RecA - A Molecular Motor
August 31st, 2007 by
Mike Gene
As you can see, the RecA story has turned out to be quite interesting and there is plenty more to talk about. But since this blog is not called “The Land of RecA,” I think I’ll give this subject a rest for now. However, as a parting gift, I offer up this bit of research which highlights just what a sophisticated little device we have here:
Now, Julia Cox, Oleg Tsodikov, and Michael Cox present evidence indicating that filaments of the bacterial RecA protein, long known for their role in homologous recombination and DNA repair, have properties reminiscent of a molecular motor as well.
[…]
The authors note that there are approximately six RecA molecules per helical turn in a RecA filament. They propose that the RecA molecules hydrolyzing ATP at any given moment are aligned in a “stripe” that runs along the side of the filament. This stripe of ATP hydrolysis moves around the fiber in a repeating pattern of six steps. At the 5′ end of the fiber, ATP hydrolysis leads to RecA release. But in the middle of the fiber, it could work as a rotary motor, with the power to wind or unwind DNA and drive strand invasion through difficult passages of damaged DNA.
Sweet. Here’s a picture of the stripe along the RecA filament, making it easier to envision the coordinated ATP hydrolysis being converted into rotary motion within the tube that winds or unwinds the DNA.

And for those interested, here is the study: Organized Unidirectional Waves of ATP Hydrolysis within a RecA Filament
Posted in General |

September 12th, 2007 at 8:48 pm
[…] I mentioned before that RecA was a motor protein . Well, recent data confirm this. : Additional biophysical and biochemical analyses revealed that RecA family proteins may couple ATP binding and hydrolysis to the DNA strand exchange reaction in a manner that promotes clockwise axial rotation of nucleoprotein filaments. Specially, the 61 RadA helical filament undergoes clockwise axial rotation in 2 discrete 120° steps to the 31 extended right-handed filament and then to the 43 left-handed filament. As a result, all the DNA-binding motifs (denoted L1, L2 and HhH) in the RadA proteins move concurrently to mediate DNA binding, homology pairing, and strand exchange, respectively. Therefore, the energy of ATP is used to rotate not only DNA substrates but also the RecA family protein filaments. […]