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Immunoglobulins (Ig)
proteins produced by B lymphocytes as part of the humoral immune response to non-self molecules
Fab
the antigen-binding fragment of an immunoglobulin generated by Papain digestion
Fc
the crystal fragment of an immunoglobulin that cannot bind antigen but can bind and activate immune cells and complement
IgA
an immunoglobulin class found in the intestinal tract
IgD
an immunoglobulin class that acts as a cell-surface receptor on B lymphocytes
IgE
an immunoglobulin class found in minute quantities in serum that is involved in the response to parasites and in the allergic response
IgG
the major class of immunoglobulin in serum that can cross the placenta via receptor-mediated endocytosis
IgM
the first immunoglobulin class to be raised
Opsonisation
the process of labelling for phagocytosis utilizing the Fab and Fc regions
Epitope
an antigenic determinant that is represented by atoms in contact with the heavy and light chains
Nanobodies
single-domain
Myoglobin (Mb)
a protein that binds O2 in the muscle and acts like a store or sponge
Haemoglobin (Hb)
a tetramer protein that binds O2 and acts as a carrier in the blood
Haem
a prosthetic group consisting of Fe2+ in a protoporphyrin IX ring
Metmyoglobin
the Fe3+ form of myoglobin that cannot bind oxygen
p50
the pO2 level at which half of the myoglobin molecules are bound to O2
Deoxy Hb
the tense (T) form of haemoglobin that features low oxygen affinity
Oxy Hb
the relaxed (R) form of haemoglobin that features high oxygen affinity
Hill plot
a log/log graph used to display binding characteristics and cooperativity
2
3-Bisphosphoglycerate (2
Bohr shift
the phenomenon where increased H+ and CO2 concentrations reduce haemoglobin's oxygen affinity
Carboxyhaemoglobin
the all-R form of haemoglobin resulting from carbon monoxide binding
Methaemoglobinaemia
a condition causing blue skin resulting from an inherited deficiency of methaemoglobin reductase and the oxidation of haem to the Fe3+ form
Haemoglobin S (HbS)
an abnormal haemoglobin caused by a point mutation (Glu to Val) that distorts red blood cells and polymerizes to form long filaments in sickle cell anaemia
Thalassaemias
diseases characterized by a lack of one or the other subunit (alpha or beta) of haemoglobin
Haemoglobin F (HbF)
fetal haemoglobin which consists of two alpha and two gamma subunits