TY - JOUR
T1 - Structural Biology of Bacterial Haemophores
AU - Ascenzi, Paolo
AU - di Masi, Alessandra
AU - Leboffe, Loris
AU - Frangipani, Emanuela
AU - Nardini, Marco
AU - Verde, Cinzia
AU - Visca, Paolo
PY - 2015
Y1 - 2015
N2 - Iron plays a key role in a wide range of metabolic and signalling functions representing an essential nutrient for almost all forms of life. However, the ferric form is hardly soluble, whereas the ferrous form is highly toxic. Thus, in biological fluids, most of the iron is sequestered in iron- or haem-binding proteins and the level of free iron is low, making haem and iron acquisition a challenge for pathogenic bacteria during infections. Although toxic to the host, free haem is a major and readily available source of iron for several pathogenic microorganisms. Both Gram-positive and Gram-negative bacteria have developed several strategies to acquire free haem-Fe and protein-bound haem-Fe. Haemophores are a class of secreted and cell surface-exposed proteins promoting free-haem uptake, haem extraction from host haem proteins, and haem presentation to specific outer-membrane receptors that internalize the metal-porphyrins. Here, structural biology of bacterial haemophores is reviewed focusing on haem acquisition, haem internalization, and haem-degrading systems.
AB - Iron plays a key role in a wide range of metabolic and signalling functions representing an essential nutrient for almost all forms of life. However, the ferric form is hardly soluble, whereas the ferrous form is highly toxic. Thus, in biological fluids, most of the iron is sequestered in iron- or haem-binding proteins and the level of free iron is low, making haem and iron acquisition a challenge for pathogenic bacteria during infections. Although toxic to the host, free haem is a major and readily available source of iron for several pathogenic microorganisms. Both Gram-positive and Gram-negative bacteria have developed several strategies to acquire free haem-Fe and protein-bound haem-Fe. Haemophores are a class of secreted and cell surface-exposed proteins promoting free-haem uptake, haem extraction from host haem proteins, and haem presentation to specific outer-membrane receptors that internalize the metal-porphyrins. Here, structural biology of bacterial haemophores is reviewed focusing on haem acquisition, haem internalization, and haem-degrading systems.
KW - Bacterial haemophores
KW - Haem acquisition
KW - Haem degradation
KW - Haem internalization
KW - Structure–function relationships
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U2 - 10.1016/bs.ampbs.2015.09.002
DO - 10.1016/bs.ampbs.2015.09.002
M3 - Article
C2 - 26616517
VL - 67
SP - 127
EP - 176
JO - Advances in Microbial Physiology
JF - Advances in Microbial Physiology
SN - 0065-2911
ER -