Insect Flight Muscle Research Articles

Selection despite low genetic diversity and high gene flow in a rapid island invasion of the bumblebee, Bombus terrestris.

Invasive species are predicted to adjust their morphological, physiological and life-history traits to adapt to their non-native environments. Although a loss of genetic variation during invasion may restrict local adaptation, introduced species often thrive in novel environments. Despite being founded by just a few individuals, Bombus terrestris (Hymenoptera: Apidae) has in less than 30 years successfully spread across the island of Tasmania (Australia), becoming abundant and competitive with native pollinators. We use RADseq to investigate what neutral and adaptive genetic processes associated with environmental and morphological variation allow B. terrestris to thrive as an invasive species in Tasmania. Given the widespread abundance of B. terrestris, we expected little genetic structure across Tasmania and weak signatures of environmental and morphological selection. We found high gene flow with low genetic diversity, although with significant isolation-by-distance and spatial variation in effective migration rates. Restricted migration was evident across the mid-central region of Tasmania, corresponding to higher elevations, pastural land, low wind speeds and low precipitation seasonality. Tajima's D indicated a recent population expansion extending from the south to the north of the island. Selection signatures were found for loci in relation to precipitation, wind speed and wing loading. Candidate loci were annotated to genes with functions related to cuticle water retention and insect flight muscle stability. Understanding how a genetically impoverished invasive bumblebee has rapidly adapted to a novel island environment provides further understanding about the evolutionary processes that determine successful insect invasions, and the potential for invasive hymenopteran pollinators to spread globally.

Glu-rich N-terminal variable region of troponin T functions as a myofilament Ca2+-reservoir to reduce SR Ca2+-cycling.

The long Glu-rich N-terminal segment of avian pectoral muscle troponin T (TnT) and C-terminal extension of insect TnT are multi-valent Ca2+-binding sites with physiologically relevant affinities. Genetic deletion of the Glu-rich C-terminal extension of insect TnT decreases muscle and heart functions but increases the tolerance of cardiomyocytes to Ca2+ overloading, indicating decreased [Ca2+]i. In contrast, cardiomyocytes from gene-edited mice expressing modified cardiac TnT with N-terminal variable region replaced by a C-terminal segment of insect TnT (51E-cTnT) show higher shortening amplitude and contraction and relaxation velocities than that of wild type (WT) control. Isolated 51E-cTnT cardiomyocytes exhibited shorter resting sarcomeres, which can be corrected by inhibiting myosin ATPase, indicating increased resting [Ca2+]i. A similar gain-of-function model,fast skeletal muscle TnTgene-edited mice with the N-terminal variable region replaced by the N-terminal segment of adult turkey pectoral muscle TnT (Tx9-fsTnT), shows normal baseline muscle functions but slower and less rising of contractile force during caffeine-induced Ca2+ release from sarcoplasmic reticulum (SR) than that of WT control, indicating a decreased SR Ca2+ store. Consistently, 51E-cTnT mouse hearts respond to beta-adrenergic stimulation or Ca2+ agonist with higher than WT ventricular peak pressure and diastolic velocity. The data support a hypothesis that the Glu-rich segments of insect and avian flight muscle TnT function as myofilament Ca2+ reservoirs to tune muscle kinetics and reduce the amount of Ca2+ cycled during contraction and relaxation. The functional effects are prominent in heterozygotes of the genetically modified flies and mice whereas the loss-of-function in Drosophila TnT and gain-of-function in 51E-cTnT and Tx9-fsTnT mice both produced homozygote lethality, indicating sensitive dose effects of the myofilament Ca2+ reservoir for use as a potent mechanism to improve energetic efficiency of cardiac and skeletal muscles.

Cryo-EM structure of tarantula myosin filament: Implications for analysis of myopathy mutations.

The high-resolution structure of myosin thick filaments of invertebrates has aided understanding of key muscle functions and analysis of disease mutations in humans. We previously published a low-resolution tarantula skeletal thick filament cryo-EM structure (Woodhead et al., 2005), which was used to map hypertrophic and dilated cardiomyopathy mutations (Alamo et al., 2017, Nag et al., 2017), present mostly in the head-head and head-tail interaction sites of the interacting-heads motif (IHM). This study suggested that the myosin coiled-coil tails in the filament backbone were arranged in groups of three, forming 40-Å-diameter subfilaments (Wray, 1979), but it lacked the detail required to resolve individual tails and to map the 40% of myopathy mutations that occur in the tail region of the molecule. Here we report a 5.5 Å resolution cryo-EM map of the tarantula thick filament backbone that resolves the densities of the full length of the myosin tails and their packing interactions. The map reveals that the tails do not form subfilaments but are arranged individually in layers forming a “molecular crystal,” in which the myosin coiled-coils gradually move towards the center of the filament, near the paramyosin core, while slowly curving around the filament axis. A similar arrangement was found in insect flight muscle thick filaments (Hu et al., 2016), suggesting it could be a general packing scheme in thick filaments, as originally proposed by Squire (1973). The positions of skip residues predict longer pitch regions and bending of the coiled-coils, as seen in the cryo-EM density. The structure also suggests new interactions of the blocked-head converter region with the backbone of the filament, implying hyperstability of IHMs. Improved resolution, and solution of the vertebrate thick filament structure, should enable precise mapping of tail mutations.

A thermodynamically consistent monte carlo cross-bridge model with a trapping mechanism reveals the role of stretch activation in heart pumping.

Changes in intracellular calcium concentrations regulate heart beats. However, the decline in the left ventricular pressure during early diastole is much sharper than that of the Ca2+ transient, resulting in a rapid supply of blood to the left ventricle during the diastole. At the tissue level, cardiac muscles have a distinct characteristic, known as stretch activation, similar to the function of insect flight muscles. Stretch activation, which is a delayed increase in force following a rapid muscle length increase, has been thought to be related to autonomous control in these muscles. In this numerical simulation study, we introduced a molecular mechanism of stretch activation and investigated the role of this mechanism in the pumping function of the heart, using the previously developed coupling multiple-step active stiffness integration scheme for a Monte Carlo (MC) cross-bridge model and a bi-ventricular finite element model. In the MC cross-bridge model, we introduced a mechanism for trapping the myosin molecule in its post-power stroke state. We then determined the rate constants of transitions for trapping and escaping in a thermodynamically consistent manner. Based on our numerical analysis, we draw the following conclusions regarding the stretch activation mechanism: (i) the delayed force becomes larger than the original isometric force because the population of trapped myosin molecules and their average force increase after stretching; (ii) the delayed force has a duration of more than a few seconds owing to a fairly small rate constant of escape from the trapped state. For the role of stretch activation in heart pumping, we draw the following conclusions: (iii) for the regions in which the contraction force decreases earlier than the neighboring region in the end-systole phase, the trapped myosin molecules prevent further lengthening of the myocytes, which then prevents further shortening of neighboring myocytes; (iv) as a result, the contraction forces are sustained longer, resulting in a larger blood ejection, and their degeneration is synchronized.

Liquid-amplified zipping actuators for micro-air vehicles with transmission-free flapping.

Flapping micro-air vehicles (MAVs) can access a wide range of locations, including confined spaces such as the inside of industrial plants and collapsed buildings, and offer high maneuverability and tolerance to disturbances. However, current flapping MAVs require transmission systems between their actuators and wings, which introduce energetic losses and additional mass, hindering performance. Here, we introduce a high-performance electrostatic flapping actuation system, the liquid-amplified zipping actuator (LAZA), which induces wing movement by direct application of liquid-amplified electrostatic forces at the wing root, eliminating the requirement of any transmission system and their associated downsides. The LAZA allows for accurate control of flapping frequency and amplitude, exhibits no variation in performance over more than 1 million actuation cycles, and delivers peak and average specific powers of 200 and 124 watts per kilogram, respectively, exceeding mammalian and insect flight muscle and on par with modern flapping MAV actuation systems. The inclusion of 50-millimeter-long passively pitching wings in a dragonfly-sized LAZA flapping system allowed the rectification of net directional thrust up to 5.73 millinewtons. This thrust was achieved while consuming only 243 milliwatts of electrical power, implying a thrust-to-power ratio of 23.6 newtons per kilowatt, similar to state-of-the-art flapping MAVs, helicopter rotors, and commercial drone motors. Last, a horizontally moving LAZA flapping system supported by a taut nylon wire was able to accelerate from at-rest and travel at speeds up to 0.71 meters per second. The LAZA enables lightweight, high-performance transmission-free flapping MAVs for long-term remote exploration and search-and-rescue missions.

A mechanism for sarcomere breathing: volume change and advective flow within the myofilament lattice

During muscle contraction, myosin motors anchored to thick filaments bind to and slide actin thin filaments. These motors rely on energy derived from ATP, supplied, in part, by diffusion from the sarcoplasm to the interior of the lattice of actin and myosin filaments. The radial spacing of filaments in this lattice may change or remain constant during contraction. If the lattice is isovolumetric, it must expand when the muscle shortens. If, however, the spacing is constant or has a different pattern of axial and radial motion, then the lattice changes volume during contraction, driving fluid motion and assisting in the transport of molecules between the contractile lattice and the surrounding intracellular space. We first create an advective-diffusive-reaction flow model and show that the flow into and out of the sarcomere lattice would be significant in the absence of lattice expansion. Advective transport coupled to diffusion has the potential to substantially enhance metabolite exchange within the crowded sarcomere. Using time-resolved x-ray diffraction of contracting muscle, we next show that the contractile lattice is neither isovolumetric nor constant in spacing. Instead, lattice spacing is time varying, depends on activation, and can manifest as an effective time-varying Poisson ratio. The resulting fluid flow in the sarcomere lattice of synchronous insect flight muscles is even greater than expected for constant lattice spacing conditions. Lattice spacing depends on a variety of factors that produce radial force, including cross-bridges, titin-like molecules, and other structural proteins. Volume change and advective transport varies with the phase of muscle stimulation during periodic contraction but remains significant at all conditions. Although varying in magnitude, advective transport will occur in all cases in which the sarcomere is not isovolumetric. Akin to “breathing,” advective-diffusive transport in sarcomeres is sufficient to promote metabolite exchange and may play a role in the regulation of contraction itself.

Mechanisms of Frank-Starling law of the heart and stretch activation in striated muscles may have a common molecular origin.

Vertebrate cardiac muscle generates progressively larger systolic force when the end diastolic chamber volume is increased, a property called the "Frank-Starling Law", or "length dependent activation (LDA)". In this mechanism a larger force develops when the sarcomere length (SL) increased, and the overlap between thick and thin filament decreases, indicating increased production of force per unit length of the overlap. To account for this phenomenon at the molecular level, we examined several hypotheses: as the muscle length is increased, (1) lattice spacing decreases, (2) Ca2+ sensitivity increases, (3) titin mediated rearrangement of myosin heads to facilitate actomyosin interaction, (4) increased SL activates cross-bridges (CBs) in the super relaxed state, (5) increased series stiffness at longer SL promotes larger elementary force/CB to account for LDA, and (6) stretch activation (SA) observed in insect muscles and LDA in vertebrate muscles may have similar mechanisms. SA is also known as delayed tension or oscillatory work, and universally observed among insect flight muscles, as well as in vertebrate skeletal and cardiacmuscles. The sarcomere stiffness observed in relaxed muscles may significantly contributes to the mechanisms of LDA. In vertebrate striated muscles, the sarcomere stiffness is mainly caused by titin, a single filamentary protein spanning from Z-line to M-line and tightly associated with the myosin thick filament. In insect flight muscles, kettin connects Z-line and the thick filament to stabilize the sarcomere structure. In vertebrate cardiac muscles, titin plays a similar role, and may account for LDA and may constitute a molecular mechanism of Frank-Starling response.

Mechanical Permeabilization as a New Method for Assessment of Mitochondrial Function in Insect Tissues.

Respirometry analysis is an effective technique to assess mitochondrial physiology. Insects are valuable biochemical models to understand metabolism and human diseases. Insect flight muscle and brain have been extensively used to explore mitochondrial function due to dissection feasibility and the low sample effort to allow oxygen consumption measurements. However, adequate plasma membrane permeabilization is required for substrates/modulators to reach mitochondria. Here, we describe a new method for study of mitochondrial physiology in insect tissues based on mechanical permeabilization as a fast and reliable method that do not require the use of detergents for chemical permeabilization of plasma membrane, while preserves mitochondrial integrity.

Making waves: A proposed new role for myosin-binding protein C in regulating oscillatory contractions in vertebrate striated muscle.

Myosin-binding protein C (MyBP-C) is a critical regulator of muscle performance that was first identified through its strong binding interactions with myosin, the force-generating protein of muscle. Almost simultaneously with its discovery, MyBP-C was soon found to bind to actin, the physiological catalyst for myosin's activity. However, the two observations posed an apparent paradox, in part because interactions of MyBP-C with myosin were on the thick filament, whereas MyBP-C interactions with actin were on the thin filament. Despite the intervening decades since these initial discoveries, it is only recently that the dual binding modes of MyBP-C are becoming reconciled in models that place MyBP-C at a central position between actin and myosin, where MyBP-C alternately stabilizes a newly discovered super-relaxed state (SRX) of myosin on thick filaments in resting muscle and then prolongs the "on" state of actin on thin filaments in active muscle. Recognition of these dual, alternating functions of MyBP-C reveals how it is central to the regulation of both muscle contraction and relaxation. The purpose of this Viewpoint is to briefly summarize the roles of MyBP-C in binding to myosin and actin and then to highlight a possible new role for MyBP-C in inducing and damping oscillatory waves of contraction and relaxation. Because the contractile waves bear similarity to cycles of contraction and relaxation in insect flight muscles, which evolved for fast, energetically efficient contraction, the ability of MyBP-C to damp so-called spontaneous oscillatory contractions (SPOCs) has broad implications for previously unrecognized regulatory mechanisms in vertebrate striated muscle. While the molecular mechanisms by which MyBP-C can function as a wave maker or a wave breaker are just beginning to be explored, it is likely that MyBP-C dual interactions with both myosin and actin will continue to be important for understanding the new functions of this enigmatic protein.

Evolution of Flight Muscle Contractility and Energetic Efficiency.

The powered flight of animals requires efficient and sustainable contractions of the wing muscles of various flying species. Despite their high degree of phylogenetic divergence, flight muscles in insects and vertebrates are striated muscles with similarly specialized sarcomeric structure and basic mechanisms of contraction and relaxation. Comparative studies examining flight muscles together with other striated muscles can provide valuable insights into the fundamental mechanisms of muscle contraction and energetic efficiency. Here, we conducted a literature review and data mining to investigate the independent emergence and evolution of flight muscles in insects, birds, and bats, and the likely molecular basis of their contractile features and energetic efficiency. Bird and bat flight muscles have different metabolic rates that reflect differences in energetic efficiencies while having similar contractile machinery that is under the selection of similar natural environments. The significantly lower efficiency of insect flight muscles along with minimized energy expenditure in Ca2+ handling is discussed as a potential mechanism to increase the efficiency of mammalian striated muscles. A better understanding of the molecular evolution of myofilament proteins in the context of physiological functions of invertebrate and vertebrate flight muscles can help explore novel approaches to enhance the performance and efficiency of skeletal and cardiac muscles for the improvement of human health.

Thick Filament Activation and Post-Tetanic Potentiation Mechanisms Evolved Differently in Invertebrate and Vertebrate Striated Muscle

Striated muscle contraction involves sliding of actin thin filaments along myosin thick filaments, controlled by calcium through thin filament activation. In relaxation, the two heads of myosin interact with each other to form the interacting-heads motif, consisting of blocked and free heads helically arranged around the filament backbone. A key question is how both free and blocked heads are activated and released from the backbone to approach actin and produce force. In a proposed mechanosensing mechanism for vertebrate striated muscle, a ∼1.4% backbone elongation leads to thick filament activation. We used time-resolved synchrotron X-ray diffraction to determine whether a similar mechanism is present in tarantula striated muscle. Tetanic isometric contraction produced only very small backbone elongation (∼0.27%), much smaller than in frog, suggesting that a mechanosensing mechanism is not of primary importance in tarantula. Rather, thick filament activation is produced by a phosphorylation mechanism, revealed by the X-ray diffraction patterns and force measurements before and after tetanus, correlated with the levels of myosin regulatory light chain phosphorylation. The results provide insights into the mechanism of force potentiation and post-tetanic potentiation. We also show that tarantula (Aphonopelma hentzi) muscle has an additional thermosensing mechanism that disorders the myosin heads above and below 22.5° C. Together, these findings suggest that -apart from insect flight muscle stretch activation - two other molecular mechanisms for thick filament activation have evolved to disrupt the intermolecular interactions that establish the relaxed helices of free and blocked heads: one in invertebrates (with a rigid paramyosin core), by either RLC phosphorylation (as in arthropods) or Ca2+-binding (as in mollusks, that lack phosphorylation), and another in vertebrates (lacking paramyosin), by mechanosensing. Supported by NIH grants AR067279, GM103622, AR072036 and HL139883.

Tropomyosin as a Stretch Sensor in the Troponin Bridges of Insect Flight Muscle

The flight muscles of many insects contract at high frequency and nearly constant concentrations of calcium. The fibres are activated by rapid stretches, and bridges between thick and thin filaments have been identified as possible stretch sensors. The bridges are spaced at 38.7 nm at the position of troponin on the thin filament, alternating with force-producing crossbridges at target sites in actin. The tropomyosin-troponin complex (Tm-Tn) in Lethocerus flight muscle has two isoforms of tropomyosin (Tm1 and Tm2). Tm-Tn and Tm1 bind to thick filaments or myosin, whereas Tm2 does not. The Tm isoforms exist as homodimers in situ and could act independently: Tm1 forming part of a Tn bridge and Tm2 acting as conventional Tm. Electron micrographs of Tm-Tn incubated with isolated thick filaments showed the complex following the helical arrangement of myosin molecules, with projections every ∼40 nm. Thick filaments were sometimes crosslinked by Tm-Tn or by Tm1 alone. Atomic force microscopy (AFM) of thick filaments in relaxing buffer showed crossbridge crowns every ∼43 nm that were ∼30 nm in height above the mica surface, and intermediate crowns ∼19 nm above the surface. The higher crowns would be more likely to interact with Tm-Tn on thin filaments. Thick filaments crosslinked by Tm1 were also observed by tapping mode AFM. Direct binding of Tm1 to myosin confirms the suggestion that non-force producing crossbridges could activate the thin filament directly when fibres are stretched, pulling Tm from an inhibitory position on actin every cycle of oscillatory contraction, without changes in calcium concentration. We will describe the differences in biophysical properties of Tm1 and Tm2.

Sub-maximally Activated Rat Soleus Fibers Exhibit Stretch Activation

Stretch activation occurs when a muscle develops force after an imposed stretch. The effect is large in some types of insect flight muscle and is also thought to contribute to cardiac function. The potential role of stretch activation in mammalian skeletal muscle is less clear. We activated chemically permeabilized rat soleus fibers in solutions with pCa values (=log10[Ca2+]) ranging from 9.0 to 4.5 and imposed ramp and hold length changes of different sizes (0.002 to 0.07 muscle lengths) and different stretch velocities (0.07 to 1.40 muscle lengths per second). All experiments were performed at 22C. When fibers were stretched in pCa 9.0 solution, force increased linearly during the stretch and decayed during the hold portion of the trial. This is consistent with the behavior of a simple visco-elastic system. Fibers immersed in solutions with pCa values between 6.6 and 6.0 exhibited more complex properties. During the stretch, the force response was biphasic due to the muscle's short-range stiffness. Immediately after the stretch, force dropped transiently, and then rose to a peak value of up to 130% of the pre-stretch isometric force. This is stretch activation. The peak stretch activated force increased with the magnitude of the stretch but was not markedly changed by stretch velocity. Fibers immersed in solutions with pCa values less than 6.0 exhibited a short-range stiffness but force declined during the hold portion of the trial and did not exhibit a delayed activation. Our measurements demonstrate that mammalian skeletal muscle can exhibit prominent stretch activation in solutions with sub-maximal calcium concentrations. To investigate the mechanisms responsible for stretch activation, we ran preliminary simulations using the MyoSim model of dynamically coupled myofilaments. These calculations suggest that force-dependent recruitment from the myosin OFF state may contribute to stretch activation.

Phote-HrTH (Phormia terraenovae Hypertrehalosaemic Hormone), the Metabolic Hormone of the Fruit Fly: Solution Structure and Receptor Binding Model

Fruit flies are a widely distributed pest insect that pose a significant threat to food security. Flight is essential for the dispersal of the adult flies to find new food sources and ideal breeding spots. The supply of metabolic fuel to power the flight muscles of insects is regulated by adipokinetic hormones (AKHs). The fruit fly, Drosophila melanogaster, has the same AKH that is present in the blowfly, Phormia terraenovae; this AKH has the code-name Phote-HrTH. Binding of the AKH to the extra-cellular binding site of a G protein-coupled receptor causes its activation. In this paper, the structure of Phote-HrTH in sodium dodecyl sulfate (SDS) micelle solution was determined using NMR restrained molecular dynamics. The peptide was found to bind to the micelle and be fairly rigid, with an S2 order parameter of 0.96. The translated protein sequence of the AKH receptor from the fruit fly, D. melanogaster, Drome-AKHR, was used to construct two models of the receptor. It is proposed that these two models represent the active and inactive state of the receptor. The model based on the crystal structure of the β-2 adrenergic receptor was found to bind Phote-HrTH with a binding constant of −102kJmol−1, while the other model, based on the crystal structure of rhodopsin, did not bind the peptide. Under molecular dynamic simulation, in a palmitoyloleoylphosphatidylcholine (POPC) membrane, the receptor complex changed from an inactive to an active state. The identification and characterisation of the ligand binding site of Drome-AKHR provide novel information of ligand–receptor interaction, which could lead to the development of species-specific control substances to use discriminately against the fruit fly.

Host plant defense produces species-specific alterations to flight muscle protein structure and flight-related fitness traits of two armyworms.

Insects manifest phenotypic plasticity in their development and behavior in response to plant defenses, via molecular mechanisms that produce tissue-specific changes. Phenotypic changes might vary between species that differ in their preferred hosts and these effects could extend beyond larval stages. To test this, we manipulated the diet of southern armyworm (SAW; Spodoptera eridania) and fall armyworm (FAW; Spodoptera frugiperda) using a tomato mutant for jasmonic acid plant defense pathway (def1), and wild-type plants, and then quantified gene expression of Troponin t (Tnt) and flight muscle metabolism of the adult insects. Differences in Tnt spliceform ratios in insect flight muscles correlate with changes to flight muscle metabolism and flight muscle output. We found that SAW adults reared on induced def1 plants had a higher relative abundance (RA) of the A isoform of Troponin t (Tnt A) in their flight muscles; in contrast, FAW adults reared on induced def1 plants had a lower RA of Tnt A in their flight muscles compared with adults reared on def1 and controls. Although mass-adjusted flight metabolic rate showed no independent host plant effects in either species, higher flight metabolic rates in SAW correlated with increased RA of Tnt A Flight muscle metabolism also showed an interaction of host plants with Tnt A in both species, suggesting that host plants might be influencing flight muscle metabolic output by altering Tnt This study illustrates how insects respond to variation in host plant chemical defense by phenotypic modifications to their flight muscle proteins, with possible implications for dispersal.

The Aerodynamics and Power Requirements of Forward Flapping Flight in the Mango Stem Borer Beetle (Batocera rufomaculata).

The need for long dispersal flights can drive selection for behavioral, physiological, and biomechanical mechanisms to reduce the energy spent flying. However, some energy loss during the transfer of momentum from the wing to the fluid is inevitable, and inherent to the fluid-wing interaction. Here, we analyzed these losses during the forward flight of the mango stem borer (Batocera rufomaculata). This relatively large beetle can disperse substantial distances in search of new host trees, and laboratory experiments have demonstrated continuous tethered flights that can last for up to an hour. We flew the beetles tethered in a wind tunnel and used high-speed videography to estimate the aerodynamic power from their flapping kinematics and particle image velocimetry (PIV) to evaluate drag and kinetic energy from their unsteady wakes. To account for tethering effects, we measured the forces applied by the beetles on the tether arm holding them in place. The drag of the flying beetle over the flapping cycle, estimated from the flow fields in the unsteady wake, showed good agreement with direct measurement of mean horizontal force. Both measurements showed that total drag during flight is ∼5-fold higher than the parasite drag on the body. The aerodynamic power estimated from both the motion of the wings, using a quasi-steady blade-element model, and the kinetic energy in the wake, gave mean values of flight-muscle mass-specific power of 87 and 65 W kg muscle-1, respectively. A comparison of the two values suggests that ∼25% of the energy is lost within the fluid due to turbulence and heat. The muscle mass-specific power found here is low relative to the maximal power output reported for insect flight muscles. This can be attributed to reduce weight support during tethered flight or to operation at submaximal output that may ensure a supply of metabolic substrates to the flight muscles, thus delaying their fatigue during long-distance flights.

A myosin-based mechanism for stretch activation and its possible role revealed by varying phosphate concentration in fast and slow mouse skeletal muscle fibers.

Stretch activation (SA) is a delayed increase in force following a rapid muscle length increase. SA is best known for its role in asynchronous insect flight muscle, where it has replaced calcium's typical role of modulating muscle force levels during a contraction cycle. SA also occurs in mammalian skeletal muscle but has previously been thought to be too low in magnitude, relative to calcium-activated (CA) force, to be a significant contributor to force generation during locomotion. To test this supposition, we compared SA and CA force at different Pi concentrations (0-16 mM) in skinned mouse soleus (slow-twitch) and extensor digitorum longus (EDL; fast-twitch) muscle fibers. CA isometric force decreased similarly in both muscles with increasing Pi, as expected. SA force decreased with Pi in EDL (40%), leaving the SA to CA force ratio relatively constant across Pi concentrations (17-25%). In contrast, SA force increased in soleus (42%), causing a quadrupling of the SA to CA force ratio, from 11% at 0 mM Pi to 43% at 16 mM Pi, showing that SA is a significant force modulator in slow-twitch mammalian fibers. This modulation would be most prominent during prolonged muscle use, which increases Pi concentration and impairs calcium cycling. Based upon our previous Drosophila myosin isoform studies and this work, we propose that in slow-twitch fibers a rapid stretch in the presence of Pi reverses myosin's power stroke, enabling quick rebinding to actin and enhanced force production, while in fast-twitch fibers, stretch and Pi cause myosin to detach from actin.

The Interacting Head Motif Structure Does Not Explain the X-Ray Diffraction Patterns in Relaxed Vertebrate (Bony Fish) Skeletal Muscle and Insect (Lethocerus) Flight Muscle.

Unlike electron microscopy, which can achieve very high resolution but to date can only be used to study static structures, time-resolved X-ray diffraction from contracting muscles can, in principle, be used to follow the molecular movements involved in force generation on a millisecond timescale, albeit at moderate resolution. However, previous X-ray diffraction studies of resting muscles have come up with structures for the head arrangements in resting myosin filaments that are different from the apparently ubiquitous interacting head motif (IHM) structures found by single particle analysis of electron micrographs of isolated myosin filaments from a variety of muscle types. This head organization is supposed to represent the super-relaxed state of the myosin filaments where adenosine triphosphate (ATP) usage is minimized. Here we have tested whether the interacting head motif structures will satisfactorily explain the observed low-angle X-ray diffraction patterns from resting vertebrate (bony fish) and invertebrate (insect flight) muscles. We find that the interacting head motif does not, in fact, explain what is observed. Previous X-ray models fit the observations much better. We conclude that the X-ray diffraction evidence has been well interpreted in the past and that there is more than one ordered myosin head state in resting muscle. There is, therefore, no reason to question some of the previous X-ray diffraction results on myosin filaments; time-resolved X-ray diffraction should be a reliable way to follow crossbridge action in active muscle and may be one of the few ways to visualise the molecular changes in myosin heads on a millisecond timescale as force is actually produced.

Effect of myofibril passive elastic properties on the mechanical communication between motor proteins on adjacent sarcomeres

Rapid sarcomere lengthening waves propagate along a single muscle myofibril during spontaneous oscillatory contraction (SPOC). In asynchronous insect flight muscles, SPOC is thought to be almost completely synchronized over the entire myofibril. This phenomenon does not require Ca2+ regulation of the dynamics of the motor proteins, and cannot be explained simply by the longitudinal mechanical equilibrium among sarcomeres in the myofibril. In the present study, we rationalize these phenomena by considering the lateral mechanical equilibrium, in which two tensions originating from the inverse relationship between sarcomere length and lattice spacing, along with the lattice alignment, play important roles in the mechanical communication between motor proteins on adjacent filaments via the Z-disc. The proposed model is capable of explaining various SPOC phenomena based on the stochastic power-stroke mechanism of motor proteins, which responds to temporal changes in longitudinal mechanical load.

Through thick and thin: dual regulation of insect flight muscle and cardiac muscle compared

Both insect flight muscle and cardiac muscle contract rhythmically, but the way in which repetitive contractions are controlled is different in the two types of muscle. We have compared the flight muscle of the water bug, Lethocerus, with cardiac muscle. Both have relatively high resting elasticity and are activated by an increase in sarcomere length or a quick stretch. The larger response of flight muscle is attributed to the highly ordered lattice of thick and thin filaments and to an isoform of troponin C that has no exchangeable Ca2+-binding site. The Ca2+ sensitivity of cardiac muscle and flight muscle can be manipulated so that cardiac muscle responds to Ca2+ like flight muscle, and flight muscle responds like cardiac muscle, showing the malleability of regulation. The interactions of the subunits in flight muscle troponin are described; a model of the complex, using the structure of cardiac troponin as a template, shows an overall similarity of cardiac and flight muscle troponin complexes. The dual regulation by thick and thin filaments in skeletal and cardiac muscle is thought to operate in flight muscle. The structure of inhibited myosin heads folded back on the thick filament in relaxed Lethocerus fibres has not been seen in other species and may be an adaptation to the rapid contractions of flight muscle. A scheme for regulation by thick and thin filaments during oscillatory contraction is described. Cardiac and flight muscle have much in common, but the differing mechanical requirements mean that regulation by both thick and thin filaments is adapted to the particular muscle.