DR AMINA TARIQ BIOCHEMISTRY

DR AMINA TARIQ
BIOCHEMISTRY
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The ABO blood group system is the most
important blood type system (or blood group
system) in human blood transfusion.
The ABO blood group system wasdiscovered
by the Austrian scientist Karl Landsteiner,
who found three different blood types in
1900,he was awarded the Nobel Prize in
Physiology or Medicine in 1930 for his work.
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Blood has two main components: serum and
cells. Karl Landsteiner, a physician at the
University of Vienna, Austria, noted that the
sera of some individuals caused the red cells
of others to agglutinate.
Two years later, two of his students
discovered the fourth and rarest type, namely
AB.
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ABO substances are oligosaccharides present
in most cells of the body and in certain
secretions.
On membranes of red cells the
oligosaccharides that determine the specific
nature of ABO substances are present in
glycosphingolipids.
In secretions the oligosaccharides are present
in glycoproteins.
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Alleles at a locus independent of the ABO
blood group locus, known as the secretor
locus, determine an individual's ability to
secrete the ABO blood group substances in
saliva and other body fluids.
There are two genes, Se and se, where Se is
dominant to se. In other words, an individual
with at least one Se gene is a secretor.
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The antigens expressed on the red blood cell
determine an individual's blood group. The
main two blood groups are called ABO (with
blood types A, B, AB, and O) and Rh (with Rh
D-positive or Rh D-negative blood types).
Blood type O is the most common worldwide,
followed by group A. Group B is less
common, and group AB is the least common.
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People with blood type O are said to be
"universal donors" because their blood is
compatible with all ABO blood types.
Blood type AB individuals are known as
"universal receivers" because they can receive
blood from any ABO type.
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The H antigen is precursor to the ABO blood
group antigens. The H locus is located on
chromosome 19.
All humans contain enzymes which catalyze
the synthesis of the O antigen.
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The ABO blood group substances are
glycoproteins, the basic molecule of which is
known as the H substance. This H substance
is present in unmodified form in individuals
with blood type O. Adding extra sugar
molecules to the H substance produces the A
and B substances.
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H- substance itself is formed by the action of
a fucosyltransferase.
It catalyzes the transfer of fucose onto the
terminal galactose residue in α1-2 linkage.
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Humans with A-type blood also contain an
additional enzyme which adds NAcetylgalactosamine to the O antigen.
Humans with B-type blood contain another
enzyme which adds Galactose to the O
antigen.
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H(or O)
GalNAc transferase
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A substance
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H(or O)
Gal transferase
B substance
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Humans with AB-type blood contain both Atype and B-type enzymes.
While humans with O-type blood lack both
types of enzymes.
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An antigen is a substance, usually a protein
or a glycoprotein, which, when injected into a
human (or other organism) that does not
have the antigen, will cause an antibody to be
produced..
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Antibodies are a specific type of immunesystem proteins known as immunoglobulins,
whose role is to fight infections by binding
themselves to antigens.
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In the case of the ABO blood groups, the
antigens are present on the surface of the red
blood cell, while the antibodies are in the
serum.
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Individuals with type A blood can receive
blood from donors of type A and type O
blood.
Individuals with type B blood can receive
blood from donors of type B and type O
blood.
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Individuals with type AB blood can receive
blood from donors of type A, type B, type AB,
or type O blood.
Individuals with type O blood can receive
blood from donors of only type O.
Individuals of type A, B, AB and O blood can
receive blood from donors of type O blood.
Type O blood is called the universal donor.
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The second most important blood group in
humans is the Rhesus (Rh) system.
Landsteiner and Wiener discovered the Rh
blood group in 1940. They found that when
they injected rabbits with Rhesus monkey
blood; the rabbits produced antibodies
against the Rhesus red cells.
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The Rh blood group system is the major
cause of hemolytic anemia in the newborn.
A fetus who is Rh+ and whose mother is Rh−
is at high risk for this disorder, because the
mother will produce antibodies against the
fetal antigen.
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Anti-Rh+ antibody is injected into the mother
soon after her first delivery. This antibody
coats the fetal Rh+ cells in the mother's
circulation, which prevents them from
causing antibody production in the mother
and, therefore, her next child will not be at
risk for hemolytic anemia.
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Harpers Biochemistry
Teachers Notes