933 research outputs found

    Structure, regulation, and function of protein tyrosine phosphatases

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    The phosphorylation of tyrosyl residues in proteins is an essential aspect of many signal transduction events, including the control of both normal and neoplastic cell growth and proliferation. Since the earliest observations of tyrosine phosphorylation, it has been appreciated that this is a reversible process in which the net level of phosphate in a target substrate reflects the balance between the competing action of kinases and phosphatases. Thus, in cells transformed by temperature-sensitive mutants of Rous sarcoma virus, an elevation in the levels of phosphotyrosine is observed at the permissive temperature, at which the kinase is active; however, if the cells are shifted to the nonpermissive temperature, at which the kinase is inactivated, a rapid dephosphorylation of tyrosyl residues ensues due to the action of protein tyrosine phosphatases (PTPases) (Sefton et al. 1980). The last 10 years has witnessed great progress in the characterization of the protein tyrosine kinases, whereas..

    A Poly-algorithmic Approach to Quantifier Elimination

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    Cylindrical Algebraic Decomposition (CAD) was the first practical means for doing real quantifier elimination (QE), and is still a major method, with many improvements since Collins' original method. Nevertheless, its complexity is inherently doubly exponential in the number of variables. Where applicable, virtual term substitution (VTS) is more effective, turning a QE problem in nn variables to one in n−1n-1 variables in one application, and so on. Hence there is scope for hybrid methods: doing VTS where possible then using CAD. This paper describes such a poly-algorithmic implementation, based on the second author's Ph.D. thesis. The version of CAD used is based on a new implementation of Lazard's recently-justified method, with some improvements to handle equational constraints

    HGF-independent regulation of MET and GAB1 by nonreceptor tyrosine kinase FER potentiates metastasis in ovarian cancer

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    Ovarian cancer cells disseminate readily within the peritoneal cavity, which promotes metastasis, and are often resistant to chemotherapy. Ovarian cancer patients tend to present with advanced disease, which also limits treatment options; consequently, new therapies are required. The oncoprotein tyrosine kinase MET, which is the receptor for hepatocyte growth factor (HGF), has been implicated in ovarian tumorigenesis and has been the subject of extensive drug development efforts. Here, we report a novel ligand- and autophosphorylation-independent activation of MET through the nonreceptor tyrosine kinase feline sarcoma-related (FER). We demonstrated that the levels of FER were elevated in ovarian cancer cell lines relative to those in immortalized normal surface epithelial cells and that suppression of FER attenuated the motility and invasive properties of these cancer cells. Furthermore, loss of FER impaired the metastasis of ovarian cancer cells in vivo. Mechanistically, we demonstrated that FER phosphorylated a signaling site in MET: Tyr1349. This enhanced activation of RAC1/PAK1 and promoted a kinase-independent scaffolding function that led to recruitment and phosphorylation of GAB1 and the specific activation of the SHP2-ERK signaling pathway. Overall, this analysis provides new insights into signaling events that underlie metastasis in ovarian cancer cells, consistent with a prometastatic role of FER and highlighting its potential as a novel therapeutic target for metastatic ovarian cancer

    Phytoseiulus persimilis (Acarina: Phytoseiidae) for control of two-spotted mites in a commercial greenhouse

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    Natural infestations of the two-spotted spider mite were controlled on green house cucumber by early releases of the predatory mite, Phytoseiulus persimilis Athias-Henriot. Later sporadic mite outbreaks severely damaged some plants and required frequent surveys and repeated predator releases in the greenhouse. However, no mite sprays were required and crop yield was satisfactory

    Three-dimensional molecular dynamics simulations of void coalescence during dynamic fracture of ductile metals

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    Void coalescence and interaction in dynamic fracture of ductile metals have been investigated using three-dimensional strain-controlled multi-million atom molecular dynamics simulations of copper. The correlated growth of two voids during the coalescence process leading to fracture is investigated, both in terms of its onset and the ensuing dynamical interactions. Void interactions are quantified through the rate of reduction of the distance between the voids, through the correlated directional growth of the voids, and through correlated shape evolution of the voids. The critical inter-void ligament distance marking the onset of coalescence is shown to be approximately one void radius based on the quantification measurements used, independent of the initial separation distance between the voids and the strain-rate of the expansion of the system. The interaction of the voids is not reflected in the volumetric asymptotic growth rate of the voids, as demonstrated here. Finally, the practice of using a single void and periodic boundary conditions to study coalescence is examined critically and shown to produce results markedly different than the coalescence of a pair of isolated voids.Comment: Accepted for publication in Physical Review

    Structure, Regulation, and Function of Protein Tyrosine Phosphatases

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