TY - JOUR
T1 - Clonal proteomics
T2 - One gene-family of proteins
AU - Kettman, John R.
AU - Coleclough, Christopher
AU - Frey, Johann Rudolf
AU - Lefkovits, Ivan
PY - 2002
Y1 - 2002
N2 - The work presented here attempts to consolidate our knowledge on cellular transcriptome and proteome. It takes into account that a typical activated cell (lymphocyte) contains 40 000 mRNA molecules at any time, and it represents about 5000 different molecular species of transcripts. Such a cell has about 1 000 000 000 protein molecules, some of them being present at 10 000 000 copies while others at a very low copy number (say 1 to 10 copies per cell). By studying cell free expression of individual cDNA clones (or pools of known complexity) we address to those rare molecular components that will remain undetected by the current analytical means. For our analysis we use cell free translation systems (wheat germ or rabbit reticulocyte origin) and we study polypeptide products originating from intact, or restriction endonuclease-treated cDNA clones. We conclude that in most instances expressed genes yield transcript(s) that translate into several, and often very numerous families of polypeptide species. In our ISODALT two-dimensional gel system we characterize the proteomic profile of the clonal polypeptide families in terms of their molecular mass, charge, multiple products, and appearance.
AB - The work presented here attempts to consolidate our knowledge on cellular transcriptome and proteome. It takes into account that a typical activated cell (lymphocyte) contains 40 000 mRNA molecules at any time, and it represents about 5000 different molecular species of transcripts. Such a cell has about 1 000 000 000 protein molecules, some of them being present at 10 000 000 copies while others at a very low copy number (say 1 to 10 copies per cell). By studying cell free expression of individual cDNA clones (or pools of known complexity) we address to those rare molecular components that will remain undetected by the current analytical means. For our analysis we use cell free translation systems (wheat germ or rabbit reticulocyte origin) and we study polypeptide products originating from intact, or restriction endonuclease-treated cDNA clones. We conclude that in most instances expressed genes yield transcript(s) that translate into several, and often very numerous families of polypeptide species. In our ISODALT two-dimensional gel system we characterize the proteomic profile of the clonal polypeptide families in terms of their molecular mass, charge, multiple products, and appearance.
KW - Cell-free translation
KW - Clonal proteomics
KW - Ordered library
KW - Post-translational modifications
KW - Proteinpaedia
KW - Restriction enzyme mapping
KW - Transcription
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U2 - 10.1002/1615-9861(200206)2:6<624::AID-PROT624>3.0.CO;2-I
DO - 10.1002/1615-9861(200206)2:6<624::AID-PROT624>3.0.CO;2-I
M3 - Article
C2 - 12112841
AN - SCOPUS:0035987415
SN - 1615-9853
VL - 2
SP - 624
EP - 631
JO - Proteomics
JF - Proteomics
IS - 6
ER -