This is a default text for your page Raia Hasan/Sandbox 1. Click above on edit this page to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia [1] or to the article describing Jmol [2] to the rescue.
Function
Clostridium botulinum is a rod-shaped, spore-forming bacteria that is highly pathogenic. These bacteria are prevalent in soils, sediments, and aquatic environments. The botulinum toxins decrease or prevent nerve function which leads to respiratory and muscular paralysis.
The spores within the C. botulinum grow an abundance of active bacteria and transform into neurotoxins to produce Botulinum Neurotoxin or Botulinum Toxin- one of the most toxic proteins known to exist.
There are four types of botulism that are associated with the bacteria, Clostridium botulinum.
These include food, wound, infant botulism, and inhalation botulism.
Types of Botulinum Neurotoxins
Botulinum Neurotoxins A is the first type of toxin to be introduced into the cosmetic world with the abbreviated name, Botox. Botox is mainly used for treating facial imperfections, muscle spasms, and other conditions like chronic migraines, dystonia, blepharospasms, diabetic neuropathy, spinal cord injury, epicondylitis incontinence, hyperhidrosis, and many more.
The mechanism of action for type A: Consists of a heavy chain (100 kDa) and light chain (50 kDa) which are linked together by a single disulfide bond. It is a 150- kDa molecular weight protein that inhibits the release of acetylcholine by blocking the neuromuscular communications and transmissions on motor and sympathetic nerve terminals. The heavy chain binds at the pre-synaptic surface of cholinergic neurons. They bind one way and are irreversible. Endocytosis allows for the toxin receptor- complex to be sent into the cell after binding. The botulism toxin enters the cytoplasm after the disulfide bond between the two chains is broken. The light chain interacts with SNAP-25 (needed for binding/ attachment and release of ACH from vesicles) specifically at the nerve terminal to prevent binding of acetylcholine vesicles with the cell membrane. ^6
is produced through the process of fermentation to block acetylcholine release for the treatment of dystonia and sialorrhea.
Mechanism of Action for Type B: Binds and cleaves VAMP- which is part of the protein complex that is known for docking and fusion of the presynaptic membrane to the synaptic vesicles.
Botulinum Neurotoxin type C: generates apoptotic cell death in cerebellar (area in the brain that is responsible for coordination and balance) neurons acting in birds mostly but can also be seen in some mammals and fish
Botulinum Neurotoxin type D: causes a periodic onset of the fatal disease, botulism. This occurs mostly in horses and cattle and is rarely found in humans 88. Its mechanism of action is by inhibiting the discharge of TNF from monocytes.
Botulinum neurotoxin type D/C: attaches and efficiently enters into the neurons that don’t have complex gangliosides. Complex glycosphingolipids are acidic glycosphingolipids that have sialic acid groups. Type D/C recognizes the sialic acid only but no other gangliosides' moieties.
Disease
How Botox is being used to treat migraines? A migraine is a severe headache that results in throbbing pain or a pulsing sensation on one side of the head. It can last from hours to days and is followed by multiple symptoms such as nausea, vomiting, and sensitivity to light and sound. In recent studies, it was found that Botulinum neurotoxins A or Botox is being used to stop the migraines signals and leading factors to stop a migraine from occurring at all. A medical professional uses Botox to inject into seven specific areas around the head and surrounding the neck. Those areas include the forehead, bridge of the nose, the temples, the neck, the back of the head, and above the shoulder blades in the upper back, leading to around thirty-one injections within each treatment. Typically a person with a migraine would get nearly 4 treatments per year.
How Botox is being used to treat Cervical dystonia? This disease is also known by the name Spasmodic Torticollis in which the neck muscles involuntarily contract. The neck contraction causes the head to twist and move to the side, and tilt forward or backward uncontrollably. Jerking movement could be chin toward the shoulder, ear toward the shoulder, chin straight up, chin straight down. Botox can be a temporary treatment by preventing the nerve signals that cause the spontaneous muscle spasms from getting to the dystonic muscles thus putting a stop to the involuntary spasms.
How Botox is being used to treat Sialorrhea? Sialorrhea is producing excessive saliva or drooling involuntarily. This problem is mostly found in neurologically affected children such as cerebral palsy patients and in adults who have been diagnosed with Parkinson's disease. In some cases, excessive salivation may be present in patients who have had a stroke. This is most commonly caused by an inability to have full control of the oral and facial muscles. Botox is injected into the salivary glands to temporarily decrease saliva output.
How is Botox used in the cosmetic world? A greater majority of the time, Botox is inserted into the skin via a syringe. Cosmetic procedures are the most common use of Botox applications. Once the liquid botox is inserted into the skin, the muscle contracts and is unable to move. Botox can be used for facial wrinkles, frown lines, forehead lines, top of the nose (bunny lines), etc. to improve or enhance facial features.
Structural highlights
Consists of a which are linked together by a single disulfide bond. It is a 150- kDa molecular weight protein that inhibits the release of acetylcholine by blocking the neuromuscular communications and transmissions on motor and sympathetic nerve terminals. The heavy chain binds at the pre-synaptic surface of cholinergic neurons. They bind one way and are irreversible. Endocytosis allows for the toxin receptor- complex to be sent into the cell after binding. The botulism toxin enters the cytoplasm after the disulfide bond between the two chains is broken. The light chain interacts with SNAP-25 (needed for binding/ attachment and release of ACH from vesicles) specifically at the nerve terminal to prevent binding of acetylcholine vesicles with the cell membrane.
"Botulinum toxin is a that acts on vulnerable cells to cleave polypeptides that are essential for exocytosis"(Simpson)
