-
Something wrong with this record ?
Defining the subcellular distribution and metabolic channeling of phosphatidylinositol
JG. Pemberton, YJ. Kim, J. Humpolickova, A. Eisenreichova, N. Sengupta, DJ. Toth, E. Boura, T. Balla,
Language English Country United States
Document type Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1962 to 6 months ago
Freely Accessible Science Journals
from 1962 to 6 months ago
Europe PubMed Central
from 1962 to 6 months ago
Open Access Digital Library
from 1955-01-25
Open Access Digital Library
from 1959-01-01
Open Access Digital Library
from 1962-01-01
PubMed
32211894
DOI
10.1083/jcb.201906130
Knihovny.cz E-resources
- MeSH
- Bacterial Proteins genetics metabolism MeSH
- Biosensing Techniques MeSH
- Cell Membrane metabolism MeSH
- Chlorocebus aethiops MeSH
- COS Cells MeSH
- Phosphatidylinositol Phosphates metabolism MeSH
- Phosphatidylinositols metabolism MeSH
- Type C Phospholipases genetics metabolism MeSH
- HEK293 Cells MeSH
- Intracellular Membranes metabolism MeSH
- Kinetics MeSH
- Microscopy, Confocal MeSH
- Humans MeSH
- Luminescent Proteins genetics metabolism MeSH
- Recombinant Fusion Proteins genetics metabolism MeSH
- Second Messenger Systems MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Comparative Study MeSH
Phosphatidylinositol (PI) is an essential structural component of eukaryotic membranes that also serves as the common precursor for polyphosphoinositide (PPIn) lipids. Despite the recognized importance of PPIn species for signal transduction and membrane homeostasis, there is still a limited understanding of the relationship between PI availability and the turnover of subcellular PPIn pools. To address these shortcomings, we established a molecular toolbox for investigations of PI distribution within intact cells by exploiting the properties of a bacterial enzyme, PI-specific PLC (PI-PLC). Using these tools, we find a minor presence of PI in membranes of the ER, as well as a general enrichment within the cytosolic leaflets of the Golgi complex, peroxisomes, and outer mitochondrial membrane, but only detect very low steady-state levels of PI within the plasma membrane (PM) and endosomes. Kinetic studies also demonstrate the requirement for sustained PI supply from the ER for the maintenance of monophosphorylated PPIn species within the PM, Golgi complex, and endosomal compartments.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20028411
- 003
- CZ-PrNML
- 005
- 20210114153804.0
- 007
- ta
- 008
- 210105s2020 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1083/jcb.201906130 $2 doi
- 035 __
- $a (PubMed)32211894
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Pemberton, Joshua G $u Section on Molecular Signal Transduction, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
- 245 10
- $a Defining the subcellular distribution and metabolic channeling of phosphatidylinositol / $c JG. Pemberton, YJ. Kim, J. Humpolickova, A. Eisenreichova, N. Sengupta, DJ. Toth, E. Boura, T. Balla,
- 520 9_
- $a Phosphatidylinositol (PI) is an essential structural component of eukaryotic membranes that also serves as the common precursor for polyphosphoinositide (PPIn) lipids. Despite the recognized importance of PPIn species for signal transduction and membrane homeostasis, there is still a limited understanding of the relationship between PI availability and the turnover of subcellular PPIn pools. To address these shortcomings, we established a molecular toolbox for investigations of PI distribution within intact cells by exploiting the properties of a bacterial enzyme, PI-specific PLC (PI-PLC). Using these tools, we find a minor presence of PI in membranes of the ER, as well as a general enrichment within the cytosolic leaflets of the Golgi complex, peroxisomes, and outer mitochondrial membrane, but only detect very low steady-state levels of PI within the plasma membrane (PM) and endosomes. Kinetic studies also demonstrate the requirement for sustained PI supply from the ER for the maintenance of monophosphorylated PPIn species within the PM, Golgi complex, and endosomal compartments.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a bakteriální proteiny $x genetika $x metabolismus $7 D001426
- 650 _2
- $a biosenzitivní techniky $7 D015374
- 650 _2
- $a COS buňky $7 D019556
- 650 _2
- $a buněčná membrána $x metabolismus $7 D002462
- 650 _2
- $a Cercopithecus aethiops $7 D002522
- 650 _2
- $a HEK293 buňky $7 D057809
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a intracelulární membrány $x metabolismus $7 D007425
- 650 _2
- $a kinetika $7 D007700
- 650 _2
- $a luminescentní proteiny $x genetika $x metabolismus $7 D008164
- 650 _2
- $a konfokální mikroskopie $7 D018613
- 650 _2
- $a fosfatidylinositolfosfáty $x metabolismus $7 D018129
- 650 _2
- $a fosfatidylinositoly $x metabolismus $7 D010716
- 650 _2
- $a rekombinantní fúzní proteiny $x genetika $x metabolismus $7 D011993
- 650 _2
- $a systémy druhého messengeru $7 D015290
- 650 _2
- $a fosfolipasy typu C $x genetika $x metabolismus $7 D010738
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a Research Support, N.I.H., Extramural $7 D052061
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kim, Yeun Ju $u Section on Molecular Signal Transduction, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
- 700 1_
- $a Humpolickova, Jana $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
- 700 1_
- $a Eisenreichova, Andrea $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
- 700 1_
- $a Sengupta, Nivedita $u Section on Molecular Signal Transduction, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
- 700 1_
- $a Toth, Daniel J $u Section on Molecular Signal Transduction, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
- 700 1_
- $a Boura, Evzen $u Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
- 700 1_
- $a Balla, Tamas $u Section on Molecular Signal Transduction, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
- 773 0_
- $w MED00002575 $t The Journal of cell biology $x 1540-8140 $g Roč. 219, č. 3 (2020)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32211894 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20210105 $b ABA008
- 991 __
- $a 20210114153801 $b ABA008
- 999 __
- $a ok $b bmc $g 1608746 $s 1119591
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 219 $c 3 $e 20200302 $i 1540-8140 $m The Journal of cell biology $n J Cell Biol $x MED00002575
- LZP __
- $a Pubmed-20210105