Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2002-1-24
pubmed:abstractText
Dynamic changes in intracellular free Ca(2+) concentrations ([Ca(2+)](i)s) control many important cellular events, including binding of Ca(2+)-calmodulin (Ca(2+)-CaM) and phosphorylation by protein kinase C (PKC). The two signals compete for the same domains in certain substrates, such as myristoylated alanine-rich PKC-substrate (MARCKS). To observe the convergence and relative time of arrival of CaM and PKC signals at their shared domain of MARCKS, we need to image cells that are loaded with more than two fluorescent dyes at a reasonable speed. We have developed a simple and powerful multicolor imaging system using conventional fluorescence microscopy. The epifluorescence configuration uses a glass reflector and rotating filter wheels for excitation and emission paths. As it is free of dichroic (multichroic) mirrors, multiple fluorescence images can be acquired rapidly regardless of the colors of fluorophores. We visualized Ca(2+)-CaM and PKC together with the dynamics of their common target, MARCKS, in single live cells. Receptor-activation resulted in translocation of MARCKS from the plasma membrane to cytosol through its phosphorylation by PKC. By observing fluorescence resonance energy transfer, we also obtained direct evidence that Ca(2+)-CaM binds MARCKS to drag it away from the membrane in circumstances when Ca(2+)-mobilization predominates over PKC activation.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-10051607, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-10074454, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-10088994, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-10840037, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-11045004, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-11175733, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-1874734, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-2557340, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-7559616, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-7836403, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-7961759, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-8420923, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-8861953, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-9278050, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-9669950, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-9759496, http://linkedlifedata.com/resource/pubmed/commentcorrection/11806947-9814702
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/Calmodulin, http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes, http://linkedlifedata.com/resource/pubmed/chemical/Glucosidases, http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes, http://linkedlifedata.com/resource/pubmed/chemical/Luminescent Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PRKCSH protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/myristoylated alanine-rich C..., http://linkedlifedata.com/resource/pubmed/chemical/protein kinase C gamma
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0006-3495
pubmed:author
pubmed:issnType
Print
pubmed:volume
82
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1076-85
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11806947-Calcium, pubmed-meshheading:11806947-Calmodulin, pubmed-meshheading:11806947-Fluorescent Dyes, pubmed-meshheading:11806947-Glucosidases, pubmed-meshheading:11806947-Green Fluorescent Proteins, pubmed-meshheading:11806947-HeLa Cells, pubmed-meshheading:11806947-Humans, pubmed-meshheading:11806947-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:11806947-Isoenzymes, pubmed-meshheading:11806947-Light, pubmed-meshheading:11806947-Luminescent Proteins, pubmed-meshheading:11806947-Membrane Proteins, pubmed-meshheading:11806947-Microscopy, Fluorescence, pubmed-meshheading:11806947-Phosphoproteins, pubmed-meshheading:11806947-Phosphorylation, pubmed-meshheading:11806947-Protein Binding, pubmed-meshheading:11806947-Protein Kinase C, pubmed-meshheading:11806947-Protein Transport, pubmed-meshheading:11806947-Recombinant Fusion Proteins, pubmed-meshheading:11806947-Time Factors
pubmed:year
2002
pubmed:articleTitle
Multicolor imaging of Ca(2+) and protein kinase C signals using novel epifluorescence microscopy.
pubmed:affiliation
Laboratory for Cell Function and Dynamics, Advanced Technology Development Center, Brain Science Institute, RIKEN, 2-1 Hirosawa, Wako-city, Saitama, 351-0198, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't