Crystal Structures of Expressed Non-polymerizable Monomeric Actin in the ADP and ATP States Export

@article{citeulike:3486817, abstract = {Actin filament growth and disassembly, as well as affinity for actin-binding proteins, is mediated by the nucleotide-bound state of the component actin monomers. The structural differences between ATP-actin and ADP-actin, however, remain controversial. We expressed a cytoplasmic actin in Sf9 cells, which was rendered non-polymerizable by virtue of two point mutations in subdomain 4 (A204E/P243K). This homogeneous monomer, called AP-actin, was crystallized in the absence of toxins, binding proteins, or chemical modification, with ATP or ADP at the active site. The two surface mutations do not perturb the structure. Significant differences between the two states are confined to the active site region and sensor loop. The active site cleft remains closed in both states. Minor structural shifts propagate from the active site toward subdomain 2, but dissipate before reaching the DNase binding loop (D-loop), which remains disordered in both the ADP and ATP states. This result contrasts with previous structures of actin made monomeric by modification with tetramethylrhodamine, which show formation of an {alpha}-helix at the distal end of the D-loop in the ADP-bound but not the ATP-bound form (Otterbein, L. R., Graceffa, P., and Dominguez, R. (2001) Science 293, 708-711). Our reanalysis of the TMR-modified actin structures suggests that the nucleotide-dependent formation of the D-loop helix may result from signal propagation through crystal packing interactions. Whereas the observed nucleotide-dependent changes in the structure present significantly different surfaces on the exterior of the actin monomer, current models of the actin filament lack any actin-actin interactions that involve the region of these key structural changes. 10.1074/jbc.M601973200}, author = {Rould, Mark A. and Wan, Qun and Joel, Peteranne B. and Lowey, Susan and Trybus, Kathleen M.}, citeulike-article-id = {3486817}, citeulike-linkout-0 = {http://dx.doi.org/10.1074/jbc.M601973200}, citeulike-linkout-1 = {http://www.jbc.org/cgi/content/abstract/281/42/31909}, citeulike-linkout-2 = {http://view.ncbi.nlm.nih.gov/pubmed/16920713}, citeulike-linkout-3 = {http://www.hubmed.org/display.cgi?uids=16920713}, doi = {10.1074/jbc.M601973200}, journal = {J. Biol. Chem.}, keywords = {actin, mutant, protein, xray-crystal-structure}, month = {October}, number = {42}, pages = {31909--31919}, posted-at = {2008-11-07 08:20:33}, priority = {2}, title = {Crystal Structures of Expressed Non-polymerizable Monomeric Actin in the ADP and ATP States}, url = {http://dx.doi.org/10.1074/jbc.M601973200}, volume = {281}, year = {2006} }

TY - JOUR ID - citeulike:3486817 L3 - citeulike-article-id:3486817 N2 - Actin filament growth and disassembly, as well as affinity for actin-binding proteins, is mediated by the nucleotide-bound state of the component actin monomers. The structural differences between ATP-actin and ADP-actin, however, remain controversial. We expressed a cytoplasmic actin in Sf9 cells, which was rendered non-polymerizable by virtue of two point mutations in subdomain 4 (A204E/P243K). This homogeneous monomer, called AP-actin, was crystallized in the absence of toxins, binding proteins, or chemical modification, with ATP or ADP at the active site. The two surface mutations do not perturb the structure. Significant differences between the two states are confined to the active site region and sensor loop. The active site cleft remains closed in both states. Minor structural shifts propagate from the active site toward subdomain 2, but dissipate before reaching the DNase binding loop (D-loop), which remains disordered in both the ADP and ATP states. This result contrasts with previous structures of actin made monomeric by modification with tetramethylrhodamine, which show formation of an {alpha}-helix at the distal end of the D-loop in the ADP-bound but not the ATP-bound form (Otterbein, L. R., Graceffa, P., and Dominguez, R. (2001) Science 293, 708-711). Our reanalysis of the TMR-modified actin structures suggests that the nucleotide-dependent formation of the D-loop helix may result from signal propagation through crystal packing interactions. Whereas the observed nucleotide-dependent changes in the structure present significantly different surfaces on the exterior of the actin monomer, current models of the actin filament lack any actin-actin interactions that involve the region of these key structural changes. 10.1074/jbc.M601973200 IS - 42 JF - J. Biol. Chem. EP - 31919 TI - Crystal Structures of Expressed Non-polymerizable Monomeric Actin in the ADP and ATP States VL - 281 SP - 31909 KW - actin KW - mutant KW - protein KW - xray-crystal-structure AU - Rould, Mark AU - Wan, Qun AU - Joel, Peteranne AU - Lowey, Susan AU - Trybus, Kathleen PY - 2006/10/20/ UR - http://dx.doi.org/10.1074/jbc.M601973200 ER -