Wu D G, Wang L H, Chi Y, Sato G H, Sato J D
W. Alton Jones Cell Science Center, Inc., Lake Placid, NY 12946.
Proc Natl Acad Sci U S A. 1990 Apr;87(8):3151-5. doi: 10.1073/pnas.87.8.3151.
An epidermal growth factor (EGF) receptor monoclonal antibody (mAb), mAb LA22, was used to analyze the covalent coupling of human EGF receptors to mouse EGF by the amine-reactive cross-linking agent disuccinimidyl suberate. A soluble Mr 105,000 truncated form of the receptor secreted by A-431 epidermoid carcinoma cells and consisting of the ligand-binding extracellular domain was cross-linked to 125I-labeled EGF. Digestion of this complex with an endoproteinase that specifically cleaves at the COOH side of glutamyl residue released a single radiolabeled glycosylated fragment of Mr 18,000 that reacted with mAb LA22. As the epitope for mAb LA22 resided between Ala-351 and Asp-364 of the mature receptor, this result localized the cross-linked receptor residue(s) to the 47-amino acid interval from Phe-321 to Glu-367. The receptor residue(s) involved in the covalent coupling of rat 125I-labeled transforming growth factor alpha was similarly localized to this region of the receptor. This receptor interval, which included two glycosylated asparaginyl residues at positions 328 and 337, contained but three amino acid residues that were potentially reactive with disuccinimidyl suberate: Lys-332, Lys-333, and Lys-336. Characterization of mAb LA22-reactive 125I-EGF-labeled receptor fragments generated by an endoproteinase specific for the COOH side of lysyl residue placed the NH2 termini of the two smallest fragments between the glycosylated residues Asn-328 and Asn-337. These results indicated that disuccinimidyl suberate cross-linked the NH2 group of EGF residue Asn-1 to the human EGF receptor residue Lys-336. Our results further suggest that EGF and transforming growth factor alpha, two members of the EGF family of peptide growth factors, interact with closely apposed or identical features of the receptor.
使用表皮生长因子(EGF)受体单克隆抗体(mAb)LA22,通过胺反应性交联剂辛二酸二琥珀酰亚胺酯分析人EGF受体与小鼠EGF的共价偶联。由A - 431表皮样癌细胞分泌的、包含配体结合细胞外结构域的可溶性Mr 105,000截短形式的受体与125I标记的EGF交联。用一种在内蛋白酶作用下能在谷氨酰胺残基的COOH侧特异性切割的内蛋白酶消化该复合物,释放出一个Mr 18,000的单一放射性标记糖基化片段,该片段与mAb LA22反应。由于mAb LA22的表位位于成熟受体的Ala - 351和Asp - 364之间,该结果将交联的受体残基定位到从Phe - 321到Glu - 367的47个氨基酸间隔内。参与大鼠125I标记的转化生长因子α共价偶联的受体残基同样定位到受体的该区域。这个受体间隔,包括位置328和337处的两个糖基化天冬酰胺残基,仅包含三个可能与辛二酸二琥珀酰亚胺酯反应的氨基酸残基:Lys - 332、Lys - 333和Lys - 336。对由一种对赖氨酰残基的COOH侧具有特异性的内蛋白酶产生的mAb LA22反应性125I - EGF标记的受体片段的表征,将两个最小片段的NH2末端置于糖基化残基Asn - 328和Asn - 337之间。这些结果表明辛二酸二琥珀酰亚胺酯将EGF残基Asn - 1的NH2基团与人类EGF受体残基Lys - 336交联。我们的结果进一步表明,EGF和转化生长因子α,这两种肽生长因子的EGF家族成员,与受体紧密相邻或相同的特征相互作用。