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131.
Tariq MA Soedipe A Ramesh G Wu H Zhang Y Shishodia S Gridley DS Pourmand N Jejelowo O 《Molecular and cellular biochemistry》2011,349(1-2):213-218
The space radiation environment consists of trapped particle radiation, solar particle radiation, and galactic cosmic radiation (GCR), in which protons are the most abundant particle type. During missions to the moon or to Mars, the constant exposure to GCR and occasional exposure to particles emitted from solar particle events (SPE) are major health concerns for astronauts. Therefore, in order to determine health risks during space missions, an understanding of cellular responses to proton exposure is of primary importance. The expression of DNA repair genes in response to ionizing radiation (X-rays and gamma rays) has been studied, but data on DNA repair in response to protons is lacking. Using qPCR analysis, we investigated changes in gene expression induced by positively charged particles (protons) in four categories (0, 0.1, 1.0, and 2.0 Gy) in nine different DNA repair genes isolated from the testes of irradiated mice. DNA repair genes were selected on the basis of their known functions. These genes include ERCC1 (5' incision subunit, DNA strand break repair), ERCC2/NER (opening DNA around the damage, Nucleotide Excision Repair), XRCC1 (5' incision subunit, DNA strand break repair), XRCC3 (DNA break and cross-link repair), XPA (binds damaged DNA in preincision complex), XPC (damage recognition), ATA or ATM (activates checkpoint signaling upon double strand breaks), MLH1 (post-replicative DNA mismatch repair), and PARP1 (base excision repair). Our results demonstrate that ERCC1, PARP1, and XPA genes showed no change at 0.1 Gy radiation, up-regulation at 1.0 Gy radiation (1.09 fold, 7.32 fold, 0.75 fold, respectively), and a remarkable increase in gene expression at 2.0 Gy radiation (4.83 fold, 57.58 fold and 87.58 fold, respectively). Expression of other genes, including ATM and XRCC3, was unchanged at 0.1 and 1.0 Gy radiation but showed up-regulation at 2.0 Gy radiation (2.64 fold and 2.86 fold, respectively). We were unable to detect gene expression for the remaining four genes (XPC, ERCC2, XRCC1, and MLH1) in either the experimental or control animals. 相似文献
132.
133.
Rehman Hamza Akram Muzamal Kiyani Mubin Mustafa Yaseen Talha Ghani Abdul Saggu Javed Iqbal Shah Syed Sajid Hussain Khalid Zafar Mahmood Bokhari Syed Ali Imran 《Biological trace element research》2020,193(2):524-535
Biological Trace Element Research - Endoxylanase enzyme is used as poultry feed additive to degrade anti-nutritional factors like non-starch polysaccharides. Moreover, iron is one of the most... 相似文献
134.
Sami Ullah Farooq Anwar Muhammad Fayyaz ur Rehman Rahman Qadir Muhammad Safwan Akram 《化学与生物多样性》2023,20(7):e202300107
This article presents an optimized ultrasound-assisted ethanolic extraction (UAEE) and characterization of selected high-value components from Gemlik olive fruit (GOF) harvested from Potohar region of Pakistan. Response surface methodology (RSM), involving central composite design (CCD), was applied to optimize the extraction variables i. e., temperature (25–65 °C), extraction time (15–45 min) and aqueous ethanol concentration (60–90 %) for optimal recovery of bioactives extract, total phenolic contents (TPC) and DPPH free radical scavengers. Under the optimized set of conditions such as 43 °C temperature, 32 min extraction time and 80 % aqueous ethanol, the best extract yield (218.82 mg/g), TPC (19.87 mg GAE/g) and DPPH scavenging activity (63.04 %) were recorded. A quadratic polynomial model was found to be reasonably fitted to the observed results for extract yield (p<0.0001 and R2=0.9941), TPC (p<0.0001 and R2=0.9891), and DPPH radical scavenging activity (p<0.0001 and R2=0.9692). Potent phenolic compounds were identified by GC/MS in GOF extract and considerable amount of essential fatty acids were also detected. The current findings support the use of UAEE as an effective green route for optimized recovery of high-value components from GOF and hence its applications can be extended to functional food and nutra-pharmaceutical developments. 相似文献
135.
Wu S Avila-Sakar A Kim J Booth DS Greenberg CH Rossi A Liao M Li X Alian A Griner SL Juge N Yu Y Mergel CM Chaparro-Riggers J Strop P Tampé R Edwards RH Stroud RM Craik CS Cheng Y 《Structure (London, England : 1993)》2012,20(4):582-592
In spite of its recent achievements, the technique of single particle electron cryomicroscopy (cryoEM) has not been widely used to study proteins smaller than 100 kDa, although it is a highly desirable application of this technique. One fundamental limitation is that images of small proteins embedded in vitreous ice do not contain adequate features for accurate image alignment. We describe a general strategy to overcome this limitation by selecting a fragment antigen binding (Fab) to form a stable and rigid complex with a target protein, thus providing a defined feature for accurate image alignment. Using this approach, we determined a three-dimensional structure of an ~65 kDa protein by single particle cryoEM. Because Fabs can be readily generated against a wide range of proteins by phage display, this approach is generally applicable to study many small proteins by single particle cryoEM. 相似文献
136.
Barbara C. Figueiredo Natan R. G. Assis Suellen B. Morais Natasha D. Ricci Carina S. Pinheiro Vicente P. Martins Rodrigo M. Bicalho Akram A. Da'dara Patrick J. Skelly Sergio C. Oliveira 《PLoS neglected tropical diseases》2014,8(8)
Background
Schistosomiasis is a neglected tropical disease caused by several species of trematode of the genus Schistosoma. The disease affects more than 200 million people in the world and causes up to 280,000 deaths per year, besides having high morbidity due to chronic illness that damages internal organs. Current schistosomiasis control strategies are mainly based on chemotherapy, but many researchers believe that the best long-term strategy to control disease is a combination of drug treatment and immunization with an anti-schistosome vaccine. Among the most promising molecules as vaccine candidates are the proteins present in the tegument and digestive tract of the parasite.Methodology/Principal Findings
In this study, we describe for the first time Schistosoma mansoni syntenin (SmSynt) and we evaluate its potential as a recombinant vaccine. We demonstrate by real-time PCR that syntenin is mainly expressed in intravascular life stages (schistosomula and adult worms) of the parasite life cycle and, by confocal microscopy, we localize it in digestive epithelia in adult worms and schistosomula. Administration of siRNAs targeting SmSynt leads to the knock-down of syntenin gene and protein levels, but this has no demonstrable impact on parasite morphology or viability, suggesting that high SmSynt gene expression is not essential for the parasites in vitro. Mice immunization with rSmSynt, formulated with Freund''s adjuvant, induces a Th1-type response, as suggested by the production of IFN-γ and TNF-α by rSmSynt-stimulated cultured splenocytes. The protective effect conferred by vaccination with rSmSynt was demonstrated by 30–37% reduction of worm burden, 38–43% reduction in the number, and 35–37% reduction in the area, of liver granulomas.Conclusions/Significance
Our report is the first characterization of syntenin in Schistosoma mansoni and our data suggest that this protein is a potential candidate for the development of a multi-antigen vaccine to control schistosomiasis. 相似文献137.
Mahmoud S. El-Tarabany Akram A. El-Tarabany Mostafa A. Atta 《Biological Rhythm Research》2019,50(2):245-254
Understanding the seasonal patterns of estrus cycle in caprine is crucial to develop the efficient breeding plans in the subtropics. Thus, the aim of the current research was to evaluate the effects of breeding season on hormonal profile and blood biochemical indices at different stages of estrus cycle in normal breeding or out-of-season breeding in goats. Forty-four Baladi goats were monitored for a period of eight months (July–February). Baladi goats exhibit a normal seasonal breeding (NS) at midsummer and continue through the autumn season (68%), with a considerable percentage of females having estrus signs during out-of-season (OS) period (32%). At the mid and late luteal phases of estrus cycles, the NS breeding group had significantly higher serum progesterone level than that reported in the OS group (p = 0.013 and 0.039, respectively). At the estrus and late luteal phases of estrus cycles, the NS breeding group had significantly higher serum β-estradiol level than that reported in the OS group (p = 0.022 and 0.001, respectively). Compared to the OS group, the NS breeding group had significantly higher serum cholesterol at the mid and late luteal phases of estrus cycle (p = 0.001 and 0.016, respectively), and higher serum glucose level in the early luteal phase of the cycle (p = 0.009). In conclusion, the NS breeding goats had superior progesterone (mid-luteal and late luteal phases) and estradiol (estrus and late luteal phases) profiles than that reported in the OS group. This may indicate specific approaches to maintain the breeding efficiency of goats during the out-of-season period. 相似文献
138.
Akram M. El‐Didamony 《Luminescence》2011,26(2):112-117
Yttrium‐sensitized fluorescence was used to develop a sensitive and simple spectrofluorimetric method for the determination of sparfloxacin. The method is based on the strong fluorescence of sparfloxacin after adding the fluorescence probe yttrium in buffer solution (pH = 8), and various factors influencing fluorescence were investigated. Under optimum conditions, the enhanced fluorescence intensity of the system showed a good linear relationship with the concentration of sparfloxacin over the range 8 × 10?7 to 1.4 × 10?5 mol L?1 with a correlation coefficient of 0.9997. The detection limit (S/N = 3) was determined as 9.01 × 10?8 mol L?1. The mechanism of the sensitizing effect of probe was discussed. This method has been successfully applied for the determination of sparfloxacin in pharmaceuticals, human urine and serum samples; the result obtained was satisfactory. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
139.
Ilanchezhian Shanmugam Mohammad Abbas Farhan Ayoub Susan Mirabal Manal Bsaili Erin K. Caulder David M. Weinstock Alan E. Tomkinson Robert Hromas Monte Shaheen 《The Journal of biological chemistry》2014,289(33):22739-22748
Rad17 is a subunit of the Rad9-Hus1-Rad1 clamp loader complex, which is required for Chk1 activation after DNA damage. Rad17 has been shown to be regulated by the ubiquitin-proteasome system. We have identified a deubiquitylase, USP20 that is required for Rad17 protein stability in the steady-state and post DNA damage. We demonstrate that USP20 and Rad17 interact, and that this interaction is enhanced by UV exposure. We show that USP20 regulation of Rad17 is at the protein level in a proteasome-dependent manner. USP20 depletion results in poor activation of Chk1 protein by phosphorylation, consistent with Rad17 role in ATR-mediated phosphorylation of Chk1. Similar to other DNA repair proteins, USP20 is phosphorylated post DNA damage, and its depletion sensitizes cancer cells to damaging agents that form blocks ahead of the replication forks. Similar to Chk1 and Rad17, which enhance recombinational repair of collapsed replication forks, we demonstrate that USP20 depletion impairs DNA double strand break repair by homologous recombination. Together, our data establish a new function of USP20 in genome maintenance and DNA repair. 相似文献
140.