Department of General Chemistry, Belarussian State Medical University, Minsk 220000, Belarus.
Immunol Invest. 2010;39(6):551-69. doi: 10.3109/08820131003706313.
We used a DiscoTope 1.2 (http://www.cbs.dtu.dk/services/DiscoTope/), Epitopia (http://epitopia.tau.ac.il/) and EPCES (http://www.t38.physik.tu-muenchen.de/programs.htm) algorithms to map discontinuous B-cell epitopes in HIV1 gp120. The most mutable nucleotides in HIV genes are guanine (because of G to A hypermutagenesis) and cytosine (because of C to U and C to A mutations). The higher is the level of guanine and cytosine usage in third (neutral) codon positions and the lower is their level in first and second codon positions of the coding region, the more stable should be an epitope encoded by this region. We compared guanine and cytosine usage in regions coding for five predicted 3D B-cell epitopes of gp120. To make this comparison we used GenBank resource: 385 sequences of env gene obtained from ten HIV1-infected individuals were studied (http://www.barkovsky.hotmail.ru/Data/Seqgp120.htm). The most protected from nonsynonymous nucleotide mutations of guanine and cytosine 3D B-cell epitope is situated in the first conserved region of gp120 (it is mapped from 66th to 86th amino acid residue). We applied a test of variability to confirm this finding. Indeed, the less mutable predicted B-cell epitope is the less variable one. MEGA4 (standard PAM matrix) was used for the alignments and "VVK Consensus" algorithm (http://www.barkovsky.hotmail.ru) was used for the calculations.
我们使用了 DiscoTope 1.2(http://www.cbs.dtu.dk/services/DiscoTope/)、Epitopia(http://epitopia.tau.ac.il/)和 EPCES(http://www.t38.physik.tu-muenchen.de/programs.htm)算法来预测 HIV1 gp120 中的不连续 B 细胞表位。HIV 基因中最易发生突变的核苷酸是鸟嘌呤(由于 G 到 A 的超突变)和胞嘧啶(由于 C 到 U 和 C 到 A 的突变)。第三(中性)密码子位置的鸟嘌呤和胞嘧啶使用率越高,编码区的第一和第二密码子位置的鸟嘌呤和胞嘧啶使用率越低,由该区域编码的表位应该越稳定。我们比较了预测的 gp120 中的五个 3D B 细胞表位编码区的鸟嘌呤和胞嘧啶使用率。为了进行比较,我们使用了 GenBank 资源:从十个 HIV1 感染个体中获得的 385 个 env 基因序列(http://www.barkovsky.hotmail.ru/Data/Seqgp120.htm)。位于 gp120 第一个保守区的 3D B 细胞表位受到鸟嘌呤和胞嘧啶非同义突变的保护最多(它从第 66 位到第 86 位氨基酸残基映射)。我们应用了变异性检验来证实这一发现。事实上,预测的 B 细胞表位越不易变,它就越稳定。MEGA4(标准 PAM 矩阵)用于比对,“VVK 共识”算法(http://www.barkovsky.hotmail.ru)用于计算。