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Lecture 7 - Genome Tools

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Modifying proteins<br />

•Mimicking natural mutations<br />

•Protocols to change specific amino acids encoded by a cloned gene<br />

•Therapeutic and industrial applications<br />

•Desired results:<br />

•Alter Michaelis constant Km- reflects substrate binding strength<br />

•Maximal rate of conversion Vmax<br />

•[improves efficiency of enzyme-catalyzed reaction Vmax/Km]<br />

•Change thermal tolerance, pH stability<br />

•Modify active site and structure in nonaqueous solvents, non-physiological conditions<br />

•Alter need for co-factor or change co-factor<br />

•Modify substrate-binding site to increase specificity, decrease side reactions<br />

•Link enzymes/proteins together<br />

•Increase resistance to proteases, extending half-life<br />

•Alter allosteric regulation events<br />

•“Addressing” /”export” issues of the protein<br />

•Purification issues<br />

•“Tracking” or visualization of protein

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