As mentioned in the introduction to this chapter, we now know that repressor acts by binding to the operator and preventing RNA polymerase from binding to the lac promoter. The first experiments to show that repressor binds to lac DNA used ultracentrifugation of radioactive repressor and the DNA from λlac phage. The DNA sediments at 40S, whereas repressor sediments at 7S. If repressor bound so tightly to DNA that it did not come off during the centrifugation, it would sediment at about 40S. Indeed, DNA containing lac carried lac repressor along with it down the centrifuge tube, but only if inducers of the lac operon were not present (Fig. 1). These are the properties expected of repressor if it were to regulate by binding to DNA to prevent transcription.

Fig1. Repressor binds to operator-containing DNA only in the absence of IPTG.

A considerably easier assay of DNA binding by lac repressor was developed later by Riggs and Bourgeois. Pure lambda DNA passes through cellulose nitrate filters, but repressor, like many other proteins, binds to the filters. It is bound by molecular interactions and not by filtration. Most surprisingly, if repressor is bound to DNA, the DNA molecule will not pass through the filter either. Thus if the DNA is made radioactive, the retention of lac DNA on the filter can easily be detected, providing a simple assay for repressor binding to operator (Fig. 2).

Fig2. Schematic of the filter binding assay for lac repressor.

The filter-binding assay is very sensitive because the DNA can be made highly radioactive with ³²PO4 The long DNA molecule contains many phosphate groups, and the half-life of ³²P is short. This assay facilitated measurement of the rates of binding and dissociation as well as a determination of the equilibrium constant for binding.

For example, the rate of lac repressor dissociation from operator is easily measured by mixing repressor with radioactive DNA so that the majority of repressor is bound to operator. Then the solution is diluted and a large excess of nonradioactive lac DNA is added. Any repressor that subsequently dissociates from operator either remains free in solution or has a much greater chance of binding to nonradioactive DNA. At intervals after the dilution, the mixture is filtered to determine the fraction of repressor still bound to the radioactive lac operator-containing DNA. The kinetics in the reduction in the amount of radioactive DNA bound to the filters with increasing time give the dissociation rate of repressor from operator.

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مواضيع ذات صلة

Targeting of Mitochondrial Proteins

Intra-Golgi Transport and Protein Processing

Cotranslational Protein Translocation Into the Endoplasmic Reticulum

The Isolation and Structure of Operator

The Migration Retardation Assay and DNA Looping

Detection and Purification of lac Repressor

The Difficulty of Detecting Wild-Type lac Repressor

An Assay for lac Repressor

Proving lac Repressor is a Protein

The Role of Inducer Analogs in the Study of the lac Operon

Background of the lac Operon

Mutagenesis with Chemically Synthesized DNA