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Generation of Straight or Branched Actin Filaments01:14

Generation of Straight or Branched Actin Filaments

The straight or branched structure formation of actin filaments is controlled by nucleating proteins such as the formins and Arp2/3 complex. Formin-mediated assembly results in straight filaments, whereas Arp2/3 protein complex-mediated assembly results in branched actin filaments.
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...
Actin Polymerization01:42

Actin Polymerization

Actin polymerization occurs through the head-to-tail association of binding sites on monomeric actin or G-actin to form filamentous or F-actin. The polymerization can be divided into three phases ̶  nucleation, elongation, and steady-state phase.
The nucleation phase involves forming a stable nucleus consisting of three actin monomers to form a new actin filament. Actin-binding proteins such as formins and Arp2/3 complex help filament growth post-nucleation. The Formins form straight actin...
Mechanism of Filopodia Formation01:39

Mechanism of Filopodia Formation

Filopodia are thin, actin-rich cellular protrusions that play an important role in many fundamental cellular functions. They vary in their occurrence, length, and positioning in different cell types, suggesting their diverse roles.
Their main function is to guide migrating cells during normal tissue morphogenesis or cancer metastasis by recognizing and making initial contacts with the extracellular matrix. However, they can also act as stationary cell anchors or help to establish communication...
Actin Filament Depolymerization01:19

Actin Filament Depolymerization

Actin filaments (F-actin) are composed of actin subunits. The dissociation of actin monomers can occur from either end of F-actin. The rate of dissociation is faster from the minus-end or the pointed end, where the actin subunits exist with a bound ADP, together known as ADP-actin. The depolymerization of F-actin is aided by proteins, including the actin-depolymerizing factor (ADF) and cofilin family of proteins, gelsolin, and glia maturation factor (GMF).
In F-actin, the ADF/cofilin proteins...
Formation of Higher-order Actin Filaments01:11

Formation of Higher-order Actin Filaments

The polymerization of G-actin monomers into filamentous F-actin is a multi-step process. Once the F-actins are formed, they can bundle together in different arrangements to form higher-order networks and regulate cellular functions. Common examples include the formation of lamellipodia and filopodia at the cell's leading edge by actin reorganization in a migrating cell. The microvilli on the brush border epithelial cells are also formed through the F-actin network.
The high-order actin networks...
Introduction to Actin01:26

Introduction to Actin

Actin is a highly conserved cytoskeletal protein found abundantly in eukaryotic cells. It constitutes 10% weight of the total cellular protein in muscle cells, while in non-muscle cells, it is lower and makes up around 1–5 percent of the total cell protein. Actin found in the unicellular amoebae and complex multicellular animals is around 80% similar, demonstrating their conservation over a billion years of evolution.  Actin coding genes are conserved within species and across different species.

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Related Experiment Video

Updated: May 24, 2026

Reconstitution of Actin-Based Motility with Commercially Available Proteins
08:40

Reconstitution of Actin-Based Motility with Commercially Available Proteins

Published on: October 28, 2022

Structural basis for profilin-mediated actin nucleotide exchange.

Jason C Porta1, Gloria E O Borgstahl

  • 1Department of Biochemistry and Molecular Biology, 987696 Nebraska Medical Center, Omaha, NE 68198-7696, USA.

Journal of Molecular Biology
|February 28, 2012
PubMed
Summary
This summary is machine-generated.

Mammalian profilin binding to actin filaments facilitates ATP exchange, crucial for cell motility and division. Crystal structures reveal how profilin binding induces conformational changes, enabling nucleotide exchange and filament growth.

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Using Microfluidics and Fluorescence Microscopy to Study the Assembly Dynamics of Single Actin Filaments and Bundles
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Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence (TIRF) Microscopy
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Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence (TIRF) Microscopy

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Reconstitution of Actin-Based Motility with Commercially Available Proteins
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Using Microfluidics and Fluorescence Microscopy to Study the Assembly Dynamics of Single Actin Filaments and Bundles
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Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence (TIRF) Microscopy
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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Background:

  • Actin is a key eukaryotic protein essential for cellular structure, movement, and division.
  • Actin filament formation relies on the exchange of actin-bound ADP for ATP.
  • Profilin is a mammalian protein that binds actin and catalyzes nucleotide exchange.

Purpose of the Study:

  • To elucidate the structural mechanism by which profilin facilitates nucleotide exchange on actin.
  • To understand the conformational changes in actin upon profilin binding.

Main Methods:

  • X-ray crystallography of profilin-actin complexes.
  • Structural analysis of protein-protein interactions and conformational changes.

Main Results:

  • Crystal structures revealed profilin-bound actin with actively exchanging ATP.
  • Profilin binding induces a rotation of actin's small domain relative to its large domain.
  • This rotation shifts nucleotide loops, repositions calcium ions, and closes the ATP-binding cleft, involving Trp356.

Conclusions:

  • Profilin binding to actin triggers specific conformational changes that promote ATP/ADP exchange.
  • The structural insights explain profilin's role in regulating actin dynamics.
  • Secondary calcium binding sites were also identified, suggesting additional regulatory roles.