Myoglobin is a cytoplasmic hemoprotein composed by a single polypeptide chain of 154 amino acids. It is expressed
solely in cardiac myocytes and oxidative skeletal muscle fibers. Myoglobin was so named because of its functional and structural
similarity to hemoglobin. Like hemoglobin, myoglobin binds reversibly to O2 and thus may
facilitate the transport of O2 from red blood cells to the mitochondria
during periods of increased metabolic activity or serve as an O 2
reservoir during hypoxia or anoxia.The
structure of myoglobin was first delineated by John Kendrew more than
40 years ago and subsequent work has shown that it is a polypeptide
chain consisting of eight α-helices. It binds oxygen to its heme residue, a porphyrin ring with an iron ion. The
polypeptide chain is folded and packs the heme prosthetic group,
positioning it between two histidine, His64 and His93 residues. The
iron ion interacts with six ligands, four of which are supplied by the
nitrogen atoms of the four pyrrhols and share a common plane. The
side chain imidazole of His93, provides the fifth ligand, stabilizing
the heme group and slightly displacing the iron ion out of the heme
plane. The
position of the sixth ligand, in deoximoglobin, serves as the
binding site for O2, as well as for other potential ligands, such as CO
or NO. When O2 binds, the iron ion, it is partially drawn back toward the porphyrin plane. Although
this shift is of little importance in the function of monomeric
myoglobin, it provides the basis for the conformational changes that
underlie the allosteric properties of tetrameric hemoglobin. In addition, studies using X-ray diffraction and xenon binding
techniques have identified four highly conserved internal cavities
within the myoglobin molecule that can help target molecules to bind to the heme residue.Related to its role as an O2 reservoir, myoglobin also functions as an intracellular pO2 buffer (partial pressure of O2). Similarly
to the role of creatine phosphokinase, which works to buffer ATP
concentrations when muscle activity increases, myoglobin works to buffer
O2 concentrations. As
a result, the intracellular concentration of O2 remains relatively
constant and homogeneous, despite increases in O2 flow from the
capillaries to the mitochondria, induced by physical activity.
Text written by:
Ana Rita Cardoso
João Faria
Joel Mateus
Pedro Desport .