Skeletal muscle thin filament

Bacchiocchi, C., and Lehrer, S. S. (2002). Ca(2+) -induced movement of tropomyosin in skeletal muscle thin filaments observed by multi-site FRET. Biophys.J. 82,1524—1536. 

Schematic diagram of the organization of skeletal muscle thin filament, showing the position of tropo-myosin and the troponin complex on the actin filament. The binding of Ca " to TnC, the calcium-binding subunit of the troponin complex, removes Tnl, the inhibitory subunit, from actin and thus permits an interaction with a specialized protein, myosin, on neighboring thick muscle filaments (not shown). An ATP-driven conformation change in the myosin head group makes the thick and thin filaments move relative to one another, so that muscle contraction occurs.

The possible differences in on- and off-positions of tropomyosin in smooth and skeletal muscle thin filaments may relate to significant differences in enzymatic behavior of the two systems. The well-known observation that tropomyosin activates the smooth muscle actomyosin ATPase (Chacko et al., 1977) and also accelerates the motility of smooth muscle preparations in vitro (Shirinsky et al., 1992) should be taken into account when evaluating caldesmon function. Indeed, the degree of actomyosin ATPase potentiation by tropomyosin in the smooth muscle system is considerably greater than that in skeletal muscle preparations (Chacko et al., 1977 Sobieszek and Small, 1977 Chacko, 1981 Lehrer and Morris, 1984 Williams et al.,... 

The answer is b. (Murray, pp 48-62. Scriver, pp 3-45. Sack, pp 1-3. Wilson, pp 101-120.) Two kinds of interacting protein filaments are found in skeletal muscle. Thick filaments 15 nm in diameter contain primarily myosin. Thin filaments 7 nm in diameter are composed of actin, troponin, and tropomyosin. The thick and thin filaments slide past one another during muscle contraction. Myosin is an ATPase that binds to thin filaments during contraction, ot-actinin can be found in the Z line. 

Both smooth and skeletal muscle actin filaments are saturated with tropomyosin (Sobieszek and Bremel 1975). Both exhibit the same characteristic stoichiometry of binding of 1 molecule of tropomyosin interacting with 7 monomeric units of F-actin on each of the two strands of F-actin (Hartshorne 1987). The length of tropomyosin molecules (284 amino acids) and their periodicity in smooth and striated muscles is the same (Matsumura and Lin 1982). In both tissues, tropomyosin exists as a dimeric a-helical coil (Caspar et al 1969). Individual tropomyosin molecules bind in an end to end fashion to form a continuous strand on the thin filament that lies along the long-pitch of the double helix formed by the actin monomers (Moore et al 1970, OBrien et al 1971, Spudich et al 1972, Milligan et al 1990). 

Proteins can be broadly classified into fibrous and globular. Many fibrous proteins serve a stmctural role (11). CC-Keratin has been described. Fibroin, the primary protein in silk, has -sheets packed one on top of another. CoUagen, found in connective tissue, has a triple-hehcal stmcture. Other fibrous proteins have a motile function. Skeletal muscle fibers are made up of thick filaments consisting of the protein myosin, and thin filaments consisting of actin, troponin, and tropomyosin. Muscle contraction is achieved when these filaments sHde past each other. Microtubules and flagellin are proteins responsible for the motion of ciUa and bacterial dageUa. 

FIGURE 17.12 Electron micrograph of a skeletal muscle myofibril (in longitndinal section). The length of one sarcomere is indicated, as are the A and I bands, the H zone, the M disk, and the Z lines. Cross-sections from the H zone show a hexagonal array of thick filaments, whereas the I band cross-section shows a hexagonal array of thin filaments. (Photo courtesy of Hugh Huxley, Brandeis University)... 

The principal molecular constituent of thin filaments is actin. Actin has been highly conserved during the course of evolution and is present in all eukaryotes, including single-celled organisms such as yeasts. Actin was first extracted and purified from skeletal muscle, where it forms the thin filaments of sarcomeres. It also is the main contractile protein of smooth muscle. Refined techniques for the detection of small amounts of actin (e.g., immunofluorescence microscopy, gel electrophoresis, and EM cytochemistry) subsequently confirmed the presence of actin in a great variety of nonmuscle cells. Muscle and nonmuscle actins are encoded by different genes and are isoforms. 

Figure 1. Muscle development. A skeletal muscle fiber is formed by the fusion of many single cells (myoblasts) into a multinucleated myotube. Myotubes then develop into the muscle fiber (see text). Sarcomeres form in longitudinal structures called myofibrils. The repeating structure of the sarcomere contains interdigitating thick and thin filaments.

The myofibrils of skeletal muscle contain thick and thin filaments. The thick filaments contain myosin. The thin filaments contain actin, tropomyosin, and the troponin complex (troponins T, I, and C). 

Internally, muscle fibers are highly organized. Each fiber contains numerous myofibrils — cylindrical structures that also lie parallel to the long axis of the muscle. The myofibrils are composed of thick filaments and thin filaments. It is the arrangement of these filaments that creates alternating light and dark bands observed microscopically along the muscle fiber. Thus, skeletal muscle is also referred to as striated muscle. 

Actin filaments are the thinnest of the cytoskeletal filaments, and therefore also called microfilaments. Polymerized actin monomers form long, thin fibers of about 8 nm in diameter. Along with the above-mentioned function of the cytoskeleton, actin interacts with myosin ( thick ) filaments in skeletal muscle fibers to provide the force of muscular contraction. Actin/Myosin interactions also help produce cytoplasmic streaming in most cells. 

Contractile proteins which form the myofibrils are of two types myosin ( thick filaments each approximately 12 nm in diameter and 1.5 (im long) and actin ( thin filaments 6nm diameter and 1 (Am in length). These two proteins are found not only in muscle cells but widely throughout tissues being part of the cytoskeleton of all cell types. Filamentous actin (F-actin) is a polymer composed of two entwined chains each composed of globular actin (G-actin) monomers. Skeletal muscle F-actin has associated with it two accessory proteins, tropomyosin and troponin complex which are not found in smooth muscle, and which act to regulate the contraction cycle (Figure 7.1). 

Figure 1.12 Diagrammatic interpretation of contraction in a myo-fibril of skeletal muscle. The diagram shows a single sarcomere, the basic contractile unit, limited at each end by a Z-disc. Muscle fibres are packed with hundreds of parallel myofibrils, each of which consists of many, often thousands, of sarcomeres arranged end to end. Contraction is the conseguence of the thin actin filaments being pulled over the thick filaments to increase the region of overlap and telescope the sarcomere.

In skeletal muscle, actin is highly organised into filaments. The actin molecules, known as G-actins (each 42 kDa) form a pair, known as F-actin, which polymerise to form the thin filaments in the myofibrils (Figure 13.6). 

The striation of the muscle fibers is characteristic of skeletal muscle. It results from the regular arrangement of molecules of differing density. The repeating contractile units, the sarcomeres, are bounded by Z lines from which thin filaments of F-actin (see p. 204) extend on each side. In the A bands, there are also thick parallel filaments of myosin. The H bands in the middle of the A bands only contain myosin, while only actin is found on each size of the Z lines. 

The major allergen of molluscan shellfish is tropomyosin, a muscle protein. The term major allergen is used to define proteins that elicit IgE binding in the sera of half or more of patienfs wifh allergies to the specific source (Metcalfe et ah, 1996). Tropomyosin is a ubiquitous muscle protein in all animals. Tropomyosin is a 34- to 36-kDa protein that is highly water soluble and heat stable as evidenced by the fact that tropomyosin can be isolated from fhe water used to boil shrimp (Daul et ah, 1994). Tropomyosin can actually be found in bofh muscle and many nonmuscle cells in animals. In muscle cells, tropomyosin is associated with the thin filaments in muscle and plays a role in the contractile activity of muscle cells. In nonmuscle cells, tropomyosin is found in microfilaments but its fimction is less well imderstood. Tropomyosins are present in all eukaryotic cells. Different isoforms of tropomyosin are found in different types of muscle cells (skeletal, cardiac, smooth), brain, fibroblasts, and other nonmuscle cells. While these tropomyosins are highly homologous, small differences do exist in their... 

Figure 5.14 Schematic diagram showing interaction of thick and thin filaments in skeletal muscle contraction. (Adapted from Stryer, 1975.)...

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