Receptor for bacteria

CFTR has a single-channel conductance of about 8 pS. It is present in the apical membranes of many epithelia. Its mutation leads to the potentially lethal disease cystic fibrosis. In addition to acting as a chloride channel, CFTR is also thought to regulate, e.g., the epithelial sodium channel ENaC, a molecularly unknown outwardly-rectifying chloride channel, and possibly also potassium channels and water channels. Some of these potential regulatory processes, however, are controversial. CFTR also acts as a receptor for bacteria. 

N. Sharon Oligomannoside units of membrane glycoproteins as receptors for bacteria... 

At the interface between the oral environment and the enamel surface, the salivary pellicle also exerts selectivity for bacterial adherence and is involved in the early stages of microbial biofilm formation (see below). Components of the pellicle serve as receptors for bacteria. Modification of the pellicle by host and bacterial enzymes may alter the functional characteristics of the pellicle surface, thereby influencing attachment of bacteria. 

Lingwood, C. A., Oligosaccharide receptors for bacteria a view to a kill, Curr Biol, 1998, 2 695-700. 

GANGLIOSIDES AS RECEPTORS FOR BACTERIA, VIRUSES, AND BACTERIAL TOXINS... 

In general, virus receptors carry out normal functions in the cell. For example, in bacteria some phage receptors are pili or flagella, others are cell-envelope components, and others are transport binding proteins. The receptor for influenza vims is a glycoprotein found on red blood cells and on cells of the mucous membrane of susceptible animals, whereas the receptor site of poliovirus is a lipoprotein. However, many animal and plant viruses do not have specific attachment sites at all and the vims enters passively as a result of phagocytosis or some other endocytotic process. 

The Fur protein regulates iron uptake systems in many Gram-negative bacteria. The striking phenotype of the first fur mutants isolated was the overexpression of the outer membrane receptors for siderophore iron transport. In addition, excretion of siderophores under iron-rich growth conditions was observed in these mutants, indicating that the biosynthesis of siderophores is also regulated by Fur. 

Specific receptors for siderophores and vitamin B12 have been identified in the OM of Gram-negative bacteria. The translocation of these ligands across the outer membrane follows an energy-dependent mechanism and also involves the TonB, ExbB, ExbD proteins anchored in the cytoplasmic membrane. Biochemical and genetic data indicate that these proteins form a functional unit (the Ton complex), which couples the outer membrane receptor-mediated... 

Figure 1.4. Recognition of bacteria by neutrophils. Invading bacteria are opsonised by serum proteins, such as complement fragments (e.g. C3b) and immunoglobulins. The plasma membranes of neutrophils possess receptors for these opsonins (e.g. Fc receptors and complement receptors). Thus, occupancy of these opsonin receptors triggers phagocytosis and activates events such as the respiratory burst and degranulation. Note that the receptors and opsonins are not drawn to scale.

Figure 18.4 Effects of cytokines on fate of iron during an infection. Transferrin is the form in which iron is transported in the blood (Chapter 15). Cytokines increase the number of ferritin receptors in proliferating lymphocytes, to facilitate the uptake of iron by lymphocytes. They also stimulate synthesis of apofer-ritin in the liver, which removes iron from the blood to reduce that available for bacteria. (See Chapter 15 for discussion of iron metabolism)...

Occupied receptors for adrenaline, glucagon, ACTH, and histamine activate adenylate cyclase via Gs proteins. Other Gs proteins, which contain subunits designated aolf and which exist as a number of subtypes, mediate olfactory responses. Subunit aD is another specialized polypeptide which is located primarily in neural tissues. A variety of additional G proteins have been discovered in organisms ranging from bacteria to mammals.179 183-186 All have similar structures with 39- to 45-kDa a subunits, 35- to 36-kDa (3 subunits and 5- to 8-kDa y subunits. Whereas the a subunits are unique to each G protein, (3 and y subunits may be shared among several G proteins. These proteins appear to function with many kinds of hormone receptors and... 

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