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Wyszukujesz frazę "Lenart, Agnieszka" wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Protein production and secretion in an Aspergillus nidulans mutant impaired in glycosylation.
Autorzy:
Perlińska-Lenart, Urszula
Kurzątkowski, Wiesław
Janas, Piotr
Kopińska, Agnieszka
Palamarczyk, Grażyna
Kruszewska, Joanna
Powiązania:
https://bibliotekanauki.pl/articles/1041477.pdf
Data publikacji:
2005
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
glycosylation
protein secretion
DPM1 gene
Aspergillus
dolichylphosphate mannose synthase
Opis:
O-glycosylation has been considered a limiting factor in protein secretion in filamentous fungi. Overexpression of the yeast DPM1 gene encoding dolichylphosphate mannose synthase (DPMS) in an Aspergillus nidulans mutant (BWB26A) deficient in O-glycosylation caused an increase in the number of secretory vesicles and changes in protein secretion. However, the secretory proteins, primarily O-mannosylated glucoamylase and N-glycosylated invertase, were mainly trapped in the periplasmic space. Different glycoforms of invertase were found insite the cells, in the periplasmic space and in the cultivation medium. Our data point to the importance of the cell wall as a barrier in protein secretion.
Źródło:
Acta Biochimica Polonica; 2005, 52, 1; 195-205
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Optimization of a retroviral vector for transduction of human CD34 positive cells
Autorzy:
Szyda, Anna
Paprocka, Maria
Krawczenko, Agnieszka
Lenart, Katarzyna
Heimrath, Jerzy
Grabarczyk, Piotr
Mackiewicz, Andrzej
Duś, Danuta
Powiązania:
https://bibliotekanauki.pl/articles/1041181.pdf
Data publikacji:
2006
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
transduction optimization
retroviral vector
CD34+ cells
Opis:
Human stem and progenitor cells have recently become objects of intensive studies as an important target for gene therapy and regenerative medicine. Retroviral vectors are among the most effective tools for genetic modification of these cells. However, their transduction efficiency strongly depends on the choice of the ex vivo transduction system. The aim of this study was to elaborate a system for retroviral vector transduction of human CD34 positive cells isolated from cord blood. The retroviral vector pMINV EGFP was chosen for transduction of two human erythroblastoid cell lines: KG-1a (CD34 positive) and K562 (CD34 negative). For vector construction, three promoters and two retroviral vector packaging cell lines were used. To optimize the physicochemical conditions of the transduction process, different temperatures of supernatant harvesting, the influence of centrifugation and the presence of transduction enhancing agents were tested. The conditions elaborated with KG-1a cells were further applied for transduction of CD34 positive cells isolated from cord blood. The optimal efficiency of transduction of CD34 positive cells with pMINV EGFP retroviral vector (26% of EGFP positive cells), was obtained using infective vector with LTR retroviral promoter, produced by TE FLY GA MINV EGFP packaging cell line. The transduction was performed in the presence of serum, at 37°C, with co-centrifugation of cells with viral supernatants and the use of transduction enhancing agents. This study confirmed that for gene transfer into CD34 positive cells, the detailed optimization of each element of the transduction process is of great importance.
Źródło:
Acta Biochimica Polonica; 2006, 53, 4; 815-823
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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