Ku protein

Structure of the Ku heterodimer bound to DNA

spinqualitylabelsall models Structure of the Ku heterodimer bound to DNA (PDB entry 1JEY) Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D PubMed Abstract The Ku heterodimer (Ku70 and Ku80 subunits) contributes to genomic integrity through its ability to bind DNA double-strand breaks and facilitate repair by the non-homologous end-joining pathway. The crystal structure of the human Ku heterodimer was determined both alone and bound to a 55-nucleotide DNA element at 2.7 and 2.5 A resolution, respectively. Ku70 and Ku80 share a common topology and form a dyad-symmetrical molecule with a preformed ring that encircles duplex DNA. The binding site can cradle two full turns of DNA while encircling only the central 3-4 base pairs (bp). Ku makes no contacts with DNA bases and few with the sugar-phosphate backbone, but it fits sterically to major and minor groove contours so as to position the DNA helix in a defined path through the protein ring. These features seem well designed to structurally support broken DNA ends and to bring the DNA helix into phase across the junction during end processing and ligation. Ku Ring Ku Ring The Ku Ring is composed of a broad base of beta barrels that cradle the DNA, and a narrow bridge that serves to protect the double strand break from base pairing with other DNA base pairs and degradation. There is little interaction between the ring and the backbone or base pairs of DNA; instead, the ring associates with DNA by the cradle fitting into the major grooves of the helix. The positive electrostatic charge caused by polarization of the ring also allows the negatively charged backbone of DNA to be guided into the correct position. The Ku protein also has a high affinity to DNA due to its form being preset for the helix. As a result of the asymmetric ring, there is a strong preference (Kd value of 1.5 to 4 X 10^-10 M) for the Ku Ring to slide onto the ends of DNA. In addition, other asymmetric features prevent the Ku protein from sliding further on the DNA helix. While wrapping over the entire helix, the Ku Ring is thin over the bridge, allowing ligases and polymerases to efficiently interact in non-homologous end joining (NHEJ). Domains Ku70/80 subunits Consisting of three domains (α/β-Domain, β-barrel, C-terminal arm), the Ku70 subunit dimerizes with the Ku80 subunit to form the protein. Unlike other DNA binding proteins, the Ku protein is asymmetrical from the differences between the Ku70 and Ku80 subunits. This asymmetry leads to different favorable locations for DNA based on major and minor grooves. The Ku70 subunit is angled closer to DNA at the double strand break, providing protectiion and interaction with its domains. In contrast, the Ku80 subunit associates with DNA away from the free end. Once a homodimer, the protein has diverged into two domains that are now 15% similar in residues. α/β-Domain Contained inside the α/β-Domain is a Rossman fold at the N terminus that is used to bind nucleotides in DNA. In terms of protein structure, the α/β-Domain contributes little to the dimer interface between the subunits. The C terminus of the domain can be bound to other repair molecules, using α/β-Domain as a scaffold. β-barrel The domain is the main site of dimer interface, with each β-barrel being composed of seven β strands with the majority in antiparallel arrangement. The quantity of the strands lends the structures to be symmetrical. Both β-barrels in the dimer form the base of the cradle by fitting in the grooves of DNA. C-terminal arm The C-terminal arm is an α-helical domain that functions to associate with the β-barrel of the opposite subunit, with the arm stretching across the DNA helix. As a result, the C-terminal arm strengthens the cradle composed of the two β-barrels. DNA binding ring

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