Electron tomography of insect flight muscle in rigor and AMPPNP at 23 degrees C

• Published in: Journal of molecular biology Vol. 264; no. 2; pp. 279 - 301
• Main Authors: Schmitz, H, Reedy, M.C, Reedy, M.K, Tregear, R.T, Winkler, H, Taylor, K.A
• Format: Journal Article
• Language: English
• Published: England 29.11.1996
• Subjects: actin; acto-s1; adenosine 5'-[beta, gamma-imide]triphosphate; adenosine phosphates; adenosine triphosphate; Adenosine Triphosphate - analogs & derivatives; Adenylyl Imidodiphosphate - pharmacology; analogs; Animals; crossbridge conformation; flight muscles; Hemiptera - ultrastructure; Image Processing, Computer-Assisted; interactions; Lethocerus; molecular conformation; muscle fibers; Muscle Fibers, Skeletal - drug effects; Muscle Fibers, Skeletal - ultrastructure; Muscle, Skeletal - drug effects; Muscle, Skeletal - ultrastructure; myosin; Myosin Subfragments - metabolism; rigor fibers; Rigor Mortis; Temperature; three dimensional reconstruction; tomography; ultrastructure
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1006/jmbi.1996.0641

Treatment of rigor fibers of insect flight muscle (IFM) with AMPPNP at 23 degrees C causes a 70% drop in tension with little change in stiffness. In order to visualize the changes in crossbridge conformation and distribution that give rise to the mechanical response, we have produced three-dimensional reconstructions by tomography of both rigor and AMPPNP-treated muscle that do not average the repeating motifs of crossbridges, and thereby retain information on variability of crossbridge structure and distribution. Tomograms can be averaged when display of only the regular features is wanted. Tomograms of rigor IFM show double-headed lead and single-headed rear crossbridges. Tomograms of IFM treated with AMPPNP at 23 degrees C reveal many double-headed and some single-headed "lead" bridges but few crossbridges corresponding to the rear bridges of rigor. Instead, new non-rigor forms of variably angled crossbridges are found bound to actin sites not labeled with myosin heads in rigor. This indicates that the rear bridges of rigor have redistributed during the transition from rigor to the AMPPNP state, which could explain the maintenance of rigor stiffness despite the loss of tension. Comparison of in situ crossbridges in tomograms of rigor with atomic model of acto-S1, the complex formed by myosin subfragment 1 and actin, reveals that the regulatory domain of S1 would require significant bending and realignment to fit into both types of rigor crossbridges. The modifications are particularly significant for the rear bridges and suggest that differential strain in the regulatory domain of rear bridges may be the basis for their detachment and redistribution upon binding AMPPNP. Similar comparison using lead-type crossbridges in AMPPNP reveals departures from the rigor acto-S1 atomic, model that include azimuthal straightening and a slight M-ward bending in the regulatory domain. Both the motor and regulatory domains of the new non-rigor crossbridges differ from those in the atomic model of acto-S1. A new crossbridge motif identified in AMPPNP-treated muscle consists of paired rigor-like and non-rigor crossbridges and suggests possible transitions in the myosin working stroke.