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71.
Binding of calcium to CaM exposes clefts in both N- and C-domains to promote their cooperative association with a diverse array of target proteins, functioning to relay the calcium signal regulating cellular metabolism. To clarify relationships between the calcium-dependent activation of individual domains and interdomain structural transitions associated with productive binding to target proteins, we have utilized three engineered CaM mutants that were covalently labeled with N-(1-pyrene) maleimide at introduced cysteines in the C- and N-domains, i.e., T110C (PyC-CaM), T34C (PyN-CaM), and T34C/T110C (Py2-CaM). These sites were designed to detect known conformers of CaM such that upon association with classical CaM-binding sequences, the pyrenes in Py2-CaM are brought close together, resulting in excimer formation. Complementary measurements of calcium-dependent enhancements of monomer fluorescence of PyC-CaM and PyN-CaM permit a determination of the calcium-dependent activation of individual domains and indicate the sequential calcium occupancy of the C- and N-terminal domains, with full saturation at 7.0 and 300 microM calcium, respectively. Substantial amounts of excimer formation are observed for apo-CaM prior to peptide association, indicating that interdomain interactions occur in solution. Calcium binding results in a large and highly cooperative reduction in the level of excimer formation; its calcium dependence coincides with the occupancy of C-terminal sites. These results indicate that interdomain interactions between the opposing domains of CaM occur in solution and that the occupancy of C-terminal calcium binding sites is necessary for the structural coupling between the opposing domains associated with the stabilization of the interdomain linker to enhance target protein binding. 相似文献
72.
We have used fluorescence spectroscopy to investigate the structure of calmodulin (CaM) bound with CaM-binding sequences of either the plasma membrane Ca-ATPase or the skeletal muscle ryanodine receptor (RyR1) calcium release channel. Following derivatization with N-(1-pyrene)maleimide at engineered sites (T34C and T110C) within the N- and C-domains of CaM, contact interactions between these opposing domains of CaM resulted in excimer fluorescence that permits us to monitor conformational states of bound CaM. Complementary measurements take advantage of the unique conserved Trp within CaM-binding sequences that functions as a hydrophobic anchor in CaM binding and permits measurements of both a local and global peptide structure. We find that CaM binds with high affinity in a collapsed structure to the CaM-binding sequences of both the Ca-ATPase and RyR1, resulting in excimer formation that is indicative of contact interactions between the N- and the C-domains of CaM in complex with these CaM-binding peptides. There is a 4-fold larger amount of excimer formation for CaM bound to the CaM-binding sequence of the Ca-ATPase in comparison to RyR1, indicating a closer structural coupling between CaM domains in this complex. Prior to CaM association, the CaM-binding sequences of the Ca-ATPase and RyR1 are conformationally disordered. Upon CaM association, the CaM-binding sequence of the Ca-ATPase assumes a highly ordered structure. In comparison, the CaM-binding sequence of RyR1 remains conformationally disordered irrespective of CaM binding. These results suggest an important role for interdomain contact interactions between the opposing domains of CaM in stabilizing the structure of the peptide complex. The substantially different structural responses associated with CaM binding to Ca-ATPase and RyR1 indicates a plasticity in their respective binding mechanisms that accomplishes different physical mechanisms of allosteric regulation, involving either the dissociation of a C-terminal regulatory domain necessary for pump activation or the modulation of intersubunit interactions to diminish RyR1 channel activity. 相似文献
73.
Insights into PG‐binding,conformational change,and dimerization of the OmpA C‐terminal domains from Salmonella enterica serovar Typhimurium and Borrelia burgdorferi
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Kemin Tan Brooke L. Deatherage Kaiser Ruiying Wu Marianne Cuff Yao Fan Lance Bigelow Robert P. Jedrzejczak Joshua N. Adkins John R. Cort Gyorgy Babnigg Andrzej Joachimiak 《Protein science : a publication of the Protein Society》2017,26(9):1738-1748
Salmonella enterica serovar Typhimurium can induce both humoral and cell‐mediated responses when establishing itself in the host. These responses are primarily stimulated against the lipopolysaccharide and major outer membrane (OM) proteins. OmpA is one of these major OM proteins. It comprises a N‐terminal eight‐stranded β‐barrel transmembrane domain and a C‐terminal domain (OmpACTD). The OmpACTD and its homologs are believed to bind to peptidoglycan (PG) within the periplasm, maintaining bacterial osmotic homeostasis and modulating the permeability and integrity of the OM. Here we present the first crystal structures of the OmpACTD from two pathogens: S. typhimurium (STOmpACTD) in open and closed forms and causative agent of Lyme Disease Borrelia burgdorferi (BbOmpACTD), in closed form. In the open form of STOmpACTD, an aspartate residue from a long β2‐α3 loop points into the binding pocket, suggesting that an anion group such as a carboxylate group from PG is favored at the binding site. In the closed form of STOmpACTD and in the structure of BbOmpACTD, a sulfate group from the crystallization buffer is tightly bound at the binding site. The differences between the closed and open forms of STOmpACTD, suggest a large conformational change that includes an extension of α3 helix by ordering a part of β2‐α3 loop. We propose that the sulfate anion observed in these structures mimics the carboxylate group of PG when bound to STOmpACTD suggesting PG‐anchoring mechanism. In addition, the binding of PG or a ligand mimic may enhance dimerization of STOmpACTD, or possibly that of full length STOmpA. 相似文献
74.
75.
Horace L. Barnett Fredrick L. Bergmann Catherine Short Bigelow Julia Joyce Harper Brashear Ricardo Callejas Jane Colten Fay Kenoyer Daily William A. Daily Ray Fields Dawson Thelma F. Engle Robert H. Farber Robert I. Fletcher F. Raymond Fosberg Jeanne Smith Gillum William D. Gray Mary Swan Hagen Charles B. Heiser Jerome C. Hixson James M. Koepper Marjorie H. Ladley H. Harvey Lafuze Bassett Maguire Lois Carter McClure Shirley A. Moses John W. Oswald Sally Pope Overman Value M. Poor Seth Pope Marion McBurney Rice Velva E. Rudd Richard D. Schein Kathryn Jung Schmidt Emory G. Simmons Albert C. Smith Charlotte Epple Smith Julian A. Steyermark Margaret Emily McGaughey Stoner James H. Tate Oswald Tippo Ruth E. Van Seventer Ken Wagner Winona H. Welch Howard Youse 《Brittonia》1989,41(3):236-284
Editor’s note: This tribute was prepared by Barbara Yuncker from a recorded interview she had with Dr. Callejas during his
six-week visit to the Garden’s Herbarium in September 1988 to study the Piperaceae specimens received from DePauw University. 相似文献
76.
Effect of gibberellic Acid on silica content and distribution in sugarcane 总被引:1,自引:1,他引:0
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Kaufman PB Ghosheh NS Lee M Carlson TJ Jones JD Rigot W Bigelow WC Kraus S 《Plant physiology》1981,68(2):314-317
The effect of gibberellic acid on the content and distribution of silicon in the stem, leaf sheath, and leaf lamina of sugarcane was analyzed in relation to the effect of gibberellic acid on stem growth. Silicon content was measured by neutron activation analysis, and its distribution was followed by scanning electron microscopy and X-ray analysis. 相似文献
77.
By means of electron probe analysis, the effects of significant amounts of accumulation of silicon on the accumulation of calcium, potassium, magnesium, manganese, phosphorous, iron, and sodium in the silica cells of rice leaves are described. The silica cells of both the surfaces of the leaf blade and leaf sheath were studied. Silicon accumulation in the silica cells appears to decrease the amount of accumulation of potassium on both the surfaces of the leaf blade and sheath. The effect of significant amounts of silicon accumulation on the accumulation of other elements in a particular cell varies in different organs or on different surfaces of the organ of the same plant. Magnesium, manganese, iron, and phosphorus could not be detected in the adaxial epidermis of the leaf sheath and magnesium and iron in the adaxial epidermis of the leaf blade. Manganese, magnesium, and phosphorus were not detected in the abaxial epidermis of the leaf blade nor iron in the abaxial epidermis of the leaf sheath. Sodium was not revealed in either surface of the leaf blade and leaf sheath. Possible mechanisms for the effects of silicon accumulation on the accumulation of these elements in rice leaf epidermal cells are discussed. 相似文献
78.
When urea is added to ribonuclease A that has already been denatured by salt (CaCl2, LiClO4 or LiCl were used), a second co-operative transition occurs, supporting the previous demonstration that these salts cause only partial denaturation. Also we have studied the effect of the salts on the urea denaturation, and the effect of urea on the salt denaturation. At low concentrations urea makes the salt transitions occur at lower concentrations, but at higher concentrations it changes the transition so that the completely disordered protein found in urea is produced by the salt. At low concentrations the salts actually stabilize the protein against denaturation by urea, but at higher concentrations they destabilize it. The data are presented in “phase diagrams” which are found to be very useful for such three-component systems. 相似文献
79.
A species of Labyrinthula that causes 'rapid blight' and death of turfgrass has been isolated and studied. We name this new species Labyrinthula terrestris and briefly summarize morphological characteristics and growth patterns of this pathogen of turfgrass. 相似文献
80.
Redox modulation of cellular signaling and metabolism through reversible oxidation of methionine sensors in calcium regulatory proteins 总被引:8,自引:0,他引:8
Adaptive responses associated with environmental stressors are critical to cell survival. Under conditions when cellular redox and antioxidant defenses are overwhelmed, the selective oxidation of critical methionines within selected protein sensors functions to down-regulate energy metabolism and the further generation of reactive oxygen species (ROS). Mechanistically, these functional changes within protein sensors take advantage of the helix-breaking character of methionine sulfoxide. The sensitivity of several calcium regulatory proteins to oxidative modification provides cellular sensors that link oxidative stress to cellular response and recovery. Calmodulin (CaM) is one such critical calcium regulatory protein, which is functionally sensitive to methionine oxidation. Helix destabilization resulting from the oxidation of either Met(144) or Met(145) results in the nonproductive association between CaM and target proteins. The ability of oxidized CaM to stabilize its target proteins in an inhibited state with an affinity similar to that of native (unoxidized) CaM permits this central regulatory protein to function as a cellular rheostat that down-regulates energy metabolism in response to oxidative stress. Likewise, oxidation of a methionine within a critical switch region of the regulatory protein phospholamban is expected to destabilize the phosphorylation-dependent helix formation necessary for the release of enzyme inhibition, resulting in a down-regulation of the Ca-ATPase in response to beta-adrenergic signaling in the heart. We suggest that under acute conditions, such as inflammation or ischemia, these types of mechanisms ensure minimal nonspecific cellular damage, allowing for rapid restoration of cellular function through repair of oxidized methionines by methionine sulfoxide reductases and degradation pathways after restoration of normal cellular redox conditions. 相似文献