基因治疗制品质量评价技术与方法专栏(二)

不同血清型腺相关病毒衣壳蛋白氨基酸残基序列分析*

展开
  • 1.沈阳药科大学,沈阳 117004;
    2.中国食品药品检定研究院,北京 100050
第一作者 侯宗文 Tel:(010)67095162;E-mail:h9812082022@163.com
秦 玺 Tel:(010)67095426;E-mail:qinxi@nifdc.org.cn
** 史新昌 Tel:(010)67095426;E-mail:shixc@nifdc.org.cn
张怡轩 Tel: 18640553526;E-mail:zhangyxzsh@163.com

收稿日期: 2023-03-15

  网络出版日期: 2024-06-21

基金资助

* 北京市科技计划资助(2021YFF0600804)

Sequence analysis of amino acid residues in adeno-associated virus capsid protein of different serotypes*

Expand
  • 1. Shenyang Pharmaceutical University, Shenyang 117004, China;
    2. National Institutes of Food and Drug Control, Beijing 100050, China

Received date: 2023-03-15

  Online published: 2024-06-21

摘要

目的:分析不同血清型腺相关病毒衣壳蛋白(VP1)氨基酸残基序列,建立相似性比较方法和数据库,预测VP1氨基酸残基序列突变后可能隶属的血清型。方法:对不同血清型腺相关病毒VP1氨基酸残基序列分析,找出共同序列,并对序列进行对齐。分别对疏水氨基酸残基、亲水氨基酸残基和酸/碱氨基酸残基进行单独赋值,赋值参数包括侧链长度、基团数量和解离/结合强度等,再用相关系数法和差值法计算相似度。规定全局电荷决定界值,判断电荷的变化是否会引起蛋白质周围电场的显著变化。最后综合考虑四者的关系,给出与已知血清型VP1氨基酸残基序相似度。通过其他已知血清型的VP1氨基酸残基序进行验证。结果:基本上可以区分不同的血清型,并且对相同血清型中的不同亚型具有一定的容忍度。结论:对腺相关病毒衣壳蛋白VP1氨基酸残基序列与其血清型间的联系进行了探讨,希望对重组腺相关病毒为载体的基因治疗研发提供支持。

本文引用格式

侯宗文, 秦玺, 陶磊, 史新昌, 张怡轩 . 不同血清型腺相关病毒衣壳蛋白氨基酸残基序列分析*[J]. 药物分析杂志, 2023 , 43(12) : 2017 -2024 . DOI: 10.16155/j.0254-1793.2023.12.04

Abstract

Objective: To analyze the amino acid residue sequences of adeno-associated virus capsid protein (VP1) of different serotypes, and establish the similarity comparison method and database, and to predict the serotypes that VP1 may belong to after amino acid residue sequence mutation. Methods: The amino acid residues of VP1 of adeno-associated virus of different serotypes were analyzed to find out a common sequence, and the sequences were aligned. The hydrophobic amino acid residues, hydrophilic amino acid residues and acid/base amino acid residues were assigned separately. The assignment parameters included side chain length, group number and dissociation/binding strength. Then the similarity was calculated by correlation coefficient method and difference method. The global charge was defined to determine the boundary value, and determine whether the change of charge will cause a significant change in the electric field around the protein. Finally, considering the relationship of the four, the similarity with the known serological sequences was given. The protein amino acid sequences of other known serotypes were verified. Results: Basically, different serotypes could be distinguished, and different subtypes of the same serotype have a certain tolerance. Conclusion: The relationship between the amino acid residues sequence of adeno-associated VP1 and its serotype was discussed, hoping to provide support for the research and development of recombinant adeno-associated virus as a vector for gene therapy.

参考文献

[1] 国家药品监督管理局药品审评中心. 体内基因治疗产品药学研究与评价技术指导原则(试行)[EB/OL]. (2022-5-26) [2023-06-14]. https://www.cde.org.cn/main/news/viewInfoCommon/c0ec5e347ba84df67bf75e15f6ad3f3f
Enter For Drug Evaluation. Technical Guidelines for Pharmaceutical Research and Evaluation of In Vivo Gene Therapy Products (Trial)[DB/OL]. (2022-5-26) [2023-06-14]. https://www.cde.org.cn/main/news/viewInfoCommon/c0ec5e347ba84df67bf75e15f6ad3f3f
[2] MIETZSCH M, HULLJA, MAKAL VE, et al. Characterization of the serpentine adeno-associated virus (SAAV) capsid structure: receptor interactions and antigenicity[J]. J Virol, 2022, 96(11):e00335
[3] GILES AR, SIMS JJ, TURNER KB, et al. Deamidation of amino acids on the surface of adeno-associated virus capsids leads to charge heterogeneity and altered vector function[J]. Mol Ther, 2018, 26(12):2848
[4] LARGE EE, SILVERIA MA, ZANE GM, et al. Adeno-associated virus (AAV) gene delivery: dissecting molecular interactions upon cell entry[J]. Viruses, 2021, 13(7):1336
[5] HERRMANN AK, GRIMM D. High-throughput dissection of AAV-host interactions: the fast and the curious[J]. Mol Biol, 2018, 430(17):2626
[6] 曹雪涛.医学免疫学[M]. 第6版.北京:人民卫生出版社, 2013: 35
CAO XT, Medical Immunology[M]. 6nd Ed.Beijing:People’s Medical Publishing House, 2013:35
[7] 李响, 史新昌, 范文红, 等. 重组人促红素异构体唾液酸化程度分析[J]. 中国药学杂志, 2018, 53(19):1682
LI X, SHI XC, FAN WH, et al. Estimation of the degree of salivary acidification of recombinant-human-erythropoietin (rhEPO) [J]. Chin Pharm J, 2018, 53(19):1682
[8] 史新昌, 李响, 范文红, 等. 重组白介素-15融合蛋白成像毛细管等电聚焦电泳谱图分析[J]. 中国药学杂志, 2020(9):745
SHI XC, LI X, YU L, et al. Analysis of WCID-cIEF spectrogram of recombinant interleukin-15 fusion protein[J]. Chin Pharm J, 2020 (9):745
[9] 汤其群.生物化学与分子生物学[M]. 上海:复旦大学出版社, 2015:9
TANG QQ.Biochemistry and Molecular Biology[M]. Shanghai:Fudan University Press, 2015:9
[10] 丁明孝, 王喜忠, 张传茂, 等.细胞生物学[M]. 第5版.北京:高等教育出版社, 2020:5
DING MX, WANG XZ, ZHANG CM, et al. Cell Biology[M]. 5nd EG.Beijing:Higher Education Rress, 2020:5
[11] 史新昌, 李响, 于雷, 等. 重组人促红素等电点异构体分子体内活性强度分析[J]. 中国生物制品学杂志, 2020, 133(5):549
SHI XC, LI X, YU L, et al. In vivo biological activity strength of isoelectric point isoform molecules of recombinant human erythropoietin[J]. Chin J Biologicals, 2020, 33(5):549
[12] 林训忠.酸碱度与人体健康[J]. 科技信息, 2013(2):16
LIN XZ.pH and human health[J]. Scientific and technical information, 2013(2):16
[13] MINDELL JA. Lysosomal acidification mechanisms[J]. Annu Rev Physiol, 2012, 74:69
[14] CANTON J, GRINSTEIN S. Measuring lysosomal pH by fluorescence microscopy[J]. Methods Cell Biol, 2015;126:85
[15] BRORSON K, KREJCI S, LEE K, et al. Bracketed generic inactivation of rodent retroviruses by low pH treatment for monoclonal antibodies and recombinant proteins[J]. Biotechnol Bioengin, 2008, 32(3):321
[16] LIU LK, BECKER DF, TANNER JJ. Structure, function, and mechanism of proline utilization A (PutA)[J]. Arch Biochem Biophys, 2017, 632:142
文章导航

/