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101.
Structure of Trichamide, a Cyclic Peptide from the Bloom-Forming Cyanobacterium Trichodesmium erythraeum, Predicted from the Genome Sequence 下载免费PDF全文
Sebastian Sudek Margo G. Haygood Diaa T. A. Youssef Eric W. Schmidt 《Applied microbiology》2006,72(6):4382-4387
A gene cluster for the biosynthesis of a new small cyclic peptide, dubbed trichamide, was discovered in the genome of the global, bloom-forming marine cyanobacterium Trichodesmium erythraeum ISM101 because of striking similarities to the previously characterized patellamide biosynthesis cluster. The tri cluster consists of a precursor peptide gene containing the amino acid sequence for mature trichamide, a putative heterocyclization gene, an oxidase, two proteases, and hypothetical genes. Based upon detailed sequence analysis, a structure was predicted for trichamide and confirmed by Fourier transform mass spectrometry. Trichamide consists of 11 amino acids, including two cysteine-derived thiazole groups, and is cyclized by an N—C terminal amide bond. As the first natural product reported from T. erythraeum, trichamide shows the power of genome mining in the prediction and discovery of new natural products. 相似文献
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Hassan HM Sallam AA Mohammed R Hifnawy MS Youssef DT El Sayed KA 《Bioorganic & medicinal chemistry》2011,19(16):4928-4934
Sarcophine (1) is a bioactive cembranoid diterpene isolated from the Red Sea soft coral Sarcophyton glaucum. Previous semisynthesis attempts resulted in decreased or complete loss of 1's anticancer activity. Sarcophine and analogues showed antimigratory activity against breast and prostate cancer cell lines. This encouraged further semisynthestic optimizations to improve its activity and establish a preliminary structure-activity relationship. Eight new and five known semisynthetic analogues were generated. These compounds were evaluated for their ability to inhibit growth, proliferation, and migration of the prostate and breast metastatic cancer cell lines PC-3 and MDA-MB-231, respectively. Most analogues exhibited enhanced antimigratory activity. 相似文献
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Wichmann HE Kuhn KA Waldenberger M Schmelcher D Schuffenhauer S Meitinger T Wurst SH Lamla G Fortier I Burton PR Peltonen L Perola M Metspalu A Riegman P Landegren U Taussig MJ Litton JE Fransson MN Eder J Cambon-Thomsen A Bovenberg J Dagher G van Ommen GJ Griffith M Yuille M Zatloukal K 《Nature biotechnology》2011,29(9):795-797
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Dagher PC Mai EM Hato T Lee SY Anderson MD Karozos SC Mang HE Knipe NL Plotkin Z Sutton TA 《American journal of physiology. Renal physiology》2012,302(2):F284-F291
Inhibition of the tumor suppressor p53 diminishes tubular cell apoptosis and protects renal function in animal models of acute kidney injury (AKI). Therefore, targeting p53 has become an attractive therapeutic strategy in the approach to AKI. Although the acute protective effects of p53 inhibition in AKI have been examined, there is still relatively little known regarding the impact of acute p53 inhibition on the chronic sequelae of AKI. Consequently, we utilized the p53 inhibitor pifithrin-α to examine the long-term effects of p53 inhibition in a rodent model of ischemic AKI. Male Sprague-Dawley rats were subjected to bilateral renal artery clamping for 30 min followed by reperfusion for up to 8 wk. Pifithrin-α or vehicle control was administered at the time of surgery and then daily for 2 days [brief acute administration (BA)] or 7 days [prolonged acute administration (PA)]. Despite the acute protective effect of pifithrin-α in models of ischemic AKI, we found no protection in the microvascular rarefaction at 4 wk or development fibrosis at 8 wk with pifithrin-α administered on the BA schedule compared with vehicle control-treated animals. Furthermore, pifithrin-α administered on a PA schedule actually produced worse fibrosis compared with vehicle control animals after ischemic injury [21%/area (SD4.4) vs.16%/area (SD3.6)] as well as under sham conditions [2.6%/area (SD1.8) vs. 4.7%/area (SD1.3)]. The development of fibrosis with PA administration was independent of microvascular rarefaction. We identified enhanced extracellular matrix production, epithelial-to-mesenchymal transition, and amplified inflammatory responses as potential contributors to the augmented fibrosis observed with PA administration of pifithrin-α. 相似文献
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Tondu AL Robichon C Yvan-Charvet L Donne N Le Liepvre X Hajduch E Ferré P Dugail I Dagher G 《The Journal of biological chemistry》2005,280(39):33536-33540
Scavenger receptor class B, type I (SR-BI) mediates the selective uptake of lipids from high density lipoproteins and is expressed in several types of tissues. However, to date little is known about its role in adipocytes. In this study, we investigated the cellular distribution of SR-BI in 3T3-L1 adipocytes and its regulation by hormones known to increase lipid storage such as angiotensin II (Ang II) and insulin. SR-BI was mainly distributed in the cytoplasm as determined by laser-scanning confocal analysis of the immunofluorescence labeling of SR-BI or the study of an enhanced green fluorescent protein-tagged SR-BI fusion protein. Exposure of cells to either insulin or Ang II (1-2 h) induced the mobilization of SR-BI from intracellular pools to the plasma membrane. This was further confirmed by Western blotting on purified plasma membrane and by fluorescence-activated cell sorter analysis of the SR-BI receptor. Similar results were also observed in primary adipocytes. We also demonstrated that, in the presence of either insulin or Ang II, SR-BI translocation to the cell membrane is functional, because insulin and Ang II induced a significant increase in the high density lipoprotein-delivered 22-(N-7-nitrobenz-2-oxa-1,3-diazo-4-yl)-amino-23,24-bisnor-5-cholen-3-ol uptake and in total cholesterol content. These data demonstrate that SR-BI can be acutely mobilized from intracellular stores to the cell surface by insulin or Ang II, two hormones that exert lipogenic effects in adipocytes. This suggests that SR-BI might participate in the storage of lipids in the adipose tissue. 相似文献
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Batiuk Thomas D.; Schnizlein-Bick Carol; Plotkin Zoya; Dagher Pierre C. 《American journal of physiology. Cell physiology》2001,281(6):C1776
Guanine nucleosides aretoxic to some forms of cancer. This toxicity is pronounced in cancerswith upregulated guanine nucleotide synthesis, but the mechanisms arepoorly understood. We investigated this toxicity by measuring theeffects of guanine nucleosides on nucleotides in Jurkat cells usingHPLC. We also measured proliferation and cell death with microscopy andfluorescence-activated cell sorting. Guanosine increased GTP to 600%and reduced ATP to 40% of control. This resulted in cell death with apredominance of necrosis. Deoxyguanosine caused similar increases inGTP but at earlier time points. Cell death was severe with apredominance of apoptosis. Deoxyguanosine but not guanosineincreased dGTP to 800% of control. Adenosine inhibited the effects ofguanosine, in part by competing for uptake. In stimulated leukocytes,guanosine and deoxyguanosine altered the nucleotide pools in a wayqualitatively similar to that observed in Jurkat cells. However,proliferation was enhanced rather than impaired. In conclusion,guanosine and deoxyguanosine are toxic to Jurkat cells through twomechanisms: ATP depletion, causing necrosis, and the accumulation ofdGTP, resulting in apoptosis. 相似文献
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