Limited neuromuscular input results in muscle weakness in neuromuscular disease either because of a reduction in the density of muscle innervation, the rate of neuromuscular junction activation or the efficiency of synaptic transmission1. We developed a small molecule fast skeletal troponin activator, CK-2017357, as a means to increase muscle strength by amplifying the response of muscle when neuromuscular input is diminished secondary to a neuromuscular disease. Binding selectively to the fast skeletal troponin complex, CK-2017357 slows the rate of calcium release from troponin C and sensitizes muscle to calcium. As a consequence, the force-calcium relationship of muscle fibers shifts leftwards as does the force-frequency relationship of a nerve-muscle pair. In vitro and in vivo, CK-2017357 increases the production of force at sub-maximal stimulation rates. Importantly, we show that sensitization of the fast skeletal troponin complex to calcium improves muscle force and grip strength immediately after single doses of CK-2017357 in a model of neuromuscular disease, myasthenia gravis. Troponin activation may provide a new therapeutic approach to improve physical activity in diseases where neuromuscular function is compromised.

N ational Instruments LabVIEW is a graphical programming language that has its roots in automation control and data acquisition. Its graphical representation, similar to a process flow diagram, was created to provide an intuitive programming environment for scientists and engineers. The language has matured over the last 20 years to become a general purpose programming environment. LabVIEW has several key features which make it a good choice in an automation environment. These include simple network communication, turnkey implementation of common communication protocols (RS232, GPIB, etc.), powerful toolsets for process control and data fitting, fast and easy user interface construction, and an efficient code execution environment. We discuss the merits of the language and provide an example application suite written in-house which is used in integrating and controlling automation platforms.

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Fluorescence correlation spectroscopy, using tota internal reflection excitation (TIRFCS), is developed as a method to allow quantitative determination of molecular populations at solid/liquid interfaces. Population fluctuations of fluorescent molecules at the interface are observed as excess low-frequency noise on a fluorescence signal. Since the noise arises from molecular origins, its magnitude can be evaluated by Poisson statistics to determine the number of molecules in the interface volume. This quantitative information is available without sensitivity calibration or the preparation of standards and without fitting the transients to a kinetic model. Unlike single-molecule counting measurements, TIRFCS can produce these quantitative results even when the number of photoelectrons detected per molecule is small. Surface populations of rhodamine 6G dye molecules were measured at C-18-derivatized, flat silica surfaces in contact with aqueous solutions and compared with predicted values derived from chromatographic retention data. In addition, electrostatic and nonpolar contributions to the free energy of adsorption of the dye to C-18-modified silica surfaces were examined.

Atomic force microscopy (AFM) tips and glass surfaces were modified with various organosilanes to determine magnitude and dispersion information about single-molecule bond-rupture forces. X-ray photoelectron spectroscopy (XPS) and contact-angle measurements were used to study and quantify organosilane adsorption on the glass surface and on SiO2-coated AFM tips. Hydrogen bond interactions between hydroxyl- and thiol-terminated groups on the tip and surface were detected and measured. Differentiation between the functionalities of the acetate- and thioacetate-terminated silanes and their reduced forms produced by on-surface reduction (the alcohol and thiol, respectively) was also accomplished. The experiments demonstrate the complementary information that can be obtained from AFM and XPS and illustrate how they can be used to determine the nature of the surface after an organic transformation has occurred to the functional groups present. They also represent a first step in detecting chemical reactions on a localized scale and in measuring the dispersion in the single-molecule bond-rupture force when it exists.