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i- Review ofLiterature 5. High density lipoproteins: are oftwo main types, HDL2 and HDL3. They probably transported from peripheral cells to the liver, prior to excrerion (Beckett, 1998). The apolipoproteins: The protein components ofthe lipoproteins, the apolipoproteins are a complex family of polypeptides that promote and control the lipid transport in plasma and uptake into tissues. They are classified into five main groups (ape-A, B, C, E and (a)), some ofwhich may be subdivided, and lastly apo (a). Apo A: these are synthesized in the liver and intestine. They are initially present in chylomicrons in lymph, but they rapidly transfer to lIDL. Apo B: is present in plasma in two forms, apoB100 and apoB48 chyle micron. ApaB100 is the protein component of LDL and is also present in VLDL and LDL . ApoB100 is recognized by specific receptors in peripheral tissues. Apo C: is a family of three proteins (apo CI, apo ClI and apo ClII) is synthesized in the liver and incorporated into HDL and LDL, chylomicron. Apo E: is synthesized in the liver, incorporated into HDL and transferred in the circulation to chylomicrons and VLDL. There are three major isoforrns (apoE2, apoE3 and apoE4) at a single genetic locus giving rise to genotypes (E3/3, E2/3, E2/4, etc.). Apo E is probably mainly involved in the hepatic intake of chylomicron remnants and IDL, tissues (Walker, 1990). since it binds to apo B receptors in-the Lipoprotein (a) "LP (a)": The lipoprotein (a) is sixth type oflipoprotein particles. It was first deteced in 1962. It consists of LDL particle to which a long polypeptide chain is attached by a disulfide bridge a single apo (a) having a high 61
Review ofLiterature carbohydrate content and having a similar amino acid sequence to plasminogen, and is attached by a disulfide bond to the apoBl00. It is synthesized in the liver with a poor clearance from plasma it has 11 phenotypes and 19 genotypes (Howard and pizzo, 1993). Lp (a) is carried in plasma on a protein carrier apolipoprotein (a) which was found to have a 90% structural homology to plasminogen. Inheritance of apolipoprotein (a) is controlled by a specific gene on chromosome No.6 (Wang et al., 1994). Lipoprotein(a) LP(a) is a distinct class oflipoprotein (as shown in table 3) that is structurally related to LDL, because both lipoprotein classes possess one molecule ofapo B-100 per particle and have similar lipid compositions.(Durington,1995 & Marcovina, ,1995) However unlike LDL, Lp(a) contains a carbohydrate-rich protein apo(a) that is covalently bound to the apo B-lOO through a disulfide linkage. The available evidence suggest that Lp(a) contains one molecule ofapo(a) and one molecule of apo B-IOO per Lp(a) particle (Albers, et al. 1996). Apo(a) is the unique protein componant of Lp(a) and exhibits a significant sequence homology with plasminogen and a high degree of variation in polypeptide chain length. Apo(a) is composed ofa serine protease domain and a kringle-containing domain unlike plasminogen, however, Lp(a) is not activated to form an active protease. The kringle that is contiguous with the protease domain, kringle 5, shares 85% amino acid homology with plasminogen kringle 5, whereas the kringle 4 domain has 78 to 88% amino acid homology with kringle 4 ofplasminogen. Apo(a) contains 10 distinct classes ofkringle 4-1ike domains that differ from each other in amino acid sequence. Kringle 4 type I and kringle 4 types3 to 10 are present as a single copy on apo(a) particles. In contrast, kringle 4 type 2 is present in variable number ofrepeats (3 to> 40) and 62
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i-<br />
Review ofLiterature<br />
5. High density lipoproteins: are oftwo main types, HDL2 and HDL3.<br />
They probably transported from peripheral cells to the liver, prior to<br />
excrerion (Beckett, 1998).<br />
The apolipoproteins:<br />
The protein components ofthe lipoproteins, the apolipoproteins are<br />
a complex family of polypeptides that promote and control the lipid<br />
transport in plasma and uptake into tissues. They are classified into five<br />
main groups (ape-A, B, C, E and (a)), some ofwhich may be subdivided,<br />
and lastly apo (a).<br />
Apo A: these are synthesized in the liver and intestine. They are initially<br />
present in chylomicrons in lymph, but they rapidly transfer to lIDL.<br />
Apo B: is present in plasma in two forms, apoB100 and apoB48 chyle<br />
micron. ApaB100 is the protein component of LDL and is also present in<br />
VLDL and LDL . ApoB100 is recognized by specific receptors in<br />
peripheral tissues.<br />
Apo C: is a family of three proteins (apo CI, apo ClI and apo ClII) is<br />
synthesized in the liver and incorporated into HDL and LDL,<br />
chylomicron.<br />
Apo E: is synthesized in the liver, incorporated into HDL and transferred<br />
in the circulation to chylomicrons and VLDL. There are three major<br />
isoforrns (apoE2, apoE3 and apoE4) at a single genetic locus giving rise<br />
to genotypes (E3/3, E2/3, E2/4, etc.).<br />
Apo E is probably mainly involved in the hepatic intake of<br />
chylomicron remnants and IDL,<br />
tissues (Walker, 1990).<br />
since it binds to apo B receptors in-the<br />
Lipoprotein (a) "LP (a)":<br />
The lipoprotein (a) is sixth type oflipoprotein particles. It was first<br />
deteced in 1962. It consists of LDL particle to which a long polypeptide<br />
chain is attached by a disulfide bridge a single apo (a) having a high<br />
61