Internal deletions of the human interleukin-6 (IL-6) cDNA have been generated in the region encoding residues 29 to 42. Mutant proteins were produced by in vitro transcription-translation or in Escherichia coli and tested for their biological activity using the hybridoma growth factor (HGF) assay or a transcriptional activation assay on human hepatoma cells. The folding of the mutants was also checked by immunoprecipitation with conformation-specific monoclonal antibodies. The results show that only residues 29 to 34 are crucial for IL-6 activity and that the first two amino acids are probably involved in the definition of the IL-6 active site
AbstractA model of the tertiary structure of human IL-6, derived from the crystal-structure of granu...
A recombinant human interleukin-6 mutant with enhanced conformational stability toward denaturant wa...
AbstractC-terminally deleted analogs of human interleukin-6 (IL-6) have been constructed at the cDNA...
AbstractInternal deletions of the human interleukin-6 (IL-6) cDNA have been generated in the region ...
AbstractInternal deletions of the human interleukin-6 (IL-6) cDNA have been generated in the region ...
Three internal-amino acid deletions of amino acids 171-179 of human interleukin 6 (IL-6) were introd...
Three internal-amino acid deletions of amino acids 171-179 of human interleukin 6 (IL-6) were introd...
By cDNA mutagenesis, we have constructed internal and C-terminal deletions (delta 21-51, delta 52-97...
AbstractWe have constructed on the cDNA level deletion mutants of human interleukin-6 lacking one, t...
AbstractAmino acid substitutions of human interleukin-6 (IL-6) were performed. Single substitution M...
A mutant species of the 185-residue chain of human interleukin-6 lacking 22-residues at its N-termin...
AbstractThirteen point mutations of human interleukin-6 at the C-terminus were constructed at the cD...
The multifunctional cytokine interleukin-6 (IL-6) is a single polypeptide chain consisting of 184 am...
AbstractSite-directed mutagenesis of two sets of three periodic leucine residues which appear at eve...
AbstractC-terminally deleted analogs of human interleukin-6 (IL-6) have been constructed at the cDNA...
AbstractA model of the tertiary structure of human IL-6, derived from the crystal-structure of granu...
A recombinant human interleukin-6 mutant with enhanced conformational stability toward denaturant wa...
AbstractC-terminally deleted analogs of human interleukin-6 (IL-6) have been constructed at the cDNA...
AbstractInternal deletions of the human interleukin-6 (IL-6) cDNA have been generated in the region ...
AbstractInternal deletions of the human interleukin-6 (IL-6) cDNA have been generated in the region ...
Three internal-amino acid deletions of amino acids 171-179 of human interleukin 6 (IL-6) were introd...
Three internal-amino acid deletions of amino acids 171-179 of human interleukin 6 (IL-6) were introd...
By cDNA mutagenesis, we have constructed internal and C-terminal deletions (delta 21-51, delta 52-97...
AbstractWe have constructed on the cDNA level deletion mutants of human interleukin-6 lacking one, t...
AbstractAmino acid substitutions of human interleukin-6 (IL-6) were performed. Single substitution M...
A mutant species of the 185-residue chain of human interleukin-6 lacking 22-residues at its N-termin...
AbstractThirteen point mutations of human interleukin-6 at the C-terminus were constructed at the cD...
The multifunctional cytokine interleukin-6 (IL-6) is a single polypeptide chain consisting of 184 am...
AbstractSite-directed mutagenesis of two sets of three periodic leucine residues which appear at eve...
AbstractC-terminally deleted analogs of human interleukin-6 (IL-6) have been constructed at the cDNA...
AbstractA model of the tertiary structure of human IL-6, derived from the crystal-structure of granu...
A recombinant human interleukin-6 mutant with enhanced conformational stability toward denaturant wa...
AbstractC-terminally deleted analogs of human interleukin-6 (IL-6) have been constructed at the cDNA...