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排序方式: 共有205条查询结果,搜索用时 203 毫秒
81.
Arvind Anand Morgan LeDoyt Carson Karanian Amit Luthra Mary Koszelak-Rosenblum Michael G. Malkowski Robbins Puthenveetil Olga Vinogradova Justin D. Radolf 《The Journal of biological chemistry》2015,290(19):12313-12331
We previously identified Treponema
pallidum
repeat proteins TprC/D, TprF, and TprI as candidate outer membrane proteins (OMPs) and subsequently demonstrated that TprC is not only a rare OMP but also forms trimers and has porin activity. We also reported that TprC contains N- and C-terminal domains (TprCN and TprCC) orthologous to regions in the major outer sheath protein (MOSPN and MOSPC) of Treponema denticola and that TprCC is solely responsible for β-barrel formation, trimerization, and porin function by the full-length protein. Herein, we show that TprI also possesses bipartite architecture, trimeric structure, and porin function and that the MOSPC-like domains of native TprC and TprI are surface-exposed in T. pallidum, whereas their MOSPN-like domains are tethered within the periplasm. TprF, which does not contain a MOSPC-like domain, lacks amphiphilicity and porin activity, adopts an extended inflexible structure, and, in T. pallidum, is tightly bound to the protoplasmic cylinder. By thermal denaturation, the MOSPN and MOSPC-like domains of TprC and TprI are highly thermostable, endowing the full-length proteins with impressive conformational stability. When expressed in Escherichia coli with PelB signal sequences, TprC and TprI localize to the outer membrane, adopting bipartite topologies, whereas TprF is periplasmic. We propose that the MOSPN-like domains enhance the structural integrity of the cell envelope by anchoring the β-barrels within the periplasm. In addition to being bona fide T. pallidum rare outer membrane proteins, TprC/D and TprI represent a new class of dual function, bipartite bacterial OMP. 相似文献
82.
Priya Luthra David S. Jordan Daisy W. Leung Gaya K. Amarasinghe Christopher F. Basler 《Journal of virology》2015,89(9):5148-5153
Ebola virus VP35 inhibits alpha/beta interferon production and functions as a viral polymerase cofactor. Previously, the 8-kDa cytoplasmic dynein light chain (LC8) was demonstrated to interact with VP35, but the functional consequences were unclear. Here we demonstrate that the interaction is direct and of high affinity and that binding stabilizes the VP35 N-terminal oligomerization domain and enhances viral RNA synthesis. Mutational analysis demonstrates that VP35 interaction is required for the functional effects of LC8. 相似文献
83.
84.
Escargot maintains stemness and suppresses differentiation in Drosophila intestinal stem cells
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85.
Ashley M. Groshong Andr A. Grassmann Amit Luthra Melissa A. McLain Anthony A. Provatas Justin D. Radolf Melissa J. Caimano 《PLoS pathogens》2021,17(7)
In this study, we examined the relationship between c-di-GMP and its only known effector protein, PlzA, in Borrelia burgdorferi during the arthropod and mammalian phases of the enzootic cycle. Using a B. burgdorferi strain expressing a plzA point mutant (plzA-R145D) unable to bind c-di-GMP, we confirmed that the protective function of PlzA in ticks is c-di-GMP-dependent. Unlike ΔplzA spirochetes, which are severely attenuated in mice, the plzA-R145D strain was fully infectious, firmly establishing that PlzA serves a c-di-GMP-independent function in mammals. Contrary to prior reports, loss of PlzA did not affect expression of RpoS or RpoS-dependent genes, which are essential for transmission, mammalian host-adaptation and murine infection. To ascertain the nature of PlzA’s c-di-GMP-independent function(s), we employed infection models using (i) host-adapted mutant spirochetes for needle inoculation of immunocompetent mice and (ii) infection of scid mice with in vitro-grown organisms. Both approaches substantially restored ΔplzA infectivity, suggesting that PlzA enables B. burgdorferi to overcome an early bottleneck to infection. Furthermore, using a Borrelia strain expressing a heterologous, constitutively active diguanylate cyclase, we demonstrate that ‘ectopic’ production of c-di-GMP in mammals abrogates spirochete virulence and interferes with RpoS function at the post-translational level in a PlzA-dependent manner. Structural modeling and SAXS analysis of liganded- and unliganded-PlzA revealed marked conformational changes that underlie its biphasic functionality. This structural plasticity likely enables PlzA to serve as a c-di-GMP biosensor that in its respective liganded and unliganded states promote vector- and host-adaptation by the Lyme disease spirochete. 相似文献
86.
Mycobacterium tuberculosis is a successful pathogen largely due to its ability to persist in humans while evading the host immune system. Rv2557 and Rv2558 are two uncharacterized proteins which have been found to be present in the human granuloma along with other important proteins like isocitrate lyase and nitric oxide reductase which are necessary for long-term persistence. The two proteins are up-regulated in in vitro carbon-starvation conditions designed to mimic the latent stage. Genes corresponding to Rv2557 and Rv2558 are found only in Mycobacterium sp. so far and share high sequence identity of 65.4% at the protein level. In the present study we have cloned and purified the proteins as part of a long-term goal to understand their functional roles and importance to the pathogen. We have probed for their biophysical properties. The proteins are monomeric and do not interact with each other as revealed by size-exclusion chromatography and pull-down assays. Circular dichroism experiments involving temperature and chemical denaturation studies demonstrate that Rv2557 is more structured compared to Rv2558, which is surprising, given the high sequence conservation between them. In fact the free energy change (DeltaG(0)) of Rv2557 during guanidium chloride induced denaturation is higher than Rv2558 indicating higher structural stability. The unfolding studies indicate that overall both proteins unfold in a cooperative two state process but adopt different modes of stabilization. The present work sets the stage for further experiments to probe the functions of the proteins. 相似文献
87.
88.
The levels of starch, soluble sugars, starch mobilizing enzymes(amylases and phosphorylase) and sodium [2-I4C] acetate incorporationinto essential oil have been examined during leaf ontogeny oflemongrass (Cymbopogon flexuosus Stapf., cv. OD-19). The degradationof starch was predominantly amylolytic and ß-amylasewas the major enzyme involved. Its activity was quite high duringthe period of active leaf growth accompanying active accumulationof essential oil. The activities of a-amylase and phosphorylasewere relatively lower. The change in starch to soluble sugarsratio was inversely related to ß-amylase activity.The time-course (12 h light followed by 12 h dark) monitoringof the [I4C]-radioactivity in starch and essential oil, afterexposure of the immature (15 days after emergence) leaf to 14CO2,revealed a progressive loss of label from starch and a parallelincrease in radioactivity in essential oil. The results havebeen discussed in relation to degradation of transitory starchserving as the source of carbon precursor for essential oil(monoterpene) biogenesis in the tissue. The amount of exogenouslysupplied acetate incorporated into essential oil increased tremendouslywith 5-10 fold decrease in specific activity of the labelledacetate (2,110 GBq mole1). The effect was largely manifestedin citral, the chief (ca. 80%) constituent oflemongrass essential oil. Ontogenetically, the amount of essentialoil synthesized from the exogenously supplied precursor (acetate)was much higher in young (10 days after emergence) than in mature(30 days after emergence) leaf. Thus, the leaf developmentalphase influences the expression of essential oil metabolismand actual synthesis. Only young lemongrass leaves are substantiallyactive to synthesize essential oil. The oil biosynthetic phaseappears to be coordinated/integrated with the development ofelevated levels of certain primary metabolic activities likestarch mobilization.
1CIMAP Publication No. 706
2Present address: CSIR Complex, Palampur-176 061, Kangra Distt.Himachal Pradesh, India
J Present address (until October 10, 1991): Department of Biology,Queen's University, Kingston, Ontario, K7L 3N6, Canada (Received November 30, 1990; Accepted May 31, 1991) 相似文献
89.
(Ca2+ + Mg2+)-ATPase activity of red cells and their isolated membranes was investigated in the presence of various Ca2+ concentrations and cytoplasmic activator protein. Red cell ATPase activity was high at low Ca2+ concentrations, and low at moderate and high concentrations of Ca2+. In the case of isolated membranes, both low and moderate ca2+ concentrations produced higher (Ca2+ + Mg2+)-ATPase activity than high Ca2+ concentration. Membrane-free hemolysate containing soluble activator of (Ca2+ + Mg2+)-ATPase produced a significant increase in (Ca2+ + Mg2+)-ATPase activity only at low ca2+ concentration. Regardless of Ca2+ and activator concentrations, the enzyme activity in the membrane was lower than lysed red cells. The low level of (Ca2+ + Mg2+)-ATPase activity seen at high Ca2+ concentration can be augmented by lowering the Ca2+ concentration of EGTA in the assay medium. However, once the membrane was exposed to a high Ca2+ concentration, the activator could no longer exert it maximum stimulation at the low Ca2+ concentration brought about by addition of EGTA. This loss of activation was not attributable to the Ca2+-induced denaturation of activator protein but rather related to the alteration of (Ca2+ + Mg2+)-ATPase states in the membrane. On the basis of these data, it is suggested that only a small portion of (Ca2+ + Mg2+)-ATPase activity of isolated membranes can be stimulated by the soluble activator and that (ca2+ + Mg2+)ATPase most likely exists in various states depending upon ca2+ concentration and the presence of activator. The enzyme state exhibiting the high degree of stimulation by activator may undergo irreversible damage in the presence of high Ca2+ concentrations. 相似文献
90.
The effect of purified calmodulin on the calcium-dependent phosphorylation of human erythrocyte membranes was studied. Under the conditions employed, only one major peak of phosphorylation was observed when solubilized membrane proteins were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The molecular weight of this phosphorylated protein band was estimated to be 130000 and in the presence of purified red blood cell calmodulin, the rate of phosphorylation of this band was increased. These data suggest that calmodulin activation of (Ca2+ + Mg2+)-ATPase could be a partial reflection of an increased rate of phosphorylation of the (Ca2+ + Mg2+)-ATPase of human erythrocyte membranes. 相似文献