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961.
Rotundo RL Ruiz CA Marrero E Kimbell LM Rossi SG Rosenberry T Darr A Tsoulfas P 《Chemico-biological interactions》2008,175(1-3):26-29
The collagen-tailed form of acetylcholinesterase (ColQ-AChE) is the major if not unique form of the enzyme associated with the neuromuscular junction (NMJ). This enzyme form consists of catalytic and non-catalytic subunits encoded by separate genes, assembled as three enzymatic tetramers attached to the three-stranded collagen-like tail (ColQ). This synaptic form of the enzyme is tightly attached to the basal lamina associated with the glycosaminoglycan perlecan. Fasciculin-2 is a snake toxin that binds tightly to AChE. Localization of junctional AChE on frozen sections of muscle with fluorescent Fasciculin-2 shows that the labeled toxin dissociates with a half-life of about 36h. The fluorescent toxin can subsequently be taken up by the muscle fibers by endocytosis giving the appearance of enzyme recycling. Newly synthesized AChE molecules undergo a lengthy series of processing events before final transport to the cell surface and association with the synaptic basal lamina. Following co-translational glycosylation the catalytic subunit polypeptide chain interacts with several molecular chaperones, glycosidases and glycosyltransferases to produce a catalytically active enzyme that can subsequently bind to one of two non-catalytic subunits. These molecular chaperones can be rate limiting steps in the assembly process. Treatment of muscle cells with a synthetic peptide containing the PRAD attachment sequence and a KDEL retention signal results in a large increase in assembled and exportable AChE, providing an additional level of post-translational control. Finally, we have found that Pumilio2, a member of the PUF family of RNA-binding proteins, is highly concentrated at the vertebrate neuromuscular junction where it plays an important role in regulating AChE translation through binding to a highly conserved NANOS response element in the 3'-UTR. Together, these studies define several new levels of AChE regulation in electrically excitable cells. 相似文献
962.
Sannella AR Casini A Gabbiani C Messori L Bilia AR Vincieri FF Majori G Severini C 《FEBS letters》2008,582(6):844-847
The clinically established gold-based antiarthritic drug auranofin (AF) manifests a pronounced reactivity toward thiol and selenol groups of proteins. In particular, AF behaves as a potent inhibitor of mammalian thioredoxin reductases causing severe intracellular oxidative stress. Given the high sensitivity of Plasmodium falciparum to oxidative stress, we thought that auranofin might act as an effective antimalarial agent. Thus, we report here new experimental results showing that auranofin and a few related gold complexes strongly inhibit P. falciparum growth in vitro. The observed antiplasmodial effects probably arise from direct inhibition of P. falciparum thioredoxin reductase. The above findings and the safe toxicity profile of auranofin warrant rapid evaluation of AF for malaria treatment in animal models. 相似文献
963.
Although fungi do not cause outbreaks or pandemics, the incidence of severe systemic fungal infections has increased significantly, mainly because of the explosive growth in the number of patients with compromised immune system. Thus, drug resistance in pathogenic fungi, including dermatophytes, is gaining importance. The molecular aspects involved in the resistance of dermatophytes to marketed antifungals and other cytotoxic drugs, such as modifications of target enzymes, over-expression of genes encoding ATP-binding cassette (ABC) transporters and stress-response-related proteins are reviewed. Emphasis is placed on the mechanisms used by dermatophytes to overcome the inhibitory action of terbinafine and survival in the host environment. The relevance of identifying new molecular targets, of expanding the understanding about the molecular mechanisms of resistance and of using this information to design new drugs or to modify those that have become ineffective is also discussed. 相似文献
964.
Here we summarized what is known at the present about function, structure and effect of mutations in the human prolidase.
Among the peptidases, prolidase is the only metalloenzyme that cleaves the iminodipeptides containing a proline or hydroxyproline
residue at the C-terminal end. It is relevant in the latest stage of protein catabolism, particularly of those molecules rich
in imino acids such as collagens, thus being involved in matrix remodelling. Beside its intracellular functions, prolidase
has an antitoxic effect against some organophosphorus molecules, can be used in dietary industry as bitterness reducing agent
and recently has been used as target enzyme for specific melanoma prodrug activation. Recombinant human prolidase was produced
in prokaryotic and eukaryotic hosts with biochemical properties similar to the endogenous enzyme and represents a valid tool
both to better understand the structure and biological function of the enzyme and to develop an enzyme replacement therapy
for the prolidase deficiency (PD). Prolidase deficiency is a rare recessive disorder caused by mutations in the prolidase
gene and characterized by severe skin lesions. Single amino acid substitutions, exon splicing, deletions and a duplication
were described as causative for the disease and are mainly located at highly conserved amino acids in the sequence of prolidase
from different species. The pathophysiology of PD is still poorly understood; we offer here a review of the molecular mechanisms
so far hypothesized. 相似文献
965.
Robert W. Evans Roozina Rafique Adel Zarea Chiara Rapisarda Richard Cammack Patricia J. Evans John B. Porter Robert C. Hider 《Journal of biological inorganic chemistry》2008,13(1):57-74
Despite its importance in iron-overload diseases, little is known about the composition of plasma non-transferrin-bound iron
(NTBI). Using 30-kDa ultrafiltration, plasma from thalassemic patients consisted of both filterable and non-filterable NTBI,
the filterable fraction representing less than 10% NTBI. Low filterability could result from protein binding or NTBI species
exceeding 30 kDa. The properties of iron citrate and its interaction with albumin were therefore investigated, as these represent
likely NTBI species. Iron permeated 5- or 12-kDa ultrafiltration units completely when complexes were freshly prepared and
citrate exceeded iron by tenfold, whereas with 30-kDa ultrafiltration units, permeation approached 100% at all molar ratios.
A g = 4.3 electron paramagnetic resonance signal, characteristic of mononuclear iron, was detectable only with iron-to-citrate
ratios above 1:100. The ability of both desferrioxamine and 1,2-dimethyl-3-hydroxypyridin-4-one to chelate iron in iron citrate
complexes also increased with increasing ratios of citrate to iron. Incremental molar excesses of citrate thus favour the
progressive appearance of chelatable lower molecular weight iron oligomers, dimers and ultimately monomers. Filtration of
iron citrate in the presence of albumin showed substantial binding to albumin across a wide range of iron-to-citrate ratios
and also increased accessibility of iron to chelators, reflecting a shift towards smaller oligomeric species. However, in
vitro experiments using immunodepletion or absorption of albumin to Cibacron blue–Sepharose indicate that iron is only loosely
bound in iron citrate–albumin complexes and that NTBI is unlikely to be albumin-bound to any significant extent in thalassemic
sera. 相似文献
966.
967.
Soifer HS Sano M Sakurai K Chomchan P Saetrom P Sherman MA Collingwood MA Behlke MA Rossi JJ 《Nucleic acids research》2008,36(20):6511-6522
In humans a single species of the RNAseIII enzyme Dicer processes both microRNA precursors into miRNAs and long double-stranded RNAs into small interfering RNAs (siRNAs). An interesting but poorly understood domain of the mammalian Dicer protein is the N-terminal helicase-like domain that possesses a signature DExH motif. Cummins et al. created a human Dicer mutant cell line by inserting an AAV targeting cassette into the helicase domain of both Dicer alleles in HCT116 cells generating an in-frame 43-amino-acid insertion immediately adjacent to the DExH box. This insertion creates a Dicer mutant protein with defects in the processing of most, but not all, endogenous pre-miRNAs into mature miRNA. Using both biochemical and computational approaches, we provide evidence that the Dicer helicase mutant is sensitive to the thermodynamic properties of the stems in microRNAs and short-hairpin RNAs, with thermodynamically unstable stems resulting in poor processing and a reduction in the levels of functional mi/siRNAs. Paradoxically, this mutant exhibits enhanced processing efficiency and concomitant RNA interference when thermodynamically stable, long-hairpin RNAs are used. These results suggest an important function for the Dicer helicase domain in the processing of thermodynamically unstable hairpin structures. 相似文献
968.
Dissection of reverse gyrase activities: insight into the evolution of a thermostable molecular machine 总被引:2,自引:1,他引:1
Valenti A Perugino G D'Amaro A Cacace A Napoli A Rossi M Ciaramella M 《Nucleic acids research》2008,36(14):4587-4597
Reverse gyrase is a peculiar DNA topoisomerase, specific of thermophilic microorganisms, which induces positive supercoiling into DNA molecules in an ATP-dependent reaction. It is a modular enzyme and comprises an N-terminal helicase-like module fused to a C-terminal topoisomerase IA-like domain. The exact molecular mechanism of this unique reaction is not understood, and a fundamental mechanistic question is how its distinct steps are coordinated. We studied the cross-talk between the components of this molecular motor and probed communication between the DNA-binding sites and the different activities (DNA relaxation, ATP hydrolysis and positive supercoiling). We show that the isolated ATPase and topoisomerase domains of reverse gyrase form specific physical interactions, retain their own DNA binding and enzymatic activities, and when combined cooperate to achieve the unique ATP-dependent positive supercoiling activity. Our results indicate a mutual effect of both domains on all individual steps of the reaction. The C-terminal domain shows ATP-independent topoisomerase activity, which is repressed by the N-terminal domain in the full-length enzyme; experiments with the isolated domains showed that the C-terminal domain has stimulatory influence on the ATPase activity of the N-terminal domain. In addition, the two domains showed a striking reciprocal thermostabilization effect. 相似文献
969.
970.
Ambra Quacchia Chiara Ferracini Simona Bonelli Emilio Balletto Alberto Alma 《Biodiversity and Conservation》2008,17(6):1429-1437
Cacyreus marshalli Butler is an invasive species in many parts of Europe and Mediterranean area. In Europe, its larvae normally feed on pelargoniums.
We investigated its potential to spread to native Geranium spp. and evaluated the conservation risks that such a shift would pose for both native geraniums and cohabitant butterflies.
The host plant preferences of the Geranium Bronze were investigated under controlled conditions. Studies included both no-choice
and multi-choice tests, respectively using 9 and 6 Italian native Geranium spp. Host plant preferences were evaluated by counting the number of eggs laid on individual plants and following butterfly
development until adult emergence. Under no-choice conditions, at least one egg was recorded on each tested plant, except
for G. phaeum L. All the plants on which oviposition occurred were fully suitable for larval development. The butterfly, however, clearly
preferred three species, i.e. G. pratense L., G. sanguineum L. and G. sylvaticum L. for oviposition. In multi-choice trials, females laid at least one egg on all the tested plants, with a preference for
G. pratense and G. sylvaticum. In presence of Pelargonium spp. plants, however, no oviposition was observed on any Geranium spp. We assessed offspring fitness measuring their wingspan. No statistical differences were detected in the wingspan between
adults emerged from Geranium and Pelargonium. Cacyreus marshalli represents a potential threat for both native geraniums and for Geranium-consuming lycaenids, such as Aricia nicias Meigen and Eumedonia eumedon Esper. 相似文献