Lubos Cipak

Dr. Lubos Cipak

Cancer Research Institute, Biomedical Research Center, Slovak Academy of Sciences, Slovak Republic
orcid

Research Focus & Metrics

Academic Career Length

57Years (1970-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2010 in Cell Cycle
Verified
Journal Article
Open access
CRCornelia Rumpf
Cornelia Rumpf
LCLubos Cipak
Lubos Cipak
ADAndrej Dudas
Andrej Dudas
ZBZsigmond Benko
Zsigmond Benko
MPMiroslava Požgajová
Miroslava Požgajová
Juraj GreganJuraj Gregan
Juraj Gregan
Segregation of chromosomes during meiosis depends on separase cleavage of Rec8, the meiosis-specific alpha-kleisin subunit of cohesin. We mapped Rec8 phosphorylation sites by mass spectrometry and ...

1 February 2007 in Toxicology in Vitro
Verified
Journal Article
Closed access
SJSona Jantova
Sona Jantova
LCLubos Cipak
Lubos Cipak
SLSilvia Letasiova
Silvia Letasiova

1 November 2011 in Cell Cycle
Verified
Journal Article
Closed access
PLPaolo Latini
Paolo Latini
MFMattia Frontini
Mattia Frontini
MCManuela Caputo
Manuela Caputo
Juraj GreganJuraj Gregan
Juraj Gregan
LCLubos Cipak
Lubos Cipak
LSLuca Proietti De Santis
Luca Proietti De Santis
Mutations in Cockayne syndrome (CS) A and B genes (CSA and CSB) result in a rare genetic disease that affects the development and homeostasis of a wide range of tissues and organs. We previously correlated the degenerative phenotype of patients to the enhanced apoptotic response, exhibited by CS cells, which is associated with the exceptional induction of p53 protein, upon a variety of stress stimuli. Here we showed that the elevated and persistent levels of p53 displayed by CS cells are due to the insufficient ubiquitination of the p53 protein. We further demonstrated that CSA and CSB proteins associate in a unique complex with p53 and Mdm2; this interaction greatly stimulates the ubiquitination of p53 in an Mdm2-dependent manner. Tandem affinity purification and immunoprecipitations combined with mass spectrometry studies indicate that CSA and CSB associate within a Cullin Ring Ubiquitin Ligase complex responsible, under certain circumstances, for p53 ubiquitination. This study identifies CSA and CSB as...

1 March 2018 in Current Genetics
Verified
Journal Article
Closed access
PDF file
BMB. Mikolaskova
B. Mikolaskova
MJM. Jurcik
M. Jurcik
ICI. Cipakova
I. Cipakova
MKM. Kretova
M. Kretova
Miroslav ChovanecMiroslav Chovanec
Miroslav Chovanec
LCLubos Cipak
Lubos Cipak

1 January 2003 in Leukemia Research
Verified
Journal Article
Closed access
LCLubos Cipak
Lubos Cipak
PRPeter Rauko
Peter Rauko
EMEva Miadoková
Eva Miadoková
IČIngrid Čipáková
Ingrid Čipáková
LNLadislav Novotný
Ladislav Novotný

3 May 2007 in Nature Protocols
Verified
Journal Article
Open access
PDF file
Juraj GreganJuraj Gregan
Juraj Gregan
CRChristian G Riedel
Christian G Riedel
MPMark Petronczki
Mark Petronczki
LCLubos Cipak
Lubos Cipak
CRCornelia Rumpf
Cornelia Rumpf
KNKim Nasmyth
Kim Nasmyth
Tandem affinity purification (TAP) is a generic two-step affinity purification protocol for isolation of TAP-tagged proteins together with associated proteins. We used bacterial artificial chromosome to heterologously express TAP-tagged murine Sgo1 protein in human HeLa cells. This allowed us to test the functionality of the Sgo1-TAP protein by RNA interference-mediated depletion of the endogenous human Sgo1. Here, we present an optimized protocol for purification of TAP-tagged Sgo1 protein as well as KIAA1387 from HeLa cells with detailed instructions. The purification protocol can be completed in 1 day and it should be applicable to other proteins.