File | Title | Manuscript Id |
Chapter Introduction | lodish8e_ch17_1.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_1_dlap.xml | 572b8d8b757a2e2232000000 |
17.1 Microfilaments and Actin Structures
| lodish8e_ch17_2.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_2_dlap.xml | 572b8d8b757a2e2232000000 |
Actin Is Ancient, Abundant, and Highly Conserved
| lodish8e_ch17_3.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_3_dlap.xml | 572b8d8b757a2e2232000000 |
G-Actin Monomers Assemble into Long, Helical F-Actin Polymers
| lodish8e_ch17_4.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_4_dlap.xml | 572b8d8b757a2e2232000000 |
F-Actin Has Structural and Functional Polarity
| lodish8e_ch17_5.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_5_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.1 | lodish8e_ch17_6.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_6_dlap.xml | 572b8d8b757a2e2232000000 |
17.2 Dynamics of Actin Filaments
| lodish8e_ch17_7.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_7_dlap.xml | 572b8d8b757a2e2232000000 |
Actin Polymerization In Vitro Proceeds in Three Steps
| lodish8e_ch17_8.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_8_dlap.xml | 572b8d8b757a2e2232000000 |
Actin Filaments Grow Faster at (+) Ends Than at (â) Ends
| lodish8e_ch17_9.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_9_dlap.xml | 572b8d8b757a2e2232000000 |
Actin Filament Treadmilling Is Accelerated by Profilin and Cofilin
| lodish8e_ch17_10.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_10_dlap.xml | 572b8d8b757a2e2232000000 |
Thymosin-β4 Provides a Reservoir of Actin for Polymerization
| lodish8e_ch17_11.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_11_dlap.xml | 572b8d8b757a2e2232000000 |
Capping Proteins Block Assembly and Disassembly at Actin Filament Ends
| lodish8e_ch17_12.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_12_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.2 | lodish8e_ch17_13.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_13_dlap.xml | 572b8d8b757a2e2232000000 |
17.3 Mechanisms of Actin Filament Assembly
| lodish8e_ch17_14.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_14_dlap.xml | 572b8d8b757a2e2232000000 |
Formins Assemble Unbranched Filaments
| lodish8e_ch17_15.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_15_dlap.xml | 572b8d8b757a2e2232000000 |
The Arp2/3 Complex Nucleates Branched Filament Assembly
| lodish8e_ch17_16.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_16_dlap.xml | 572b8d8b757a2e2232000000 |
Intracellular Movements Can Be Powered by Actin Polymerization
| lodish8e_ch17_17.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_17_dlap.xml | 572b8d8b757a2e2232000000 |
Microfilaments Function in Endocytosis
| lodish8e_ch17_18.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_18_dlap.xml | 572b8d8b757a2e2232000000 |
Toxins That Perturb the Pool of Actin Monomers Are Useful for Studying Actin Dynamics
| lodish8e_ch17_19.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_19_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.3 | lodish8e_ch17_20.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_20_dlap.xml | 572b8d8b757a2e2232000000 |
17.4 Organization of Actin-Based Cellular Structures
| lodish8e_ch17_21.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_21_dlap.xml | 572b8d8b757a2e2232000000 |
Cross-Linking Proteins Organize Actin Filaments into Bundles or Networks
| lodish8e_ch17_22.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_22_dlap.xml | 572b8d8b757a2e2232000000 |
Adapter Proteins Link Actin Filaments to Membranes
| lodish8e_ch17_23.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_23_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.4 | lodish8e_ch17_24.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_24_dlap.xml | 572b8d8b757a2e2232000000 |
17.5 Myosins: Actin-Based Motor Proteins
| lodish8e_ch17_25.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_25_dlap.xml | 572b8d8b757a2e2232000000 |
Myosins Have Head, Neck, and Tail Domains with Distinct Functions
| lodish8e_ch17_26.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_26_dlap.xml | 572b8d8b757a2e2232000000 |
Myosins Make Up a Large Family of Mechanochemical Motor Proteins
| lodish8e_ch17_27.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_27_dlap.xml | 572b8d8b757a2e2232000000 |
Conformational Changes in the Myosin Head Couple ATP Hydrolysis to Movement
| lodish8e_ch17_28.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_28_dlap.xml | 572b8d8b757a2e2232000000 |
Myosin Heads Take Discrete Steps Along Actin Filaments
| lodish8e_ch17_29.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_29_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.5 | lodish8e_ch17_30.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_30_dlap.xml | 572b8d8b757a2e2232000000 |
17.6 Myosin-Powered Movements
| lodish8e_ch17_31.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_31_dlap.xml | 572b8d8b757a2e2232000000 |
Myosin Thick Filaments and Actin Thin Filaments in Skeletal Muscle Slide Past Each Other During Contraction
| lodish8e_ch17_32.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_32_dlap.xml | 572b8d8b757a2e2232000000 |
Skeletal Muscle Is Structured by Stabilizing and Scaffolding Proteins
| lodish8e_ch17_33.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_33_dlap.xml | 572b8d8b757a2e2232000000 |
Contraction of Skeletal Muscle Is Regulated by Ca2+ and Actin-Binding Proteins
| lodish8e_ch17_34.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_34_dlap.xml | 572b8d8b757a2e2232000000 |
Actin and Myosin II Form Contractile Bundles in Nonmuscle Cells
| lodish8e_ch17_35.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_35_dlap.xml | 572b8d8b757a2e2232000000 |
Myosin-Dependent Mechanisms Regulate Contraction in Smooth Muscle and Nonmuscle Cells
| lodish8e_ch17_36.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_36_dlap.xml | 572b8d8b757a2e2232000000 |
Myosin VâBound Vesicles Are Carried Along Actin Filaments
| lodish8e_ch17_37.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_37_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.6 | lodish8e_ch17_38.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_38_dlap.xml | 572b8d8b757a2e2232000000 |
17.7 Cell Migration: Mechanism, Signaling, and Chemotaxis
| lodish8e_ch17_39.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_39_dlap.xml | 572b8d8b757a2e2232000000 |
Cell Migration Coordinates Force Generation with Cell Adhesion and Membrane Recycling
| lodish8e_ch17_40.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_40_dlap.xml | 572b8d8b757a2e2232000000 |
The Small GTP-Binding Proteins Cdc42, Rac, and Rho Control Actin Organization
| lodish8e_ch17_41.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_41_dlap.xml | 572b8d8b757a2e2232000000 |
Cell Migration Involves the Coordinate Regulation of Cdc42, Rac, and Rho
| lodish8e_ch17_42.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_42_dlap.xml | 572b8d8b757a2e2232000000 |
Migrating Cells Are Steered by Chemotactic Molecules
| lodish8e_ch17_43.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_43_dlap.xml | 572b8d8b757a2e2232000000 |
Key Concepts of Section 17.7 | lodish8e_ch17_44.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_44_dlap.xml | 572b8d8b757a2e2232000000 |
Key Terms
| lodish8e_ch17_45.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_45_dlap.xml | 572b8d8b757a2e2232000000 |
Review the Concepts
| lodish8e_ch17_46.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_46_dlap.xml | 572b8d8b757a2e2232000000 |
Extended References
| lodish8e_ch17_47.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_47_dlap.xml | 572b8d8b757a2e2232000000 |
Perspectives for the Future
| lodish8e_ch17_48.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_48_dlap.xml | 572b8d8b757a2e2232000000 |
Classic Experiment 17-1: Looking at Muscle Contraction | lodish8e_ch17_49.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_49_dlap.xml | 572b8d8b757a2e2232000000 |
Classic Experiment 17-2: Sensing Chemotactic Gradients | lodish8e_ch17_50.html | 572b8d8b757a2e2232000000 |
DLAP questions | lodish8e_ch17_50_dlap.xml | 572b8d8b757a2e2232000000 |