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immune system and response
Humoral immune response
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Created by
Nayana Mistry
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Cards (8)
B cells are activated when chemicals are released from
T
helper cells or the antibody molecules on their cell surface bind to a
complementary
antigen.
Once they are activated, the B cells divide by
mitosis
and
differentiate
into two kinds of cell - plasma cells and memory cells
A)
plasma
B)
memory
2
B-lycophytes are involved in the
humoral
response (made in the
bone
marrow) and produce
antibodies
B-cell activation:
B cells collide with complementary
Helper
T Cell receptors and activates the B Cell to go through
clonal
selection
B cells are activated and undergo
mitosis
to make a large number of cells that
differentiate
into
plasma
cells and
memory
cells
B plasma cells make
antibodies
B memory cells can
divide
rapidly into
plasma
cells when re-infected with same pathogen to make large number of
antibodies
antibodies are a
quaternary
structured
protein
made up of 4
polypeptide
chains held together by
disulphide
bridges
variable
region/ light chain where antigen
binding
site is located
complementary
to specific antigen
constant region/
heavy
chain which is the
same
for all antibodies
A)
disulphide bridges
1
How antibodies work:
Agglutination
= antibodies contain 2
binding
sites so bind to 2 antigens at a time so they are
clumped
together for phagocytes to
engulf
Neutralising
agent = some pathogens release
toxins
which make us ill but antibodies
neutralise
them
blocking access to
human
cells = when antibody bind to pathogen it prevents antigen fitting in
host
receptors so it cant get inside
antibodies are
proteins
that have binding sites
complementary
to antigens and
destroy
the pathogen
Antibiotics work by interfering with
bacterial
cell
walls
and
ribosomes
metabolic reactions, either killing the bacteria or stopping its growth
no effect on viruses or our own cells because:
Viruses do not have
ribosomes
or cell
walls
(they use
hosts
ones) = antibiotic treatment is ineffective against bacteria
Human
cells do not have cell
walls
and we do have ribosomes, but these are
bigger
than those found in bacteria and
unaffected
by antibiotics
What is the role of the disulfide bridge in forming the quaternary structure of an antibody?
Joins
two (different)
polypeptides
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