Microtubules protein component

Until the past decade, the cytoplasm was widely considered to be structurally unorganized with the main division of labor at the organellar level. Certainly, relatively little was known about the nature of the cyto-skeleton (with the notable exception of the mitotic apparatus and striated muscle), and the dynamics of cytoplasmic behavior were conceptualized vaguely in terms of sol-gel transitions without a sound molecular foundation. Substantial improvements in electron, light, and fluorescence microscopy, as well as the isolation of discrete protein components of the cytoskeleton, have led the way to a much better appreciation of the structural organization of the cytoplasm. Indeed, the lacelike network of thin filaments, intermediate filaments, and microtubules in nonmuscle cells is as familiar today as the organelles identified... 

Intermediate filament a protein component of the cytoskeleton that includes filaments larger than the microfilaments and smaller than the microtubules. 

The cytoplasm of eukaryotic cells is traversed by three-dimensional scaffolding structures consisting of filaments (long protein fibers), which together form the cytoskeleton. These filaments are divided into three groups, based on their diameters microfilaments (6-8 nm), intermediate filaments (ca. 10 nm), and microtubules (ca. 25 nm). All of these filaments are polymers assembled from protein components. 

Electron microscopy (EM) has played a central role in many aspects of research on microtubules and their main protein component, tubulin. MTs were first identified in electron micrographs of plant material [1], Characteristics of the basic structural aspects of MTs were also determined by EM, revealing that MTs are hollow tubes composed of protofilaments (pf). There are most often 13 pfs, but this number can vary at least from 9 to 16. Subsequent work showed that the pfs are composed of aP-tubulin dimers arranged head-to-tail. 

The increase in nuclear cyclin B/CDKl activity promotes phosphorylation of nuclear substrates that are necessary for mitosis, such as nuclear envelope breakdown, spindle formation, chromatin condensation, and restmcturing of the Golgi and endoplasmic reticulum (85, 86). Numerous cyclin B/CDKl substrates have been dehned, which include nuclear lamins, nucleolar proteins, centrosomal proteins, components of the nuclear pore complex, and microtubule-associated proteins (87-89). Cyclin B/CDKl complexes also phosphorylate MCM4 to block replication of DNA, the TFIIH subunit of RNA polymerase II to inhibit transcription, and the ribosomal S6 protein kinase to prevent translation during mitosis (90-92). 

The structure of the cell, the shape of the cell surface, and the arrangement of subcellular organelles is organized by three major protein components microtubules composed of tubulin, which move and position organelles and vesicles thin filaments composed of actin, which form a cytoskeleton, and intermediate filaments composed of different fibrous proteins. Actin and tubulin, which are involved in cell movement, are dynamic structures composed of continuously associating and dissociating globular subunits. Intermediate filaments, which play a structural role, are composed of stable fibrous proteins that turn over more slowly. 

The question arises as to exactly how Ca +, cAMP, or both influence the functional form of microtubules. In partial answer to this question, Soifer et al. (1975) have demonstrated that a protein kinase resides as either a component part or in close association to the microtubule proteins. The protein kinase has as its most favorable substrate the protein tubulin itself, and therefore plays an important role in self-phos-phorylation of microtubules. Furthermore, cAMP increases the affinity of the enzyme for ATP and thereby increases self-phosphorylation two-to threefold, while 5 AMP inhibits the reaction. 

Certain proteins endow cells with unique capabilities for movement. Cell division, muscle contraction, and cell motility represent some of the ways in which cells execute motion. The contractile and motile proteins underlying these motions share a common property they are filamentous or polymerize to form filaments. Examples include actin and myosin, the filamentous proteins forming the contractile systems of cells, and tubulin, the major component of microtubules (the filaments involved in the mitotic spindle of cell division as well as in flagella and cilia). Another class of proteins involved in movement includes dynein and kinesin, so-called motor proteins that drive the movement of vesicles, granules, and organelles along microtubules serving as established cytoskeletal tracks. ... 

Even though dynein, kinesin, and myosin serve similar ATPase-dependent chemomechanical functions and have structural similarities, they do not appear to be related to each other in molecular terms. Their similarity lies in the overall shape of the molecule, which is composed of a pair of globular heads that bind microtubules and a fan-shaped tail piece (not present in myosin) that is suspected to carry the attachment site for membranous vesicles and other cytoplasmic components transported by MT. The cytoplasmic and axonemal dyneins are similar in structure (Hirokawa et al., 1989 Holzbaur and Vallee, 1994). Current studies on mutant phenotypes are likely to lead to a better understanding of the cellular roles of molecular motor proteins and their mechanisms of action (Endow and Titus, 1992). 

Thus far, microtubules and actin filaments and their associated proteins have been discussed to advantage as independent cytoskeletal components. In actual fact, all of the components of the cytoskeleton (including intermediate filaments) are precisely integrated with one another (Langford, 1995), as well as with various cytoplasmic organelles, the nuclear membrane, the plasma membrane, and the extracellular matrix. In its totality the cytoskeleton subserves many coordinated and regulated functions in the cell ... 

Gonc y We know of a requirement for astral microtubules, cytoplasmic dynein, the dynactin components p50and pi 50, as well as a protein called LET-99 (Hyman White 1987, Gonczy et al 1999b, Rose Kemphues 1998). 

Two of the cytoskeletal components, the actin filaments and the microtubules have been studied with molecular rotors. The main component of the actin filaments is the actin protein, a 44 kD molecule found in two forms within the cell the monomeric globulin form (G-actin) and the filament form (F-actin). Actin binds with ATP to form the microfilaments that are responsible for cell shape and motility. The rate of polymerization from the monomeric form plays a vital role in cell movement and signaling. Actin filaments form the cortical mesh that is the basis of the cytoskeleton. The cytoskeleton has an active relationship with the plasma membrane. Functional proteins found in both structures... 

This very brief overview provides only a glimpse of the complexity of microtubule systems, but the necessity to understand the underlying protein chemistry of microtubule components should be evident. 

There is also interest in the involvement of the cytoskeleton in such degenerative diseases as Alzheimer s disease (see Chapter 14) which is characterized by tangles (paired helical filaments). It seems likely that one of the microtubule-associated proteins (tau protein) is an important component of the tangles found in Alzheimer s disease. 

The principal cytoskeletal proteins in non-muscle cells are actin, tubulin, and the components of intermediate filaments. Actin can exist either as monomers ( G-actin ) or polymerized into 70 A diameter double filament ( F-actin ). Polymerized actin usually is localized at the margins of the cells, linked by other proteins to the cell membrane. In contrast, tubulin forms hollow filaments, approximately 250 A in diameter, that are distributed within a cell in association, generally, with cell organelles. Stabilized microtubule structures are found in the flagella and cilia of eucaryotic cells however, in other instances - examples being the mitotic apparatus and the cytoskeletal elements arising in directed cell locomotion - the microtubules are temporal entities. Intermediate filaments, which are composed of keratin-like proteins, are approximately 100 A thick and form stable structural elements that impart rigidity, for example, to nerve axons and epithelial cells. 

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