Lie B L, Tunemoto D, Hemmi H, Mizukami Y, Fukuda H, Kikuchi H, Kato S, Numao N
Sagami Chemical Research Center, Kanagawa, Japan.
Biochem Biophys Res Commun. 1992 Oct 30;188(2):503-9. doi: 10.1016/0006-291x(92)91084-4.
We have synthesized a series of peptides, which cover almost the whole range of the N-terminal extracellular domain of human 55kDa TNF receptor (55kDa TNF-R). The peptides were examined for the binding activity to TNF by solid phase binding assay and for the inhibition of TNF cytotoxicity to mouse L-M cells. The peptide 159-178 exhibited remarkably higher binding activity to TNF than other peptides did. The specificity of the TNF binding to the peptides was confirmed by their inability to bind other cytokines. The peptide 159-178 also inhibited TNF cytotoxicity. These results indicate that the specific binding site of 55kDa TNF-R to TNF might reside within the peptide segment of amino acid numbers 159 to 178 in the N-terminal extracellular domain.
我们合成了一系列肽段,这些肽段几乎覆盖了人55kDa肿瘤坏死因子受体(55kDa TNF-R)N端细胞外结构域的整个范围。通过固相结合试验检测这些肽段与肿瘤坏死因子(TNF)的结合活性,并检测其对TNF对小鼠L-M细胞细胞毒性的抑制作用。肽段159-178对TNF的结合活性明显高于其他肽段。TNF与这些肽段结合的特异性通过它们不能与其他细胞因子结合得到证实。肽段159-178也能抑制TNF的细胞毒性。这些结果表明,55kDa TNF-R与TNF的特异性结合位点可能位于N端细胞外结构域中氨基酸编号为159至178的肽段内。