Troponin is a complex of three regulatory proteins that is integral to
muscle contraction in
skeletal and
cardiac muscle, but not
smooth muscle. Troponin is attached to the protein
tropomyosin and lies within the groove between
actin filaments in muscle tissue. In a relaxed muscle, tropomyosin blocks the attachment site for the
myosin crossbridge, thus preventing contraction. When the muscle cell is stimulated to contract by an
action potential,
calcium channels open in the
sarcoplasmic reticulum and release calcium into the
sarcoplasm. Some of this calcium attaches to troponin, causing a conformational change that moves tropomyosin out of the way so that the cross bridges can attach to actin and produce muscle contraction.
Troponin is found in both skeletal muscle and cardiac muscle, but the specific versions of troponin differ between types of muscle. The main difference is that the TnC subunit of troponin in skeletal muscle has four calcium ion binding sites, whereas in cardiac muscle there are only three.
Discussions of troponin often pertain to its functional characteristics and/or to its usefulness as a diagnostic marker for various heart disorders.
Functional characteristics
Role of troponins
Both cardiac and skeletal muscles are controlled by changes in the intracellular
calcium concentration. When calcium rises, the muscles contract, and when calcium falls the muscles relax.
Troponin is a component of thin filaments (along with actin and tropomyosin), and is the protein to which calcium binds to accomplish this regulation. Troponin has three subunits, TnC, TnI, and TnT. When calcium is bound to specific sites on TnC, tropomyosin rolls out of the way of the actin filament active sites, so that myosin (a molecular motor organized in muscle thick filaments) can attach to the thin filament and produce force and/or movement. In the absence of calcium, tropomyosin interferes with this action of myosin, and therefore muscles remain relaxed.
Troponin I has also been shown to inhibit angiogenesis in vivo and in vitro.
Individual subunits serve different functions:
- Troponin C binds to calcium ions to produce a conformational change in TnI
- Troponin T binds to tropomyosin, interlocking them to form a troponin-tropomyosin complex
- Troponin I binds to actin in thin myofilaments to hold the troponin-tropomyosin complex in place
Diagnostic use
Certain subtypes of
troponin (cardiac troponin I and T) are very sensitive and specific
indicators of damage to the
heart muscle (
myocardium). They are measured in the
blood to differentiate between unstable
angina and
myocardial infarction (heart attack) in patients with
chest pain. A patient who had suffered from a myocardial infarction would have an area of damaged heart muscle and so would have elevated cardiac troponin levels in the blood.
It is important to note that cardiac troponins are a marker of all heart muscle damage, not just myocardial infarction. Other conditions that directly or indirectly lead to heart muscle damage can also therefore increase troponin levels:
Detection of cardiac troponin
Cardiac troponin T and I are measured by immunoassay methods. Due to patent regulations a single manufacturer distributes cTnT. A host of diagnostic companies make cTnI immunoassay methods available on many different immunoassay platforms.
Detection of cardiotoxicity and cardioprotection
Drug-induced cardiotoxicity is common to all classes of therapeutic drugs. It is essential that cardiotoxicity is detected with a high degree of sensitivity and specificity. The newly developed troponins are especially useful in this context Similarly, cardioprotective effects of therapeutic intervention is paramount in preserving myocardial integrity, especially during general surgery. Sensitive assays for cardiac troponin can be used to monitor the protective effects of intervention.
Cardiac troponin I, in a community-based cohort study indicating the importance of silent cardiac damage, has been shown to predict first CHD event in men free from CVD at baseline, and death.
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