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34 Cards in this Set

  • Front
  • Back
the complement system is the major effector of the....
humoral branch of the immune system
RBC + serum>
RBC + Ab>
RBC + serum + Ab>
ok
ok
lysed
is complement a single protein?
no it is 12 proteins
does complement affect innate or adaptive?
both
4 functions of complement

p
-lysis
-opsonization
-activatione of inflammatory response
-clearance of immune complexes

see page 169
complement makes up what fraction of serum globulin?
5%
what is complement designated by?
numerals (C1-C9)
letter symbols (factor D)
trivial names (homologous restriction factor)
talk about the a and b fragment
the b fragment is always larger....except in the case of C2
ccomplexes with enzymatic activity are designated by what over the symbol?
a bar will be over the symbol
3 basic pathways complement can be activated in....don't describe
-classical
-alternative
-lectin
Descibe the classical pathway

p. 170 and 172
170-172
how are C1-4 found in the plasma normally?
they are present in the plasma in functionally inactive forms
C1 structure, and interaction, and random tidbits

p. 170-171
C1qr2s2....it is a macromolecule with a molecule of q, 2 molecules of r and 2 molecules of s

-Structure is stabilized by calcium ion

-Each c1r and c1s monomer contains a catalytic domain with enzymatic activity and an interaction domain that facilitates binding with C1q or with each other
IgM bound to membrane antigen vs serum antigen and binding to C1
-membrane antigen will cause IgM to have stable conformation and will have 3 binding sites for C1

-circulating IgM, however, will be planar and there will be no C1q binding site
IgG activating classical complement pathway
It only has 1 binding site (remember IgM has 3)...and because of this, 2 molecules must be 30-40nm apart from each other on a target surface or in a complex

-a single molecule of igM bound to a rbc can activate complement system, but 1000 or more IgG molecules are needed to ensure that 2 molecules are close enough for to initiate c1q binding.
how does C4b2a bind to bind?
adjacent to antibody
anaphylatoxins for chemotaxis
Inflammation!
C3a- C5a
opsonization for uptake by
phagocytic cells
C3b, iC3b
Membrane attack complex (M.A.C.)
C5b-C9
biological consequences of complement activation
-opsonization for uptake by phagocytic cells

-anaphylatoxins for chemotaxis inflammation

-Membrane attack complex (MAC)
whats type of complement to phagocytic cells have receptors for?
C3
alternative pathway involves what four serum proteins?
c3, factor b, factor d and properdin
in most cases how is the alternative pathway initiated?
by cell surface constituents that are foreign to the host
what are some initiaters of alternative pathway complement activation?

p. 173
page 173

.....don't need to know all
talk about c3 in alternative pathway
c3 in serum has an unstable thioester bond: subject to slow spontaneous hydrolysis to yield C3a and C3b....c3b component can bind to foreign surface antigens....bacterial cells or viral particles
diagram the alternative pathway

p. 174
p. 174
what do the membranes of most mammalian cells have?
sialic acid: contributes to the rapid inactivation of bound C3b molecules on host cells: foreign cells do not have as much
what does serum c3 contain?
unstable thioester bonds....this leads it to spontaneous hydrolysis
what does the MAC eventually do?
forms a large channel through the membrane of the target cell, enabling ions and small molecules to diffuse freely across the membrane
what is the end result of the classical, alternative or lectin pathway?
production of an active C5 convertase
when does the complement cascade go from being on the hydrophillic surface of membranes or immune complexes to creating exposure for hydrophobic regions that will bind to membrane phospholipids?
as c5b6 binds to C7.....the hydrophobic binding sites allow it to anchor to the cell
what is the amplification step in all pathways
when c3 convertase converts c3 into c3a and c3b
talk about the MAC
-C5b6789

-initial C5b678 creates a 10A diameter pore....can lead to lysis of RBC's but not of nucleated cells

-final step is formation of the MAC is the binding and polymerization of C9, a perforin-like molecule, to the C5b678 complex...now has pore of 70-100A

p.178
wht are regulatory mechanisms necessary for complement
because elements of complement are capable of attacking host cells as well as foreign cells and microorganisms