We used the AFM as the primary imaging tool and have seen the complex form very clearly. We used both 100bp and 350bp long DNA in forming the complexes and they clearly form independently of the DNA length. It is interesting that the primary product in these constructs is that two DNA molecules bind to a protein tetramer and these complexes go on to aggregate by (non-specific?) binding of the protein oligomers, forming spider-like structures. We are in the process of examining the effect of EDTA on this secondary aggregation and to try even shorter DNA to form complexes. These should be easier to analyze.

Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2007
Total Cost
$14,945
Indirect Cost
Name
National Institute of Biomedical Imaging and Bioengineering
Department
Type
DUNS #
City
State
Country
United States
Zip Code