Literature DB >> 6430761

The gamma 1 heavy-chain disease FOR protein is present in two molecular forms.

J Zikán, L Rozprimová, J Novotný.   

Abstract

Heavy chain disease proteins (FOR) were isolated from human plasma. These proteins were also detected immunochemically in the urine of the patient. The proteins were disulphide-linked Fc-like dimers with molar mass 64.2 kg/mol and sedimentation rate S020,W = 0.356 ps (3.56 S). Similar amounts of aspartic acid and pyroglutamic acid were found at the N-terminus. After cyanogen bromide cleavage of the FOR proteins, three peptides were isolated and their amino acid composition and partial amino acid sequence was determined. We suggest that two Fc-like proteins of similar sizes are present in the plasma: (1) the first with N-terminal aspartic acid corresponding to position 221 of gamma 1 EU chain and (2) the second with N-terminal pyroglutamic acid. The first protein and small amounts of related low-molar mass fragments found also in the plasma could be degradation products of the second protein. Evidence is given on structural differences between the FOR proteins and the corresponding portion of the gamma 1 EU chain.

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Year:  1984        PMID: 6430761     DOI: 10.1007/bf02877317

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.099


  34 in total

1.  Domains and the hinge region of an immunoglobulin heavy chain are encoded in separate DNA segments.

Authors:  H Sakano; J H Rogers; K Hüppi; C Brack; A Traunecker; R Maki; R Wall; S Tonegawa
Journal:  Nature       Date:  1979-02-22       Impact factor: 49.962

2.  The separation of N-2:4-dinitrophenly amino-acids on paper chromatograms.

Authors:  S BLACKBURN; A G LOWTHER
Journal:  Biochem J       Date:  1951-01       Impact factor: 3.857

3.  A technique for the detection of deleted immunoglobulin heavy chains.

Authors:  B Frangione
Journal:  Biochemistry       Date:  1973-08-14       Impact factor: 3.162

4.  The molecular defect in a protein (CRA) found in gamma-1 heavy chain disease, and its genetic implications.

Authors:  E C Franklin; B Frangione
Journal:  Proc Natl Acad Sci U S A       Date:  1971-01       Impact factor: 11.205

5.  The covalent structure of an entire gammaG immunoglobulin molecule.

Authors:  G M Edelman; B A Cunningham; W E Gall; P D Gottlieb; U Rutishauser; M J Waxdal
Journal:  Proc Natl Acad Sci U S A       Date:  1969-05       Impact factor: 11.205

6.  A gamma l heavy-chain disease protein *EST) lacking the entire VH and CHl domains.

Authors:  J Biewenga; B Frangione; E C Franklin; E van Loghem
Journal:  Scand J Immunol       Date:  1980       Impact factor: 3.487

7.  Human heavy chain disease protein WIS: implications for the organization of immunoglobulin genes.

Authors:  E C Franklin; F Prelli; B Frangione
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

8.  [The rule of antibody structure. The primary structure of a monoclonal IgG1 immunoglobulin (myeloma protein Nie). III. The chymotryptic peptides of the H-chain, alignment of the tryptic peptides and discussion of the complete structure].

Authors:  H Ponstingl; N Hilschmann
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1976-11

9.  The N-terminal sequence of the heavy chain of rabbit immunoglobulin IgG.

Authors:  J M Wilkinson; E M Press; R R Porter
Journal:  Biochem J       Date:  1966-08       Impact factor: 3.857

10.  THE MOLECULAR WEIGHT OF ANTIBODIES.

Authors:  E A Kabat
Journal:  J Exp Med       Date:  1939-01-01       Impact factor: 14.307

View more
  1 in total

1.  [Gamma 1 heavy chain disease with immune vasculitis and rheumatoid arthritis].

Authors:  W Stühlinger; K Berek; A Lapin; E Jaschke; D Pastner
Journal:  Klin Wochenschr       Date:  1987-04-15
  1 in total

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