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Biophysical studies of membrane proteins/peptides. Interaction with ...

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PROTEIN-PROTEIN AND PROTEIN-LIPID INTERACTIONS<br />

OF M13 MCP<br />

II<br />

1. Introduction<br />

PROTEIN-PROTEIN AND<br />

PROTEIN-LIPID<br />

INTERACTIONS OF M13<br />

MAJOR COAT PROTEIN<br />

The M(unich)13 bacteriophage was discovered in 1963 by P. H. H<strong>of</strong>schneider in an<br />

incubation <strong>of</strong> waste water samples <strong>with</strong> Escherichia coli bacteria. It belongs to the large<br />

family <strong>of</strong> filamentous phages (Inoviridae), which comprise some <strong>of</strong> the smallest<br />

bacteriophages known (Spruijt et al., 1999).<br />

These viruses are able to infect bacteria <strong>with</strong>out great disturbance <strong>of</strong> the host cells.<br />

In this way, reproduction <strong>of</strong> the virus inside the host goes on as cells continue to grow<br />

and divide even if at a reduced rate. For efficient infection, filamentous phages require<br />

expression <strong>of</strong> pili on the surface <strong>of</strong> the host bacteria. The pili acts as a receptor site, and<br />

depending on the specificity for pili interaction, filamentous bacteriophages are divided<br />

in different classes. The M13 bacteriophage belongs to the Ff group, which is only able<br />

to infect E. coli cells carrying sex pili (Spruijt et al., 1999). Genetic manipulation <strong>of</strong><br />

plasmids derived from the M13 bacteriophage proved to be relatively easy, and this<br />

allowed the M13 genome to be widely used as a cloning vector (Spruijt et al., 1999).<br />

One <strong>of</strong> the factors that contributed to the enormous popularity <strong>of</strong> the M13<br />

bacteriophage in biotechnology was its relatively simple architecture. The phage<br />

47

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