The seven-spanning calcium-sensing receptor (CaSR) activates multiple G proteins including Gq and Gi, and thereby activates a variety of second messengers and inhibits parathyroid hormone (PTH) secretion. However, the exact signaling mechanisms underlying the functional activity of CaSR are not yet fully understood. The heterozygous inactivation of CaSR or its inhibition by antibody blocking results in either familial hypocalciuric hypercalcemia or acquired hypocalciuric hypercalcemia (AHH), respectively. Here, we report the identification of a unique CaSR autoantibody in an AHH patient. Paradoxically, we find that this autoantibody potentiates the Ca 2؉ /Gq-dependent accumulation of inositol phosphates by slightly shifting the dose dependence curve of the Ca 2؉ mediated activation of phosphatidylinositol turnover to the left, whereas it inhibits the Ca 2؉ /Gi-dependent phosphorylation of ERK1/2 in HEK293 cells stably expressing human CaSR. Treatment of these same cells with a calcimimetic, NPS-R-568, augments the CaSR response to Ca 2؉ , increasing phosphatidylinositol turnover and ERK1/2 phosphorylation, and overcoming the autoantibody effects. Our observations thus indicate that a calcium-stimulated CaSR primed by a specific autoantibody adopts a unique conformation that activates Gq but not Gi. Our findings also suggest that CaSR signaling may act via both Gq and Gi to inhibit PTH secretion. This is the first report of a disease-related autoantibody that functions as an allosteric modulator and maintains G proteincoupled receptors (GPCRs) in a unique active conformation with its agonist. We thus speculate that physiological modulators may exist that enable an agonist to specifically activate only one signaling pathway via a GPCR that activates multiple signaling pathways.allosteric modulation ͉ disease ͉ functional selectivity ͉ G protein-coupled receptors ͉ multiple active conformations

Development of preprogrammable conductive nanowires is a requisite for the future fabrication of nanoscale electronics based on molecular assembly. Here, we report the synthesis of conductive metal nanowires from nucleoprotein filaments, complexes of single- or double-stranded DNA and RecA protein. A genetically engineered RecA derivative possessing a reactive and surface accessible cysteine residue was reacted with functionalized gold particles, resulting in nucleoprotein filaments with gold particles attached. The template-based gold particles were enlarged by chemical deposition to form uniformly metallized nanowires. The programming information can be encoded in DNA sequences so that an intricate electrical circuit can be constructed through self-assembly of each component. As the RecA filament has higher degree of stiffness than double-stranded DNA, it provides a robust scaffold that allows us to fabricate more reliable and well-organized electrical circuitry at the nanoscale. Furthermore, the function of homologous pairing provides sequence-specific junction formation as well as sequence-specific patterning metallization.

Abstract. In order to reduce uncertainty in the estimation of Direct Aerosol Radiative Forcing (DARF), it is important to improve the estimation of the single scattering albedo (SSA). In this study, we propose a new data processing method to improve SSA retrievals for the SKYNET sky radiometer network, which is one of the growing number of networks of sun-sky photometers, such as NASA AERONET and others. There are several reports that SSA values from SKYNET have a bias compared to those from AERONET, which is regarded to be the most accurate due to its rigorous calibration routines and data quality and cloud screening algorithms. We investigated possible causes of errors in SSA that might explain the known biases through sensitivity experiments using a numerical model, and also using real data at the SKYNET sites at Pune (18.616 • N/73.800 • E) in India and Beijing (39.586 • N/116.229 • E) in China. Sensitivity experiments showed that an uncertainty of the order of ±0.03 in the SSA value can be caused by a possible error in the ground surface albedo or solid view angle assumed for each observation site. Another candidate for possible error in the SSA was found in cirrus contamination generated by imperfect cloud screening in the SKYNET data processing. Therefore, we developed a new data quality control method to get rid of low quality or cloud contamination data, and we applied this method to the real observation data at the Pune site in SKYNET. After applying this method to the observation data, we were able to screen out a large amount of cirruscontaminated data and to reduce the deviation in the SSA value from that of AERONET. We then estimated DARF using data screened by our new method. The result showed that the method significantly reduced the difference of 5 W m −2 that existed between the SKYNET and AERONET values of DARF before screening. The present study also suggests the necessity of preparing suitable a priori information on the distribution of coarse particles ranging in radius between 10 µm and 30 µm for the analysis of heavily dust-laden atmospheric cases.

Pasteurella multocida toxin (PMT) is a virulence factor responsible for the pathogenesis of some Pasteurellosis. PMT exerts its toxic effects through the activation of heterotrimeric GTPase (Gq, G12/13 and Gi)‐dependent pathways, by deamidating a glutamine residue in the α subunit of these GTPases. However, the enzymatic characteristics of PMT are yet to be analyzed in detail because the deamidation has only been observed in cell‐based assays. In the present study, we developed rat monoclonal antibodies, specifically recognizing the deamidated Gαq, to detect the actions of PMT by immunological techniques such as western blotting. Using the monoclonal antibodies, we found that the toxin deamidated Gαq only under reducing conditions. The C‐terminal region of PMT, C‐PMT, was more active than the full‐length PMT. The C3 domain possessing the enzyme core catalyzed the deamidation in vitro without any other domains. These results not only support previous observations on toxicity, but also provide insights into the enzymatic nature of PMT. In addition, we present several lines of evidence that Gα11, as well as Gαq, could be a substrate for PMT.