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The recombinant C-terminus of the human MUC2 mucin forms dimers in Chinese-hamster ovary cells and heterodimers with full-length MUC2 in LS 174T cells.

Lidell, Martin, 1970 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Johansson, Malin E V, 1971 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Mörgelin, Matthias (författare)
Lund University,Lunds universitet,Infektionsmedicin,Sektion III,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Infection Medicine (BMC),Section III,Department of Clinical Sciences, Lund,Faculty of Medicine
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Asker, Noomi, 1968 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Gum, James R (författare)
Kim, Young S (författare)
Hansson, Gunnar C., 1951 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
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 (creator_code:org_t)
2003
2003
Engelska.
Ingår i: The Biochemical journal. - 0264-6021. ; 372:Pt 2, s. 335-45
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The entire cDNA corresponding to the C-terminal cysteine-rich domain of the human MUC2 apomucin, after the serine- and threonine-rich tandem repeat, was expressed in Chinese-hamster ovary-K1 cells and in the human colon carcinoma cell line, LS 174T. The C-terminus was expressed as a fusion protein with the green fluorescent protein and mycTag sequences and the murine immunoglobulin kappa-chain signal sequence to direct the protein to the secretory pathway. Pulse-chase studies showed a rapid conversion of the C-terminal monomer into a dimer in both Chinese-hamster ovary-K1 and LS 174T cells. Disulphide-bond-stabilized dimers secreted into the media of both cell lines had a higher apparent molecular mass compared with the intracellular forms. The MUC2 C-terminus was purified from the spent culture medium and visualized by molecular electron microscopy. The dimer nature of the molecule was visible clearly and revealed that each monomer was attached to the other by a large globular domain. Gold-labelled antibodies against the mycTag or green fluorescent protein revealed that these were localized to the ends opposite to the parts responsible for the dimerization. The C-terminus expressed in LS 174T cells formed heterodimers with the full-length wild-type MUC2, but not with the MUC5AC mucin, normally expressed in LS 174T cells. The homodimers of the MUC2 C-termini were secreted continuously from the LS 174T cells, but no wild-type MUC2 secretion has been observed from these cells. This suggests that the information for sorting the MUC2 mucin into the regulated secretory pathway in cells having this ability is present in parts other than the C-terminus of MUC2.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Animals
Blotting
Western
CHO Cells
Colonic Neoplasms
chemistry
metabolism
Cricetinae
DNA Primers
chemistry
Dimerization
Disulfides
metabolism
Electrophoresis
Polyacrylamide Gel
Gastric Mucins
chemistry
metabolism
Glycoside Hydrolases
metabolism
Glycosylation
Green Fluorescent Proteins
Humans
Hydrofluoric Acid
pharmacology
Immunoglobulin Isotypes
metabolism
Luminescent Proteins
metabolism
Microscopy
Electron
Mucin 5AC
Mucin-2
Mucins
genetics
immunology
metabolism
Mutagenesis
Site-Directed
Plasmids
Polymerase Chain Reaction
Precipitin Tests
Proto-Oncogene Proteins c-myc
metabolism
Recombinant Fusion Proteins
Transfection
mucin
endoplasmic reticulum
electron microscopy
Chinese-hamster ovary cell
dimerization

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