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Microtubules are a component of the cytoskeleton, found throughout the cytoplasm. These tubular polymers of tubulin can grow as long as 50 micrometres, with an average length of 25 µm, and are highly dynamic. The outer diameter of a microtubule is about 24 nm while the inner diameter is about 12 nm. They are found in eukaryotic cells and are formed by the polymerization of a dimer of two globular proteins, alpha and beta tubulin.
Microtubules are very important in a number of cellular processes. They are involved in maintaining the structure of the cell and, together with microfilaments and intermediate filaments, they form the cytoskeleton. They also make up the internal structure of cilia and flagella.They provide platforms for intracellular transport and are involved in a variety of cellular processes, including the movement of secretory vesicles, organelles, and intracellular substances (see entries for dynein and kinesin). They are also involved in cell division (mitosis and meiosis), including the formation of mitotic spindles, which are used to pull apart eukaryotic chromosomes.
Microtubules are nucleated and organized in microtubule organizing centres (MTOCs), such as the centrosome or the basal bodies found in cilia and flagella. These MTOCs may or may not possess centrioles.
There are many proteins that bind to microtubules, including motor proteins such as kinesin and dynein, severing proteins like katanin, and other proteins important for regulating microtubule dynamics.
The tubulin dimers polymerize end to end in protofilaments, which are the building-blocks for the microtubule structure. Thirteen protofilaments associate laterally to form a single microtubule and this structure can then extend by the addition of more protofilaments. In order for polymerization to occur, dimers must be present at a concentration above a specific minimum called the critical concentration, although the process is accelerated by the addition of nuclei, which are lengthened.
Microtubules have a distinct polarity that is important for their biological function. Tubulin polymerizes end to end, with the α-subunits of one tubulin dimer contacting the β-subunits of the next. Therefore, in a protofilament, one end will have the α-subunits exposed while the other end will have the β-subunits exposed. These ends are designated the (−) and (+) ends, respectively. The protofilaments bundle parallel to one another, so, in a microtubule, there is one end, the (+) end, with only β-subunits exposed, while the other end, the (−) end, has only α-subunits exposed. Elongation of microtubules typically only occurs from the (+) end.
The lateral association of the protofilaments generates an imperfect helix with one turn of the helix containing 13 tubulin dimers, each from a different protofilament. The image at the top of this article illustrates a small section of a microtubule, a few αβ dimers in length. The number of protofilaments can vary; microtubules made up of 14 protofilaments have been seen in vitro.
Microtubules are part of a structural network (the cytoskeleton) within the cell's cytoplasm. The primary role of the microtubule cytoskeleton is mechanical support, although microtubules also take part in many other processes. A microtubule is capable of growing and shrinking in order to generate force, and there are motor proteins that allow organelles and other cellular components to be carried along a microtubule. This combination of roles makes microtubules important for organizing cell layout.
Microtubules are typically nucleated and organized by dedicated organelles called microtubule-organizing centres (MTOCs). MTOCs associated with the base of a eukaryotic cilium or flagellum are typically termed basal bodies; otherwise MTOCs are called centrioles. In many cell types, microtubules are nucleated primarily at MTOCs; however, there are many exceptions to this rule.
Microtubules have a major structural role in eukaryotic cilia and flagella. Cilia and flagella always extend directly from a MTOC, in this case termed the basal body. The action of motor proteins on the various microtubule strands that run along a cilium or flagellum allows the organelle to bend and generate force for swimming, moving extracellular material, and other roles.
A notable structure involving microtubules is the mitotic spindle, used by most eukaryotic cells to segregate their chromosomes correctly during cell division. The mitotic spindle includes the spindle microtubules, microtubule-associated proteins (MAPs), and the MTOC. The microtubules originate in the MTOC and fan out into the cell; each cell has two MTOCs, as shown in the diagram.
The process of mitosis is facilitated by three main subgroups of microtubules, known as astral, polar, and kinetochore microtubules. An astral microtubule is a microtubule originating from the MTOC that does not connect to a chromosome. Astral microtubules instead interact with the cytoskeleton near the cell membrane and function in concert with specialized dynein motors, which pull the MTOC toward the cell membrane, thus assisting in correct positioning and orientation of the entire apparatus.
Kinetochore microtubules directly connect to the chromosomes, at the kinetochores. To clarify the terminology, each chromosome has two chromatids, and each chromatid has a kinetochore; the two kinetochores are linked. The complex created by the two kinetochores on a chromosome is called the centromere.
Polar microtubules extend from one MTOC and intertwine with the microtubules from the other MTOC; motor proteins then make them push against each other and assist in the separation of the two daughter cells.
Cell division in a typical eukaryote finishes with the generation of a final cytoplasmic bridge between the two daughter cells termed the midbody. This structure is built of microtubules that originally made up part of the mitotic spindle.
Microtubules are often nucleated at a dedicated microtubule-organizing center (MTOC). Contained within the MTOC is another type of tubulin, γ-tubulin, which is distinct from the α- and β-subunits, which compose the microtubules themselves. The γ-tubulin combines with several other associated proteins to form a circular structure known as the "γ-tubulin ring complex" (γ-TuRC). This complex acts as a scaffold for α/β-tubulin dimers to begin polymerization; it acts as a cap of the (−) end while microtubule growth continues away from the MTOC in the (+) direction.
Some cell types, such as plant cells, do not contain MTOCs. In these cells, microtubules are nucleated from discrete sites in the cytoplasm. Other cell types, such as trypanosomatid parasites, have a MTOC but it is permanently found at the base of a flagellum. Nucleation of microtubules for structural roles and for generation of the mitotic spindle is not from a canonical centriole-like MTOC. The regulation of the microtubule cytoskeleton in these cells is an intense area of study.
Dynamic instability refers to the coexistence of assembly and disassembly at the (+) end of a microtubule. The microtubule can dynamically switch between growing and shrinking phases in this region. During polymerization, both the α- and β-subunits of the tubulin dimer are bound to a molecule of GTP. The GTP bound to α-tubulin is stable and it plays a structural function in this bound state. However, the GTP bound to β-tubulin may be hydrolyzed to GDP shortly after assembly resulting in the addition of new dimers. The kinetics of GDP-tubulin are different from those of GTP-tubulin as GDP-tubulin is prone to depolymerization. A GDP-bound tubulin subunit at the tip of a microtubule will fall off, although a GDP-bound tubulin in the middle of a microtubule cannot spontaneously pop out. Since tubulin adds onto the end of the microtubule only in the GTP-bound state, there is a cap of GTP-bound tubulin at the tip of the microtubule, protecting it from disassembly. When hydrolysis catches up to the tip of the microtubule, it begins a rapid depolymerization and shrinkage. This switch from growth to shrinking is called a catastrophe. GTP-bound tubulin can begin adding to the tip of the microtubule again, providing a new cap and protecting the microtubule from shrinking. This is referred to as "rescue".
Microtubule plus ends are often localized to particular structures. As mentioned previously, they are found at kinetochores and used to pull chromosomes apart during mitosis. In polarized interphase cells, microtubules are disproportionately oriented from the MTOC toward the site of polarity, such as the leading edge of migrating fibroblasts. This configuration is thought to help deliver microtubule-bound vesicles from the Golgi to the site of polarity.
In 1986, Marc Kirschner and Tim Mitchison proposed that microtubules used their dynamic properties of growth and shrinkage at their plus ends to probe the three dimensional space of the cell. Plus ends that encounter kinetochores or sites of polarity become captured and no longer display growth or shrinkage. In contrast to normal dynamic microtubules, which have a half-life of 5–10 minutes, the captured microtubules can last for hours. This idea is commonly known as "the search and capture" model. Indeed, work since then has largely validated this idea. At the kinetochore, a variety of complexes have been shown to capture microtubule (+)-ends. Moreover, a (+)-end capping activity for interphase microtubules has also been described. This later activity is mediated by formins, the adenomatous polyposis coli protein, and EB1, a protein that tracks along the growing plus ends of microtubules.
The process of adding or removing monomers depends on the concentration of αβ-tubulin dimers in solution in relation to the critical concentration (Cc), which is the equilibrium constant for the dissociation of the dimers at the end of the microtubule.
The microtubule can, therefore, grow at both ends or only at one, depending on the concentrations of αβ-tubulin dimers. The interaction of the (-) end with MTOC will greatly decrease its activity.
These characteristics are derived from the existence of the microtubule’s dynamic instability, which means that in the same cell some microtubules are depolymerizing (catastrophe) and others are polymerizing (recovery).
“In vivo” microtubule dynamics vary considerably. Assembly, disassembly, and catastrophe rates depend on which microtubule-associated proteins (MAPs) are present. Classical MAPs are classified by their molecular weight into two groups:
They are also called τ(tau) proteins. They line the microtubule and form links with adjacent microtubules.
There are four known types of the heavier molecular weight MAPs: MAP-1, MAP-2, MAP-3 and MAP-4. MAP-1 proteins are a set of three different proteins: A, B and C. The C protein plays an important role in the retrograde transport of vesicles and is known as cytoplasmic dynein.
The MAP-4 proteins are found in the majority of cells and they stabilize the microtubules.
Besides the classic MAPs there are other MAP types:
A great number of drugs are able to bind to tubulin and modify its activation state. This will have the effect of interfering with microtubule dynamics. These drugs can have an effect at intracellular concentrations much lower than that of tubulin. This interference with microtubule dynamics can have the effect of stopping a cell’s cell cycle and can lead to programmed cell death or apoptosis. However there is data to suggest that interference of microtubule dynamics is insufficient to block the cells in mitosis. These studies have demonstrated that suppression of dynamics occurs at concentrations lower than those needed to block mitosis. Suppression of microtubule dynamics by tubulin mutation or by drug treatment inhibited cell migration.
Both microtubule stabilizers and destabilizers can suppress microtubule dynamics.
The drugs that can alter microtubule dynamics include:
Expression of β3-tubulin makes cells more aggressive by altering their response to drug-induced suppression of microtubule dynamics. In general the dynamics are normally suppressed by low, subtoxic concentrations of microtubule drugs that also inhibit cell migration. However, incorporating β3-tubulin into microtubules increases the concentration of drug that is needed to suppress dynamics and inhibit cell migration. Thus, tumors that express β3-tubulin are not only resistant to the cytotoxic effects of microtubule targeted drugs, but also to their ability to suppress tumor metastasis. Moreover, expression of β3-tubulin also counteracts the ability of these drugs to inhibit angiogenesis which is normally another important facet of their action.
Microtubule polymers are extremely sensitive to various environmental effects. Very low levels of free calcium can destabilize microtubules and this prevented early researchers from studying the polymer in vitro. Cold temperatures can also cause rapid depolymerization of microtubules.
Although most microtubules have a half-life of 5-10 min, certain microtubules can remain stable for hours. These stabilized microtubules accumulate post-translational modifications on their tubulin subunits by the action of microtubule-bound enzymes. However, once the microtubule depolymerizes, most of these modifications are rapidly reversed by soluble enzymes. Since most modification reactions are slow while their reverse reactions are rapid, modified tubulin is only detected on long-lived stable microtubules. Most of these modifications occur on the C-terminal region of alpha-tubulin. This region, which is rich in negatively charged glutamate, forms relative unstructured tails that stick out of the microtubule and form contacts with motors. Thus, it is believed that tubulin modifications regulate the interaction of motors with the microtubule. Since these stable modified microtubules are typically oriented towards the site of cell polarity in interphase cells, this subset of modified microtubules provide a specialized route that helps deliver vesicles to these polarized zones. These modifications include:
Tubulin is also known to be phosphorylated, ubiquitinated, sumoylated, and palmitoylated.
In addition to movement generated by the dynamic instability of the microtubule itself, the fibres are substrates along which motor proteins can move. Some proteins take advantage of the hydrolysis of ATP in order to generate mechanical energy and move substances along the microtubules. The major microtubule motor proteins are kinesin, which moves toward the (+) end of the microtubule, and dynein, which moves toward the (−) end.
Some viruses (including retroviruses, herpesviruses, parvoviruses, and adenoviruses) that require access to the nucleus to replicate their genomes attach to the motor proteins (dynein), which transport them at 1-4 μm/s to the centrosome, near the nucleus.
The cytoskeleton formed by microtubules is essential to the morphogenetic process of an organism’s development. For example, a network of whole, polarized microtubules is required to be present within the oocyte of Drosophila melanogaster during its embryogenesis in order to establish the axis of the egg. Signals sent between the follicular cells and the oocyte (such as factors similar to epidermal growth factor) cause the reorganization of the microtubules so that their (-) ends are located in the lower part of the oocyte, polarizing the structure and leading to the appearance of an anterior-posterior axis. This involvement in the body’s architecture is also seen in mammals.
Another area where microtubules are essential is the formation of the nervous system in higher vertebrates, where tubulin’s dynamics and those of the associated proteins (such as the MAPs) is finely controlled during the development of the brain's neuronal base.
The cellular cytoskeleton is a dynamic element that functions on many different levels: In addition to giving it a particular form and supporting the transport of vesicles and organelles, it can also influence gene expression. However, the signal transduction mechanisms involved in this communication are little understood. Notwithstanding this, the relationship between the drug-mediated depolymerization of microtubules and the specific expression of transcription factors has been described, which has provided information on the differential expression of the genes depending on the presence of these factors. This communication between the cytoskeleton and the regulation of the cellular response is also related to the generation of growth factors: for example, this relation exists for connective tissue growth factor.
This fact has a vital inconsistency in cancer treatments as paclitaxel (sold under the trademark taxol, a widely used antineoplastic drug) acts on cytoskeletal microtubules, and it is their interaction with elements that regulate the cell cycle that provokes, in the presence of antineoplastic drugs, a series of cellular failures in the cancerous cells that lead to planned cell death or apoptosis.
Recently, single microtubule is isolated and its electronic properties are measured using state of the art nano-probe technique, in an extremely noise free environment. Microtubule is electrical insulator (~300 mega Ohms), however, at particular ac frequencies, the dc conductivity decreases several orders of magnitude to a few kilohms. These frequencies are termed as electromagnetic resonance frequency. Sahu et al exhibited multi-level memory switching properties storing as much as ~500 bits, reversible switching like Random Access Memory (RAM) devices. Single molecule multi-level memory switching is an advanced atomic scale measurement technique, which exhibits massively parallel computing.
By controlled spectroscopic and microscopic measurement using Raman spectroscopy and Transmission Electron Microscopy(TEM) it is demonstrated that the ripples of energy flowing through tubulin proteins condense into a few vibrational peaks, the energy condensation into Raman peaks is abundant in several materials, but not in many biomaterials. Most importantly the coherent oscillations observed in TEM disappears, as soon as the water channel is taken out from single microtubule core.
Complete resonance band or all ac frequencies at which there is a substantial decrease in the electrical resistance of the single tubulin protein molecule and single microtubule molecule has been determined. Here we copy the resonance frequencies from the published manuscript. A single Tubulin acts just like a single molecule oscillator, has three resonance bands (10^7 ~ 10^13 Hz, gap in order ~6) Triplet 1 (80–140 MHz, 180–250 MHz, 300–400 MHz); Triplet 2 (12–18 GHz, 25–50 GHz, 100–300 GHz), Triplet 3 (2–20 THz, 22–30 THz, 35–60 THz). Here 5-15THz is inaccessible THz band, wherein for a long time we had a technological gap. A single microtubule, acts just like a single molecule oscillator, the frequency ranges of three resonance bands are (10^4 ~ 10^10 Hz, gap in order ~6) Triplet 1 (15–20 kHz, 25–80 kHz, 100–300 kHz), Triplet 2 (10–19 MHz, 20–40 MHz, 100–228 MHz), Triplet 3 (1–5 GHz, 7–10 GHz, 15–30 GHz).
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