Final answer:
In Hb S, a valine residue binds to a hydrophobic patch causing aggregation of the hemoglobin, resulting in the sickle shape of red blood cells in sickle cell anemia.
Step-by-step explanation:
In Hb S, a valine residue binds to a(n) hydrophobic patch causing aggregation of the hemoglobin. In Hb S, a valine residue binds to a hydrophobic patch causing aggregation of the hemoglobin, resulting in the sickle shape of red blood cells in sickle cell anemia.
The hemoglobin molecule normally forms a colloidal suspension inside red blood cells, allowing them to easily deform and deliver oxygen. However, in sickle cell anemia, the substitution of a hydrophilic amino acid with a hydrophobic amino acid leads to the abnormal hemoglobin molecules aggregating and forming long fibers, causing the red blood cells to deform into a sickle shape.