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DNA and ATP binding activities of the baculovirus DNA helicase P143
1Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128, USA.
Journal of Virology
|July 4, 2001
Abstract:
P143 is a DNA helicase that tightly binds both double-stranded and single-stranded DNA. DNA-protein complexes rapidly dissociated in the presence of ATP and Mg(2+). This finding suggests that ATP hydrolysis causes a conformational change in P143 which decreases affinity for DNA. This supports the model of an inchworm mechanism of DNA unwinding.
Insights
The P143 DNA helicase binds DNA tightly, but ATP and Mg(2+) cause it to release DNA. This suggests an inchworm mechanism for DNA unwinding by P143.
Area of Science:
- Molecular Biology
- Biochemistry
- Genetics
Background:
- P143 is a protein involved in DNA replication and repair.
- DNA helicases are essential enzymes that unwind DNA.
- Understanding DNA helicase mechanisms is crucial for comprehending DNA metabolism.
Purpose of the Study:
- To investigate the DNA binding properties of P143.
- To elucidate the role of ATP hydrolysis in P143's DNA binding.
- To determine the mechanism by which P143 unwinds DNA.
Main Methods:
- DNA binding assays were performed to assess P143's affinity for double-stranded and single-stranded DNA.
- The effect of ATP and Mg(2+) on DNA-protein complex stability was measured.
- Data were analyzed to support or refute proposed DNA unwinding models.
Main Results:
- P143 demonstrated strong binding to both double-stranded and single-stranded DNA.
- DNA-protein complexes involving P143 rapidly dissociated in the presence of ATP and Mg(2+).
- These results indicate that ATP hydrolysis induces a conformational change in P143, reducing its DNA affinity.
Conclusions:
- ATP hydrolysis is critical for P143's DNA release.
- The findings support an inchworm model for P143-mediated DNA unwinding.
- P143 functions as a DNA helicase utilizing an ATP-dependent mechanism for DNA translocation.