Sandbox GGC11
Alpha- Crystallin AB Chain
Alpha Crystallin a hetero-oligameric complex with a size of about 700 to 800 kDa. [1] Alpha A and Alpha B Crystallin are proteins that encoded by the genes CRYAA and CRYAB. Alpha A and B are a major protein component of the mammalian eye lens that makes up about 40% of the eye lens protein. Alpha A crystallin is mainly found on the lens of the eye with trace amounts in other tissues while Alpha B is essentially considered a ubiquitous protein. [2] Alpha Crystallin is part of the small heat- shock protein family that has a conserved homologous sequence of 90 to 100 residues [3] FunctionThis protein contributes to the transparency and refractive index of the eye lens. Alpha- Crystallin can act as chaperones preventing the aggregation of various proteins. Even though they act as molecular chaperones, they don't renature proteins and release them like true chaperones do; instead, they hold proteins in large soluble aggregates. [4] It's chaperone properties gives the ability to prevent aggregation of denatured proteins and increase stress tolerance for cell. [5] Also, it has been shown that Alpha B chain is involved in the inhibition of apoptosis [6] DiseaseCataracts 9, multiple types This disease is caused by mutations affecting the eye lens. One of those mutations is usually R116C where an arginine is mutated to a cysteine. R116C is generally linked to one form of autosomal congenital cataracts. Congenital cataracts refers to the opacification of the eye lens that occurs at birth while infantile cataracts refers to the opacification of eye lens that developed during the first year. [7] An opacification of the crystalline lens of the eye occurs, in most instances, may lead to impairment or blindness. Opacities vary in morphology it might be static or progressive. [8] Myopathy, Miofibrillar A group of chronic neuromuscular disorder characterized by the disintegration of the sarcomere Z disc and myofibrils. Myopathy is characterized by weakness of proximal and distal limbs, weakness of neck, hypertrophy cardiomyopathy, and cataracts in a subset of patients. [9] Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin This is another form of myopathy myofibril, but it happens in infants. It is a chronic neuromuscular disorder characterized by disintegration of sarcomere Z disc and myofibrils. MFMFIH-CRYAB has onset on the first weeks of life after the neonatal period. Affected infants show rapid muscular rigidity of trunks and limbs which is associated with increasing respiratory difficulties resulting in death before the age of 3. [10] Dilated Cardiomyopathy DCM is known to be caused by mutations sarcomere proteins including alpha crystallin b and titin also known as connectin. It's a condition where the heart muscle is enlarged and weakened. DCM is characterized by the dilation of ventricles accompanied by systolic dysfunction which can result in heart failure and arrhythmias. Alpha crystallin b is associated with this disease because a missense mutation of R157H was found in familial DCM. [11] RelevanceAlpha Crystallin A 1-172 is found at nearly 2 folds higher in diabetic lenses than an aged matched control lens. In humans, the alpha A gene is found in chromosome 21 and encodes for 173 amino acid residues while the alpha B gene is found in chromosome 11 and encodes for 175 amino acids.[2] In mammalian lens, the molar ratio between alpha A and alpha B is a 3 to 1 ratio. [12] During aging, the eye lens undergo post translational modification that can affect the transparency of the lens. There is an increase in the high molecular weight fraction and water soluble to insoluble fraction. [2] Due to the function of alpha crystallin a and b, all of this changes can occur without affecting the transparency of the eye lens. Furthermore, an increased level of Alpha Crystallin B chain has been associated with various diseases such Alexander's disease, Alzheimer's, and Parkinson's. [13] Structural highlightsThis structure highlight shows where Arg 116 is located in the A chain. A mutation of this amino acid to cysteine will lead to cataracts. [2] The following structure shows where Arg 120 on B chain is located. The mutation of this amino acid in the B chain of crystalline gene decreased interaction with wild-type CRYAA and CRYAB. However, it increases interactions with CRBB2 and CRYGC leading to cytoplasmic aggregation. [14] Also, when Arg is mutated to Gly, it causes desmin- related myopathy, cardiomyopathy, and cataracts. Also, this mutation reduces chaperone protection activity and in some target proteins promoted aggregation. [2] This highlight shows the location of the Histidine amino acids involved in inter-subunit bridging of Zn2+ ions which enhances stability.[15] This is crucial as there is no protein turnover in the lens. This structure shows Lys 72. When this amino acid is acetylated, there might be an increase the chaperone activity for the protein. Chaperon activity is highly necessary because it plays a critical role in maintaining lens transparency. [16] This structure highlights Asp 109. A mutation of asp 109 to his is associated with restrictive cardiomyopathy and aggregation of CRYAB and DES gene. This mutation reduces the localization of Desmin and alpha crystallin b in the Z band and intercalated disc of the myocardium. [17]. Also, when asp 109 is mutated to his is associated with myofibrillar myopathy and polar cataracts. [18] The following structure shows Alpha Crystallin Structure with all the chains that make it up.
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