Wu Guang, Yan Shaomin
DreamSciTech Consulting Co. Ltd., 301, Building 12, Nanyou A-zone, Jainnan Road, CN-518054, Shenzhen, PR China.
Peptides. 2003 Dec;24(12):1837-45. doi: 10.1016/j.peptides.2003.10.008.
In this study, we analyzed the amino acid pairs affected by mutations in two spike proteins from human coronavirus strains 229E and OC43 by means of random analysis in order to gain some insight into the possible mutations in the spike protein from SARS-CoV. The results demonstrate that the randomly unpredictable amino acid pairs are more sensitive to the mutations. The larger is the difference between actual and predicted frequencies, the higher is the chance of mutation occurring. The effect induced by mutations is to reduce the difference between actual and predicted frequencies. The amino acid pairs whose actual frequencies are larger than their predicted frequencies are more likely to be targeted by mutations, whereas the amino acid pairs whose actual frequencies are smaller than their predicted frequencies are more likely to be formed after mutations. These findings are identical to our several recent studies, i.e. the mutations represent a process of degeneration inducing human diseases.
在本研究中,我们通过随机分析方法,对来自人类冠状病毒株229E和OC43的两种刺突蛋白中受突变影响的氨基酸对进行了分析,以便深入了解严重急性呼吸综合征冠状病毒(SARS-CoV)刺突蛋白中可能发生的突变。结果表明,随机不可预测的氨基酸对对突变更为敏感。实际频率与预测频率之间的差异越大,发生突变的可能性就越高。突变所诱导的效应是减小实际频率与预测频率之间的差异。实际频率大于其预测频率的氨基酸对更有可能成为突变的靶点,而实际频率小于其预测频率的氨基酸对更有可能在突变后形成。这些发现与我们最近的几项研究一致,即突变代表了一个导致人类疾病的退化过程。