces. Demo: poliovirus capsid self assembly Olson, A. J., Hu, Y. H. E., & Keinan, E. (2007). Chemical mimicry of viral capsid self-assembly. Proceedings of the National Academy of Sciences, 104(52), 20731-20736. 6

Catalyzed and Regulated Self-Assembly of Macromolecules (II) Cellular macromolecules often form through self-assembly of small subunits. This process requires energy and is often catalyzed and regulated. Advantages: - Reduced possibility of error - Possibility for repair - Subunit can be recycled - Assembly provides multiple entry points for regulation - Regulation of subunit synthesis and degradation - Regulation of nucleation - Regulation by changing environmental conditions - Regulation by modifying subunits - Regulation using accessory proteins 7

Example: Self-Assembly of a Tobacco Mosaic Virus The virus is made of 2130 protein subunits of 158 amino acids each. It also has a single-stranded RNA of 6390 nucleotids. Translation error 1 out of 3000 amino acids (0.99967) Probability of making a correct TMV = 0.99967 158 =0.949 If instead the TMV is assembled from one large sequence of amino acid, probability of making a correct TMV = 0.99967 336540 =1.87X10-49 Self-assembly is one of the central principles in biology. The assembly information is encoded in weak but highly specific noncovalent interactions. Pollard & Earnshaw, Cell Biology, 2/e, 2008, Chapter 5, 8

ATP (adenosine triphosphate) p )() (I) ATP is the most widely used energy carrier in cells. 9

ATP (adenosine triphosphate) p )(II) Synthesis of biological polymers is driven by ATP hydrolysis. 10

Outline Overviewofcytoskeletal filaments Actin and its associated proteins Microtubule and its associated proteins; Centrosome Intermediate filament and its associated proteins 11

Organization of Actin with a Cell 12

Actin Structure and Function Each actin subunit is a globular monomer. One ATP binding site per monomer. Functions - Cell migration - Cell shape - Used as tracks for myosin for short distance transport Pollard & Cooper, Science,326-1208, 2009 13

Basics Terms of Chemical Reaction Kinetics A reversible bimolecular binding reaction A + B AB Rate of association = k + [A][B] Rate of disassociation = k - [AB] At equilibrium k + [A][B] = k - [AB] 14

Actin Nucleation and Nucleotide Hydrolysis Actin polymerizes and depolymerizes substantially faster at tthe plus end d(barbed b end) d)than at the minus end (pointed end). 15

Actin Associated Proteins (I) More than 100 associated proteins identified so far. Functions - Monomer binding - Nucleation - Filament capping - Filament severing - Filament side-binding and supporting - Filament crosslinking -Signaling g adapter Functional overlap and collaboration between actin- binding proteins 16

17

Actin Associated Proteins (II) Monomer binding proteins - profilin: to bind actin monomer and accelerate elongation - thymosin: to bind and lock actin monomer - ADF/cofilin: to bind and destabilize ADP-actin filaments 18

Actin Associated Proteins (III) Actin nucleation - Formins: to initiate unbranched actin filaments - Arp2/3: to bind the side of actin and initiate branching 19

Actin Associated Proteins (IV) Actin capping protein - Blocks subunit association and disassociation Actin severing protein Three families of proteins perform both functions - Gelsolin - Fragmin-severin - ADF/cofilin 20

Actin Associated Proteins (V) Actin side-binding proteins tropomyosin, nebulin, caldesmon Actin crosslinking protein - -actinin - filamin - spectrin -ERM 21

Actin Adapter Protein Adaptor proteins such as WASP (a branching mediating factor) & VASP (a polymerization mediating factor) server as connectors between signaling pathways and actin assembly. WASP: Wiskott-Aldrich syndrome protein 22

Actin Regulation GTPase: Molecule switch; Family of enzymes that are activated by GTP binding and inactivated by GTP hydrolysis and phosphate dissociation. GTPases: cdc42: its activation triggers actin polymerization and bundling at filopodia. Rho: its activation promotes actin bundling. Rac: its activation promotes polymerization at the cell periphery. 23

GTP (guanosine triphosphate) GTP-binding proteins (GTPases) are important signaling molecules. When GTP is hydrolyzed into GDP, the GTP binding domain undergoes a conformation change that inactivates the GTPase. 24

Rac on Actin Organization 25

Summary: actin Relatively soft (quantification to follow in later lectures). Often form bundles; mechanical strength comes mostly from bundling and crosslinking. Mostly function to withstand tension rather than compression. Relatively stable and easy to work with (biochemically). 26

Summary: actin associated proteins Different associated proteins serve a broad range of functions. Proteins with multiple functional domains can have multiple functions. Some but not all of them are essential. Most of the proteins have functional overlap. 27

Outline Overviewofcytoskeletal filaments Actin and its associated proteins Microtubule and its associated proteins; Centrosome Intermediate filament and its associated proteins 28

Microtubule Structure Polarized -plus ( -tubulin) end - minus ( -tubulin) end Outer diameter: 25 nm Typically y 13 protofilaments; Some have 11, 15, 16, etc 29

Microtubule Organization During interphase - Radial pattern organized around the centrosome During metaphase - Bipolar architecture t Fig. 34-1 30

Microtubule Dynamic Instability 31

Microtubule Dynamic Instability T. Wittmann et al, J. Cell Biol., 161:845, 2003. 32

Microtubule Dynamic Instability Parameters Kinoshita et al, Science, 294:1340, 2001 33

34

Microtubule Associated Proteins (I) Stabilizing MAPs Tau Binds side and stabilizes microtubules MAP2, MAP4 Binds side and stabilizes microtubules Destabilizing MAPs Op18/stathmin Binds tubulin dimers & destabilizes MTs Katanin AAA ATPase that severs microtubules XKCM/MCAK Kinesin-related; destabilizes plus ends 35

Electron Microscopy of Microtubules Decorated with MAPs Frozen deep-etched, shadowed microtubules with (upper) and without (lower) tau Fixed, embedded sections of microtubules with (upper) and without (lower) MAP2 Fig. 34-11

Microtubule Associated Proteins (II) Plus end track protein CLIP170 EB1 Links membranes to growing plus ends Links APC to MT plus ends Dynamics and mechanics of the microtubule plus end. Howard J, Hyman AA. Nature. 2003 422(6933):753-8. 37

Summary: Microtubule Relatively rigid (quantification in following lectures). Often form bundles; mechanical strength comes mostly from bundling and crosslinking. Can withstand compression. Can denature easily; Difficult to work with (biochemically). 38

Centrosome 39

Outline Overviewofcytoskeletal filaments Actin and its associated proteins Microtubule and its associated proteins; Centrosome Intermediate filament and its associated proteins 40

Intermediate Filament So named because of its diameter in striated muscles (diameter ~10nm). Its core structure is an -helical coiled coil. N- and C-terminal domains vary considerably in size. 41

Intermediate Filament Classification 42

Intermediate Filament Biochemically most stable among the three filaments Assembly disassembly regulated by phosphorylation - Phosphorylation: reaction in which a phosphate group is covalently coupled to another molecule. - Kinase: an enzyme that catalyzes the addition of phosphate groups - Phosphatase: an enzyme that catalyzes the removal of phosphate groups Phosphorylation may stabilize or destabilize intermediate filaments. 43

Intermediate Filament Associated Proteins 44

Plectin Connects IFs to Actin & Microtubules 45

Flexible but stable. Intermediate Filaments Primary assumed function is to prevent excessive stretching. In general, much less is known about intermediate t filaments 46

An Example: Microtubule, Intermediate Filament & Organelles in a Frog Axon N. Hirokawa, J. Cell Biol. 94:129, 1982 Nobutaka Hirokawa University of Tokyo Bar: 0.1 m 47

Required Reading Chapters 2 & 16 48

Questions? 49