Microfilament
Microfilaments, also called actin filaments, are
Actin was first discovered in rabbit skeletal muscle in the mid 1940 by F.B. Straub.[3] Almost 20 years later, H.E. Huxley demonstrated that actin is essential for muscle constriction. The mechanism in which actin creates long filaments was first described in the mid 1980. Later studies showed that actin has an important role in cell shape, motility, and cytokinesis.
Organization
Actin filaments are assembled in two general types of structures: bundles and networks. Bundles can be composed of polar filament arrays, in which all barbed ends point to the same end of the bundle, or non-polar arrays, where the barbed ends point towards both ends. A class of actin-binding proteins, called cross-linking proteins, dictate the formation of these structures. Cross-linking proteins determine filament orientation and spacing in the bundles and networks. These structures are regulated by many other classes of actin-binding proteins, including motor proteins, branching proteins, severing proteins, polymerization promoters, and capping proteins.
In vitro self-assembly
Measuring approximately 6
In vitro actin polymerization, or
Subsequently,
Actin polymerization together with capping proteins were recently used to control the 3-dimensional growth of protein filament so as to perform 3D topologies useful in technology and the making of electrical interconnect. Electrical conductivity is obtained by metallisation of the protein 3D structure.[6][7]
Mechanism of force generation
As a result of ATP hydrolysis, filaments elongate approximately 10 times faster at their barbed ends than their pointed ends. At
Actin in cells
Intracellular actin cytoskeletal assembly and disassembly are tightly regulated by cell signaling mechanisms. Many signal transduction systems use the actin cytoskeleton as a scaffold, holding them at or near the inner face of the peripheral membrane. This subcellular location allows immediate responsiveness to transmembrane receptor action and the resulting cascade of signal-processing enzymes.
Because actin monomers must be recycled to sustain high rates of actin-based motility during
Another important component in filament formation is the Arp2/3 complex, which binds to the side of an already existing filament (or "mother filament"), where it nucleates the formation of a new daughter filament at a 70 degree angle relative to the mother filament, effecting a fan-like branched filament network.[8]
Specialized unique actin cytoskeletal structures are found adjacent to the plasma membrane. Four remarkable examples include
Associated proteins
In non-muscle cells, actin filaments are formed proximal to membrane surfaces. Their formation and turnover are regulated by many proteins, including:
- Filament end-tracking protein (e.g., N-WASP)
- Filament-nucleator known as the Actin-Related Protein-2/3 (or Arp2/3) complex
- Filament cross-linkers (e.g., α-actinin, fascin, and fimbrin)
- Actin monomer-binding proteins profilin and thymosin β4
- Filament barbed-end cappers such as Capping Protein and CapG, etc.
- Filament-severing proteins like gelsolin.
- Actin depolymerizing proteins such as ADF/cofilin.
The actin filament network in non-muscle cells is highly dynamic. The actin filament network is arranged with the barbed-end of each filament attached to the cell's peripheral membrane by means of clamped-filament elongation motors, the above-mentioned "actoclampins", formed from a filament barbed-end and a clamping protein (formins, VASP, Mena, WASP, and N-WASP).[15] The primary substrate for these elongation motors is profilin-actin-ATP complex which is directly transferred to elongating filament ends.[16] The pointed-end of each filament is oriented toward the cell's interior. In the case of lamellipodial growth, the Arp2/3 complex generates a branched network, and in filopodia a parallel array of filaments is formed.
Actin acts as a track for myosin motor motility
Myosin motors are intracellular ATP-dependent enzymes that bind to and move along actin filaments. Various classes of myosin motors have very different behaviors, including exerting tension in the cell and transporting cargo vesicles.
A proposed model – actoclampins track filament ends
One proposed model suggests the existence of actin filament barbed-end-tracking molecular motors termed "actoclampin".
The term actoclampin is derived from acto- to indicate the involvement of an actin filament, as in actomyosin, and clamp to indicate a clasping device used for strengthening flexible/moving objects and for securely fastening two or more components, followed by the suffix -in to indicate its protein origin. An actin filament end-tracking protein may thus be termed a clampin.
Dickinson and Purich recognized that prompt ATP hydrolysis could explain the forces achieved during actin-based motility.[15] They proposed a simple mechanoenzymatic sequence known as the Lock, Load & Fire Model, in which an end-tracking protein remains tightly bound ("locked" or clamped) onto the end of one sub-filament of the double-stranded actin filament. After binding to Glycyl-Prolyl-Prolyl-Prolyl-Prolyl-Prolyl-registers on tracker proteins, Profilin-ATP-actin is delivered ("loaded") to the unclamped end of the other sub-filament, whereupon ATP within the already clamped terminal subunit of the other subfragment is hydrolyzed ("fired"), providing the energy needed to release that arm of the end-tracker, which then can bind another Profilin-ATP-actin to begin a new monomer-addition round.[citation needed]
Steps involved
The following steps describe one force-generating cycle of an actoclampin molecular motor:
- The polymerization cofactor profilin and the ATP·actin combine to form a profilin-ATP-actin complex that then binds to the end-tracking unit
- The cofactor and monomer are transferred to the barbed-end of an actin already clamped filament
- The tracking unit and cofactor dissociate from the adjacent protofilament, in a step that can be facilitated by ATP hydrolysis energy to modulate the affinity of the cofactor and/or the tracking unit for the filament; and this mechanoenzymatic cycle is then repeated, starting this time on the other sub-filament growth site.[citation needed]
When operating with the benefit of ATP hydrolysis, AC motors generate per-filament forces of 8–9 pN, which is far greater than the per-filament limit of 1–2 pN for motors operating without ATP hydrolysis.[15][17][18] The term actoclampin is generic and applies to all actin filament end-tracking molecular motors, irrespective of whether they are driven actively by an ATP-activated mechanism or passively.
Some actoclampins (e.g., those involving Ena/VASP proteins, WASP, and N-WASP) apparently require Arp2/3-mediated filament initiation to form the
References
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- ^ ISBN 978-1-4160-2388-3.
- PMID 23396247.
- ^ US Patent US 9070702, Method for obtaining three-dimensional actin structures and uses thereof, Jean-Christophe Gabriel, Laurent Blanchoin, Manuel Thery, Remi Galland
- PMID 9600938.
- PMID 27055045.
- PMID 28690919.
- PMID 23239625.
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- ^ PMID 17056726.
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- ^ PMID 15454475.
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External links
- Microfilaments at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- Microfilament+proteins at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- "Microfilament" at Dorland's Medical Dictionary