Hammer J, Takacs B, Sinigaglia F
Department of Biology, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
J Exp Med. 1992 Oct 1;176(4):1007-13. doi: 10.1084/jem.176.4.1007.
Oligonucleotides encoding peptides known to bind to HLA-DR1 molecules have been inserted into the gene III of filamentous M13 phages. DR1 molecules purified from human lymphoblastoid cell lines could specifically bind to these peptide sequences expressed on the phage surface. A M13 phage peptide library was next constructed and screened with DR1 molecules. After four rounds of selection, more than 80% of the phages were able to bind to DR1. Competition experiments with both isolated phages and corresponding synthetic peptides showed that the binding was specific. Sequence analysis of the peptide encoding region of 60 phages binding to DR1 molecules and comparison with phages of the original library revealed two potential anchor positions. The first was an aromatic residue (Tyr, Phe, or Trp) at the NH2 terminus of the peptide sequences, and the second was located three residues downstream and consisted of Met or Leu. In addition, the negatively charged amino acids Asp and Glu were mostly excluded from the DR1 binding sequences, and the small amino acid residues Gly and Ala were enriched at position 6. As for DR1, this approach should enable one to easily determine the binding motifs of other MHC class II alleles and isotypes. Furthermore, it could have interesting applications in the design of major histocompatibility complex-specific antagonists.
已知能与HLA - DR1分子结合的肽的编码寡核苷酸已被插入丝状M13噬菌体的基因III中。从人淋巴母细胞系中纯化的DR1分子能特异性结合在噬菌体表面表达的这些肽序列。接下来构建了一个M13噬菌体肽库并用DR1分子进行筛选。经过四轮筛选,超过80%的噬菌体能够与DR1结合。用分离出的噬菌体和相应的合成肽进行的竞争实验表明这种结合是特异性的。对60个与DR1分子结合的噬菌体的肽编码区进行序列分析,并与原始文库的噬菌体进行比较,发现了两个潜在的锚定位点。第一个是肽序列NH2末端的一个芳香族残基(酪氨酸、苯丙氨酸或色氨酸),第二个位于下游三个残基处,由甲硫氨酸或亮氨酸组成。此外,带负电荷的氨基酸天冬氨酸和谷氨酸大多被排除在DR1结合序列之外,小氨基酸残基甘氨酸和丙氨酸在第6位富集。对于DR1而言,这种方法应该能使人们轻松确定其他MHC II类等位基因和同种型的结合基序。此外,它在主要组织相容性复合体特异性拮抗剂的设计中可能有有趣的应用。