Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Girish Rajendraprasad"'
Autor:
Susana Eibes, Girish Rajendraprasad, Claudia Guasch-Boldu, Mirela Kubat, Yulia Steblyanko, Marin Barisic
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Accurate chromosome segregation in mitosis depends on multiprotein structures called kinetochores that are built on the centromeric region of sister chromatids and serve to capture mitotic spindle microtubules. In early mitosis, unattached k
Externí odkaz:
https://doaj.org/article/1daa5f4d16d84a39970aa15a6bcdca50
Autor:
Kirstine Lavrsen, Girish Rajendraprasad, Marcin Leda, Susana Eibes, Elisa Vitiello, Vasileios Katopodis, Andrew B. Goryachev, Marin Barisic
Publikováno v:
Lavrsen, K, Rajendraprasad, G, Leda, M, Eibes, S, Vitiello, E, Katopodis, V, Goryachev, A B & Barisic, M 2023, ' Microtubule detyrosination drives symmetry breaking to polarize cells for directed cell migration ', Proceedings of the National Academy of Sciences, vol. 120, no. 22, e2300322120 . https://doi.org/10.1073/pnas.2300322120
To initiate directed movement, cells must become polarized, establishing a protrusive leading edge and a contractile trailing edge. This symmetry-breaking process involves reorganization of cytoskeleton and asymmetric distribution of regulatory molec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4779f9bf9eaf0c087bbbeb95ccf063b
https://www.pure.ed.ac.uk/ws/files/348350550/pnas.2300322120.pdf
https://www.pure.ed.ac.uk/ws/files/348350550/pnas.2300322120.pdf
Autor:
Gianmatteo Vit, Joana Duro, Girish Rajendraprasad, Emil P T Hertz, Lya Katrine Kauffeldt Holland, Melanie Bianca Weisser, Brennan C McEwan, Blanca Lopez‐Mendez, Paula Sotelo‐Parrilla, A Arockia Jeyaprakash, Guillermo Montoya, Niels Mailand, Kenji Maeda, Arminja Kettenbach, Marin Barisic, Jakob Nilsson
Publikováno v:
Vit, G, Duro, J, Rajendraprasad, G, Hertz, E P T, Holland, L K K, Weisser, M B, McEwan, B C, Lopez-Mendez, B, Sotelo-Parrilla, P, Jeyaprakash, A A, Montoya, G, Mailand, N, Maeda, K, Kettenbach, A, Barisic, M & Nilsson, J 2022, ' Chemogenetic profiling reveals PP2A-independent cytotoxicity of proposed PP2A activators iHAP1 and DT-061 ', EMBO Journal, vol. 41, no. 14, e110611 . https://doi.org/10.15252/embj.2022110611
Protein phosphatase 2A (PP2A) is an abundant phosphoprotein phosphatase that acts as a tumor suppressor. For this reason, compounds able to activate PP2A are attractive anticancer agents. The compounds iHAP1 and DT-061 have recently been reported to
Autor:
Kirstine Lavrsen, Girish Rajendraprasad, Marcin Leda, Susana Eibes, Elisa Vitiello, Vasileios Katopodis, Andrew Goryachev, Marin Barisic
Publikováno v:
SSRN Electronic Journal.
Autor:
Brennan C McEwan, Marin Barisic, Gianmatteo Vit, Blanca López-Méndez, Kenji Maeda, Jakob Nilsson, Guillermo Montoya, Arminja N. Kettenbach, Lya Katrine Kauffeldt Holland, Niels Mailand, Emil Peter Thrane Hertz, Girish Rajendraprasad, Joana Duro, Melanie Bianca Weisser
PP2A is an abundant phosphoprotein phosphatase that acts as a tumor suppressor. For this reason, compounds able to activate PP2A are attractive anticancer agents. The small molecule compounds iHAP1 and DT-061 have recently been reported by Leonard et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::451c3956bfc6131e63300f7ccff8637b
https://doi.org/10.1101/2021.07.08.451586
https://doi.org/10.1101/2021.07.08.451586
Molecular basis of vasohibins-mediated detyrosination and its impact on spindle function and mitosis
Autor:
Girish Rajendraprasad, Gao Wu, Shanhui Liao, Marin Barisic, Chao Xu, Jun Gao, Hongda Huang, Na Wang, Susana Eibes, Xiaoming Tu, Huijuan Yu
Publikováno v:
Cell Res
α-Tubulin detyrosination, largely catalyzed by vasohibins, is involved in many microtubule (MT)-related cellular events. In this study, we identified a core heterodimeric complex of human small vasohibin-binding protein (SVBP) and vasohibin 1 (VASH1
Autor:
Marin Barisic, Girish Rajendraprasad
Publikováno v:
BioEssays : news and reviews in molecular, cellular and developmental biologyREFERENCES. 43(8)
Continuous poleward motion of microtubules in metazoan mitotic spindles has been fascinating generations of cell biologists over the last several decades. In human cells, this so-called poleward flux was recently shown to be driven by the coordinated
Publikováno v:
Seminars in celldevelopmental biology. 117
The mitotic spindle is a bipolar cellular structure, built from tubulin polymers, called microtubules, and interacting proteins. This macromolecular machine orchestrates chromosome segregation, thereby ensuring accurate distribution of genetic materi
Publikováno v:
Rajendraprasad, G, Eibes, S, Boldú, C G & Barisic, M 2021, ' TH588 and low-dose nocodazole impair chromosome congression by suppressing microtubule turnover within the mitotic spindle ', Cancers, vol. 13, no. 23, 5995 . https://doi.org/10.3390/cancers13235995
Cancers
Cancers; Volume 13; Issue 23; Pages: 5995
Cancers, Vol 13, Iss 5995, p 5995 (2021)
Cancers
Cancers; Volume 13; Issue 23; Pages: 5995
Cancers, Vol 13, Iss 5995, p 5995 (2021)
Simple Summary A promising anti-cancer compound TH588 has been recently identified as a microtubule-targeting agent that inhibits tubulin polymerization in vitro and interferes with microtubule dynamics in interphase cells. Although it was shown to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fbf4e32134400b6b09190eaf423a3ff
https://curis.ku.dk/portal/da/publications/th588-and-lowdose-nocodazole-impair-chromosome-congression-by-suppressing-microtubule-turnover-within-the-mitotic-spindle(5b4e3015-1347-489f-89b0-c92991da0499).html
https://curis.ku.dk/portal/da/publications/th588-and-lowdose-nocodazole-impair-chromosome-congression-by-suppressing-microtubule-turnover-within-the-mitotic-spindle(5b4e3015-1347-489f-89b0-c92991da0499).html
Autor:
Ariana Jacome, Stephan Geley, Yulia Steblyanko, Girish Rajendraprasad, Helder Maiato, Marin Barisic, António J. Pereira, Mariana Osswald, Susana Eibes
Publikováno v:
EMBO J
Mitotic spindle microtubules (MTs) undergo continuous poleward flux, whose driving force and function in humans remain unclear. Here, we combined loss‐of‐function screenings with analysis of MT‐dynamics in human cells to investigate the molecul