Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Chandrika N. Deshpande"'
Autor:
Chandrika N. Deshpande, T. Alex Ruwe, Ali Shawki, Vicky Xin, Kyle R. Vieth, Erika V. Valore, Bo Qiao, Tomas Ganz, Elizabeta Nemeth, Bryan Mackenzie, Mika Jormakka
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Ferroportin (Fpn) is essential for mammalian iron homeostasis as it exports iron from cells into blood circulation, but the molecular mechanisms of Fpn-mediated iron transport remain obscure. Here the authors use biophysical approaches to reveal that
Externí odkaz:
https://doaj.org/article/61dff6b0396e40ccba89522883e761ae
Autor:
Bo Qiao, So Iwata, Chandrika N. Deshpande, Mika Jormakka, Norimichi Nomura, Elizabeta Nemeth, Josep Font, Bryan Mackenzie, Corbin R. Azucenas, Tomas Ganz, Vicky Xin
Publikováno v:
FEBS Open Bio
Here, Deshpande et al. describe the production and purification of mouse ferroportin (Fpn), the only known mammalian iron efflux protein, and selective loop deletion constructs with enhanced thermal stability. Transport activity and hepcidin responsi
Autor:
Arianna Di Fazio, W. Bret Church, Michelle Sui Wen Xiang, Xin Maggie Wang, Cecy R. Xi, Hui Emma Zhang, Charles G. Bailey, Geoffrey W. McCaughan, Chandrika N. Deshpande, Yiqian Chen, Naveed A. Nadvi, Mehdi Sharifi Tabar, Mark D. Gorrell
Publikováno v:
Protein expression and purification. 181
Fibroblast activation protein alpha (FAP) is a cell-surface expressed type II glycoprotein that has a unique proteolytic activity. FAP has active soluble forms that retain the extracellular portion but lack the transmembrane domain and cytoplasmic ta
Autor:
Visaahini Sureshan, Chandrika N Deshpande, Yan Boucher, Jeremy E Koenig, Midwest Center for Structural Genomics, H W Stokes, Stephen J Harrop, Paul M G Curmi, Bridget C Mabbutt
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e52934 (2013)
Mobile gene cassettes captured within integron arrays encompass a vast and diverse pool of genetic novelty. In most cases, functional annotation of gene cassettes directly recovered by cassette-PCR is obscured by their characteristically high sequenc
Externí odkaz:
https://doaj.org/article/6e634f80edff4835b698d3756086353e
Autor:
Ana Julia Vieira de Ribeiro, Cecy R. Xi, Ariel Isaacs, Christopher L. D. McMillan, Arianna Di Fazio, K. Patel, Michelle Sui Wen Xiang, Mark D. Gorrell, Geoffrey W. McCaughan, Chandrika N. Deshpande, W. Bret Church, Joel P. Mackay, Brenna Osborne, Naveed A. Nadvi, Hui Emma Zhang, Yiqian Chen, Xiaonan Trixie Wang, Jason Low
Publikováno v:
Molecules
Molecules, Vol 25, Iss 5392, p 5392 (2020)
Volume 25
Issue 22
Molecules, Vol 25, Iss 5392, p 5392 (2020)
Volume 25
Issue 22
Proteases catalyse irreversible posttranslational modifications that often alter a biological function of the substrate. The protease dipeptidyl peptidase 4 (DPP4) is a pharmacological target in type 2 diabetes therapy primarily because it inactivate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5967ba4b1c4b2fd7da292bf6872c7dff
https://doi.org/10.20944/preprints202009.0390.v2
https://doi.org/10.20944/preprints202009.0390.v2
Autor:
Vicky Xin, T Alex Ruwe, Bryan Mackenzie, Kyle R. Vieth, Bo Qiao, Ali Shawki, Mika Jormakka, Chandrika N. Deshpande, Tomas Ganz, Erika V. Valore, Elizabeta Nemeth
Publikováno v:
Nature communications, vol 9, iss 1
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Deshpande, CN; Ruwe, TA; Shawki, A; Xin, V; Vieth, KR; Valore, EV; et al.(2018). Calcium is an essential cofactor for metal efflux by the ferroportin transporter family. NATURE COMMUNICATIONS, 9. doi: 10.1038/s41467-018-05446-4. UCLA: Retrieved from: http://www.escholarship.org/uc/item/0wp7091s
Nature Communications
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Deshpande, CN; Ruwe, TA; Shawki, A; Xin, V; Vieth, KR; Valore, EV; et al.(2018). Calcium is an essential cofactor for metal efflux by the ferroportin transporter family. NATURE COMMUNICATIONS, 9. doi: 10.1038/s41467-018-05446-4. UCLA: Retrieved from: http://www.escholarship.org/uc/item/0wp7091s
Nature Communications
Ferroportin (Fpn)—the only known cellular iron exporter—transports dietary and recycled iron into the blood plasma, and transfers iron across the placenta. Despite its central role in iron metabolism, our molecular understanding of Fpn-mediated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::019374d32f398be01e118b12e65275cb
https://escholarship.org/uc/item/0wp7091s
https://escholarship.org/uc/item/0wp7091s
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 9, p e0184366 (2017)
PLoS ONE, Vol 12, Iss 9, p e0184366 (2017)
Hephaestin is a large membrane-anchored multicopper ferroxidase involved in mammalian iron metabolism. Newly absorbed dietary iron is exported across the enterocyte basolateral membrane by the ferrous iron transporter ferroportin, but hephaestin incr
Autor:
Megan J. Maher, Amy P. Guilfoyle, Josep Font, Mika Jormakka, Aaron P. McGrath, Chandrika N. Deshpande
Publikováno v:
Acta Crystallographica Section F Structural Biology and Crystallization Communications. 69:399-404
FeoB is a transmembrane protein involved in ferrous iron uptake in prokaryotic organisms. FeoB comprises a cytoplasmic soluble domain termed NFeoB and a C-terminal polytopic transmembrane domain. Recent structures of NFeoB have revealed two structura
Autor:
Koichi Ito, Chandrika N. Deshpande, Mika Jormakka, Osamu Nureki, Reiya Taniguchi, Josep Font, Ryuichiro Ishitani, Hideaki E. Kato, Miki Wada
Publikováno v:
Nature Communications
In vertebrates, the iron exporter ferroportin releases Fe2+ from cells into plasma, thereby maintaining iron homeostasis. The transport activity of ferroportin is suppressed by the peptide hormone hepcidin, which exhibits upregulated expression in ch
Publikováno v:
Bioscience Reports
Bioscience Reports, Vol 34, Iss 6, p e00158 (2014)
Bioscience Reports, Vol 34, Iss 6, p e00158 (2014)
GDP release from GTPases is usually extremely slow and is in general assisted by external factors, such as association with guanine exchange factors or membrane-embedded GPCRs (G protein-coupled receptors), which accelerate the release of GDP by seve