流感病毒血凝素和人类蛋白质中连续氨基酸的相同子序列

J. Weltman
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摘要

背景:流感病毒是世界范围内的一个重大公共卫生问题。加深对病毒基本生物学的了解可能有助于开发更有效的抗流感预防和治疗方法。方法:利用H1N1和H3N2流感病毒血凝素中出现的特定氨基酸子序列,联合检测人蛋白中的这些子序列。只有包含至少5个连续氨基酸的子序列才被考虑进行进一步研究。结果:10个H1N1血凝素氨基酸子序列和9个H3N2血凝素氨基酸子序列也存在于人源蛋白中。选择的子序列长度从5个连续氨基酸到8个连续氨基酸不等。结论:流感血凝素和人蛋白中氨基酸序列的共同出现可能有助于解释当前抗流感疫苗相对较低的疗效。本文提出,联合子序列的识别可能有助于改进抗流感治疗药物,特别是抗流感疫苗的设计。
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Identical Subsequences of Contiguous Amino Acids in Influenza Virus Hemagglutinin and in Human Proteins
Background: Influenza virus is a significant public health problem throughout the world. Increased insight into the basic biology of the virus may enable the development of more effective anti-influenza preventives and therapeutics. Methodology: The occurrence of specific amino acid subsequences in H1N1 and H3N2 influenza virus hemagglutinins was used for joint detection of those subsequences in human proteins. Only subsequences consisting of at least 5 contiguous amino acids were considered for further study. Results: Ten H1N1 hemagglutinin amino acid subsequences and nine H3N2 hemagglutinin amino subsequences were identified as also occurring in proteins of human origin. The length of the subsequences selected for further study, ranged from 5 contiguous amino acids to 8 contiguous amino acids. Conclusion: The joint occurrence of amino acid subsequences in influenza hemagglutinins and in human proteins may help explain the relatively low efficacy of current anti-influenza vaccines. It is proposed that the identification of the joint subsequences may be useful for the improved design of anti-influenza therapeutics and especially anti-influenza vaccines.
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