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991.
992.
Nicolás Gastón Brukman Sol Yanel Nuñez Lis del Carmen Puga Molina Mariano Gabriel Buffone Alberto Darszon Patricia Sara Cuasnicu Vanina Gabriela Da Ros 《Journal of cellular physiology》2019,234(4):5276-5288
Capacitation is a mandatory process for the acquisition of mammalian sperm fertilization competence and involves the activation of a complex and still not fully understood system of signaling pathways. Under in vitro conditions, there is an increase in both protein tyrosine phosphorylation (pTyr) and intracellular Ca2+ levels in several species. In human sperm, results from our group revealed that pTyr signaling can be blocked by inhibiting proline-rich tyrosine kinase 2 (PYK2). Based on the role of PYK2 in other cell types, we investigated whether the PYK2-dependent pTyr cascade serves as a sensor for Ca 2+ signaling during human sperm capacitation. Flow cytometry studies showed that exposure of sperm to the PYK2 inhibitor N-[2-[[[2-[(2,3-dihydro-2-oxo-1 H-indol-5-yl)amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]methyl]phenyl]- N-methyl-methanesulfonamide hydrate (PF431396) produced a significant and concentration-dependent reduction in intracellular Ca 2+ levels during capacitation. Further studies revealed that PF431396-treated sperm exhibited a decrease in the activity of CatSper, a key sperm Ca 2+ channel. In addition, time course studies during capacitation in the presence of PF431396 showed a significant and sustained decrease in both intracellular Ca 2+ and pH levels after 2 hr of incubation, temporarily coincident with the activation of PYK2 during capacitation. Interestingly, decreases in Ca 2+ levels and progressive motility caused by PF431396 were reverted by inducing intracellular alkalinization with NH 4Cl, without affecting the pTyr blockage. Altogether, these observations support pTyr as an intracellular sensor for Ca 2+ entry in human sperm through regulation of cytoplasmic pH. These results contribute to a better understanding of the modulation of the polymodal CatSper and signaling pathways involved in human sperm capacitation. 相似文献
993.
994.
Sarah M. Smith Kelly L. Walker Alexander S. Jones Corinne J. Smith Colin Robinson 《Biotechnology and bioengineering》2019,116(4):722-733
The large-scale production and isolation of recombinant protein is a central element of the biotechnology industry and many of the products have proved extremely beneficial for therapeutic medicine. Escherichia coli is the microorganism of choice for the expression of heterologous proteins for therapeutic application, and a range of high-value proteins have been targeted to the periplasm using the well characterized Sec protein export pathway. More recently, the ability of the second mainstream protein export system, the twin-arginine translocase, to transport fully-folded proteins into the periplasm of not only E. coli, but also other Gram-negative bacteria, has captured the interest of the biotechnology industry. In this study, we have used a novel approach to block the export of a heterologous Tat substrate in the later stages of the export process, and thereby generate a single-span membrane protein with the soluble domain positioned on the periplasmic side of the inner membrane. Biochemical and immuno-electron microscopy approaches were used to investigate the export of human growth hormone by the twin-arginine translocase, and the generation of a single-span membrane-embedded variant. This is the first time that a bonafide biotechnologically relevant protein has been exported by this machinery and visualized directly in this manner. The data presented here demonstrate a novel method for the production of single-span membrane proteins in E. coli. 相似文献
995.
Mayra Domínguez-Pérez Arturo Simoni-Nieves Patricia Rosales Natalia Nuño-Lámbarri Mónica Rosas-Lemus Verónica Souza Roxana U. Miranda Leticia Bucio Salvador Uribe Carvajal Jens U. Marquardt Daekwan Seo Luis E. Gomez-Quiroz María Concepción Gutiérrez-Ruiz 《Journal of cellular physiology》2019,234(5):7213-7223
996.
Patricia L. Sez Betsy K. Rivera Constanza F. Ramírez Valentina Vallejos Lohengrin A. Cavieres Luis J. Corcuera Len A. Bravo 《Physiologia plantarum》2019,165(3):511-523
Regional climate change in Antarctica would favor the carbon assimilation of Antarctic vascular plants, since rising temperatures are approaching their photosynthetic optimum (10–19°C). This could be detrimental for photoprotection mechanisms, mainly those associated with thermal dissipation, making plants more susceptible to eventual drought predicted by climate change models. With the purpose to study the effect of temperature and water availability on light energy utilization and putative adjustments in photoprotective mechanisms of Deschampsia antarctica Desv., plants were collected from two Antarctic provenances: King George Island and Lagotellerie Island. Plants were cultivated at 5, 10 and 16°C under well‐watered (WW) and water‐deficit (WD, at 35% of the field capacity) conditions. Chlorophyll fluorescence, pigment content and de‐epoxidation state were evaluated. Regardless of provenances, D. antarctica showed similar morphological, biochemical and functional responses to growth temperature. Higher temperature triggered an increase in photochemical activity (i.e. electron transport rate and photochemical quenching), and a decrease in thermal dissipation capacity (i.e. lower xanthophyll pool, Chl a/b and β carotene/neoxanthin ratios). Leaf mass per unit area was reduced at higher temperature, and was only affected in plants exposed to WD at 16°C and exhibiting lower electron transport rate and amount of chlorophylls. D. antarctica is adapted to frequent freezing events, which may induce a form of physiological water stress. Photoprotective responses observed under WD contribute to maintain a stable photochemical activity. Thus, it is possible that short‐term temperature increases could favor the photochemical activity of this species. However, long‐term effects will depend on the magnitude of changes and the plant's ability to adjust to new growth temperature. 相似文献
997.
Christine R. Beck Claudia M.B. Carvalho Zeynep C. Akdemir Fritz J. Sedlazeck Xiaofei Song Qingchang Meng Jianhong Hu Harsha Doddapaneni Zechen Chong Edward S. Chen Philip C. Thornton Pengfei Liu Bo Yuan Marjorie Withers Shalini N. Jhangiani Divya Kalra Kimberly Walker Adam C. English James R. Lupski 《Cell》2019,176(6):1310-1324.e10
998.
999.
Sakhanokho Hamidou F. Babiker Ebrahiem M. Smith Barbara J. Drackett Patricia R. 《Plant Cell, Tissue and Organ Culture》2019,137(3):637-637
Plant Cell, Tissue and Organ Culture (PCTOC) - There were two errors in the original publication: The copyright holder was specified as Springer Nature B.V. The correct information is as follows:... 相似文献
1000.