Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM), México D,F,, Ciudad Universitaria, 04510, México.
Vet Res. 2011 Jul 22;42(1):87. doi: 10.1186/1297-9716-42-87.
Using phage display and IgG of a goat infected with Caprine Arthritis Encephalitis Virus (CAEV) we obtained families of 7 mer constrained peptides with consensus motifs LxSDPF/Y and SWN/KHWSY and mapped the epitopes mimicked by them at the Env 6-LISDPY-11 and 67-WNTYHW-72 sites of the mature gp135 amino acid sequence. The first epitope fell into the N-terminal immunogenic aa1-EDYTLISDPYGFS- aa14 site identified previously with a synthetic peptide approach; the second epitope has not been described previously. The first epitope is mostly conserved across CAEV isolates whereas the second newly described epitope is extremely conserved in Small Ruminant Lentiviruses env sequences. As being immunodominant, the epitopes are candidate targets for mimotope-mediated diagnosis and/or neutralization.
利用噬菌体展示和感染 Caprine Arthritis Encephalitis Virus (CAEV) 的山羊 IgG,我们获得了具有共识基序 LxSDPF/Y 和 SWN/KHWSY 的 7 mer 约束肽家族,并绘制了它们在成熟 gp135 氨基酸序列的 Env 6-LISDPY-11 和 67-WNTYHW-72 位点模拟的表位。第一个表位落入先前用合成肽方法鉴定的 N 端免疫原性 aa1-EDYTLISDPYGFS-aa14 位点;第二个表位以前没有描述过。第一个表位在 CAEV 分离株中大多保守,而第二个新描述的表位在小反刍动物 Lentiviruses env 序列中极其保守。作为免疫优势表位,这些表位是模拟表位介导的诊断和/或中和的候选靶标。