GroEL Apical Domain, DsbA and DsbC immobilized in cellulose assisted the chromatographic oxidative refolding of lysozyme

2010 ◽  
Vol 150 ◽  
pp. 85-86 ◽  
Author(s):  
A. Antonio-Perez ◽  
J. Ortega-Lopez
2012 ◽  
Vol 17 (4) ◽  
pp. 703-710 ◽  
Author(s):  
Aurora Antonio-Pérez ◽  
Tania Rivera-Hernández ◽  
Luz María Aldaz-Martínez ◽  
Jaime Ortega-López

2007 ◽  
Vol 282 (37) ◽  
pp. 27556
Author(s):  
Bing-Rui Zhou ◽  
Yi Liang ◽  
Fen Du ◽  
Zheng Zhou ◽  
Jie Chen

Author(s):  
Lakshmi Balasubramanian ◽  
Vanessa Zuzarte-Luís ◽  
Tabish Syed ◽  
Debakshi Mullick ◽  
Saptarathi Deb ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Li-Ting Wang ◽  
Abira Rajah ◽  
Claire M. Brown ◽  
Luke McCaffrey

AbstractPolarized epithelial cells can organize into complex structures with a characteristic central lumen. Lumen formation requires that cells coordinately orient their polarity axis so that the basolateral domain is on the outside and apical domain inside epithelial structures. Here we show that the transmembrane aminopeptidase, CD13, is a key determinant of epithelial polarity orientation. CD13 localizes to the apical membrane and associates with an apical complex with Par6. CD13-deficient cells display inverted polarity in which apical proteins are retained on the outer cell periphery and fail to accumulate at an intercellular apical initiation site. Here we show that CD13 is required to couple apical protein cargo to Rab11-endosomes and for capture of endosomes at the apical initiation site. This role in polarity utilizes the short intracellular domain but is independent of CD13 peptidase activity.


2017 ◽  
Vol 430 (2) ◽  
pp. 346-361 ◽  
Author(s):  
Aldine R. Amiel ◽  
Hereroa Johnston ◽  
Taylor Chock ◽  
Paul Dahlin ◽  
Marta Iglesias ◽  
...  

PLoS ONE ◽  
2010 ◽  
Vol 5 (3) ◽  
pp. e9480 ◽  
Author(s):  
Geng Chen ◽  
Garrett P. League ◽  
Sang-Chul Nam

1998 ◽  
Vol 123 (3) ◽  
pp. 516-520 ◽  
Author(s):  
I. Nishimura ◽  
M. Uchida ◽  
Y. Inohana ◽  
K. Setoh ◽  
K. Daba ◽  
...  
Keyword(s):  

2018 ◽  
Author(s):  
Weronika Fic ◽  
Celia Faria ◽  
Daniel St Johnston

AbstractThe timing of Drosophila egg chamber development is controlled by a germline Delta signal that activates Notch in the follicle cells to induce them to cease proliferation and differentiate. Here we report that follicle cells lacking the RNA-binding protein IMP go through one extra division due to a delay in the Delta-dependent S2 cleavage of Notch. The timing of Notch activation has previously been shown to be controlled by cis-inhibition by Delta in the follicle cells, which is relieved when the miRNA pathway represses Delta expression. imp mutants are epistatic to Delta mutants and give an additive phenotype with belle and dicer mutants, indicating that IMP functions independently of both cis-inhibition and the miRNA pathway. We find that the imp phenotype is rescued by over-expression of Kuzbanian, the metalloprotease that mediates the Notch S2 cleavage. Furthermore, Kuzbanian is not enriched at the apical membrane in imp mutants, accumulating instead in late endosomes. Thus, IMP regulates Notch signalling by controlling the localisation of Kuzbanian to the apical domain, where Notch cleavage occurs, revealing a novel regulatory step in the Notch pathway.SummaryIMP regulates Notch signalling in follicle cells by controlling Kuzbanian localisation to the apical domain, where Notch cleavage occurs, revealing a novel regulatory step in the Notch pathway.


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