Plasma Proteins & Immunoglobulins Flashcards
(41 cards)
B1-globulin glycoprotein
Transferrin
- 2 mols Fe per mol of Tf
- Tfr1 and Tfr2 - receptors that bind iron to facilitate endocytosis
A2-globulin plasma protein
Ceruloplasmin
1 mole of ceruloplasmin binds __ atoms of copper VERY TIGHTLY
6
Transmembrane protein in enterocyte with ferroxidase activity
Hephaestin
- Converts ferrous to ferric for transport across plasma membrane
Carries Fe across basolateral membrane
Ferroportin
Transfers iron from apical surface of enterocytes into their interiors
DMT1 (Divalent Metal Transporter)
Protein that stores iron (Fe3+, ferric) in enterocytes for future use
Ferritin
High Fe levels: Fe _______ to IRE-BP that ________ binding of IRE to mRNA, leading to synthesis of _______ and degradation of ________
High Fe levels: Fe BINDS TO to IRE-BP that PREVENTS binding of IRE to mRNA, leading to synthesis of FERRITIN (storage of iron) and degradation of TfR
Low Fe levels: Fe _______ to IRE-BP that ________ binding of IRE to mRNA, leading to synthesis of _______ and degradation of ________
Low Fe levels: Fe DOES NOT BIND to IRE-BP that ALLOWS binding of IRE to mRNA, leading to synthesis of TfR (Fe transport) and degradation of ferritin
Osmotic pressure % d/t albumin
80%
Major protein of human plasma
Albumin (60%)
- NOT glycosylated
Plasma glycoprotein that binds extracorposcular Hb
Haptoglobin (Hb-Hp complex)
Half life of Hp
5 days
Half-life of Hb-Hp complex
90 mins
Plasma protein not synthesized in the liver
Gamma-globulins (membrane-bound polyribosomes)
Iron in enterocytes of proximal duodenum is in the (A) form due to the action of (B) enzyme
(A) ferrous state (Fe2+)
(B) ferrireductase
Copper is carried by (A) to liver and leaves the liver through (B)
(A) albumin
(B) ceruloplasmin
Disorder with mutation in ATP7A gene
Menke’s disease
ATP7A gene - copper-binding P-type ATPase
X-linked d/o of copper metabolism
Menke’s disease
Kayser-Fleischer ring
Wilson’s disease
Mutation in ATP7B gene
Wilson’s disease
ATP7B protein - copper-binding P-type ATPase
Drug that chelates copper
Penicillamine
Genetic disease wherein copper can’t be excreted from bile and accumulates in the liver, brain, kidney, and RBC
Wilson’s disease
Copper toxicosis
Inhibits trypsin, elastase and certain protease
α1-antiproteinase