蛋白质工程增强Fab功能的基础研究

IF 0.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Hitomi Nakamura
{"title":"蛋白质工程增强Fab功能的基础研究","authors":"Hitomi Nakamura","doi":"10.1248/yakushi.24-00195","DOIUrl":null,"url":null,"abstract":"<p><p>Antigen-binding fragments (Fab) are a type of antibody fragment that contains an antigen-binding site in a therapeutic antibody format. To further improve their utility as therapeutic antibodies, this study aimed to enhance Fab functionality through protein engineering. A Fab expression system using the yeast Pichia pastoris was constructed, and recombinant Fabs were efficiently prepared. Second, a Fab mutant suitable for conjugation with polyethylene glycol (PEG) was generated to increase the serum half-life of the Fab. The interchain disulfide bond normally formed at the C-terminus (H: Cys224-L: Cys214) was shifted to a novel position (H: Cys177-L: Cys160), allowing a free cysteine residue at the C-terminus to be used for site-directed PEGylation without conformational destabilization of the Fab. The prepared PEGylated Fab displayed an increased serum half-life. Several additional sites for the introduction of interchain disulfide bonds, which contribute to conformational stability, have been identified in the Fab constant region, and a Fab with an N-glycosylation site introduced at position 178 of its heavy chain (H: L178N) was expressed in P. pastoris. The high-mannose type N-glycan attached to Fab showed the inhibited Fab aggregation under pH shift-induced stress, and the immunogenicity of the glycosylated Fab was lower than that of the wild-type Fab. These protein engineering results are expected to contribute to the design of Fab molecules with increased functional value and greater safety.</p>","PeriodicalId":23810,"journal":{"name":"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan","volume":"145 5","pages":"395-401"},"PeriodicalIF":0.2000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Fundamental Research into Enhancing Fab Functionality by Protein Engineering].\",\"authors\":\"Hitomi Nakamura\",\"doi\":\"10.1248/yakushi.24-00195\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Antigen-binding fragments (Fab) are a type of antibody fragment that contains an antigen-binding site in a therapeutic antibody format. To further improve their utility as therapeutic antibodies, this study aimed to enhance Fab functionality through protein engineering. A Fab expression system using the yeast Pichia pastoris was constructed, and recombinant Fabs were efficiently prepared. Second, a Fab mutant suitable for conjugation with polyethylene glycol (PEG) was generated to increase the serum half-life of the Fab. The interchain disulfide bond normally formed at the C-terminus (H: Cys224-L: Cys214) was shifted to a novel position (H: Cys177-L: Cys160), allowing a free cysteine residue at the C-terminus to be used for site-directed PEGylation without conformational destabilization of the Fab. The prepared PEGylated Fab displayed an increased serum half-life. Several additional sites for the introduction of interchain disulfide bonds, which contribute to conformational stability, have been identified in the Fab constant region, and a Fab with an N-glycosylation site introduced at position 178 of its heavy chain (H: L178N) was expressed in P. pastoris. The high-mannose type N-glycan attached to Fab showed the inhibited Fab aggregation under pH shift-induced stress, and the immunogenicity of the glycosylated Fab was lower than that of the wild-type Fab. These protein engineering results are expected to contribute to the design of Fab molecules with increased functional value and greater safety.</p>\",\"PeriodicalId\":23810,\"journal\":{\"name\":\"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan\",\"volume\":\"145 5\",\"pages\":\"395-401\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1248/yakushi.24-00195\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1248/yakushi.24-00195","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

抗原结合片段(Fab)是一种含有治疗性抗体形式的抗原结合位点的抗体片段。为了进一步提高其作为治疗性抗体的效用,本研究旨在通过蛋白质工程增强Fab的功能。利用毕赤酵母构建了Fab表达体系,高效制备了重组Fab。其次,产生适合与聚乙二醇(PEG)偶联的Fab突变体,以增加Fab的血清半衰期。通常在c端形成的链间二硫键(H: Cys224-L: Cys214)被转移到一个新的位置(H: Cys177-L: Cys160),允许c端的游离半胱氨酸残基用于定点PEGylation,而不会破坏Fab的构象稳定性。制备的PEGylated Fab显示血清半衰期增加。在Fab恒定区已经确定了几个额外的引入有助于构象稳定性的链间二硫键的位点,并且在P. pastoris中表达了在其重链(H: L178N)的第178位引入n -糖基化位点的Fab。高甘露糖型n -聚糖在pH漂移诱导的胁迫下,Fab的聚集受到抑制,糖基化后的Fab的免疫原性低于野生型Fab。这些蛋白质工程研究成果有望为设计具有更高功能价值和更高安全性的Fab分子做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Fundamental Research into Enhancing Fab Functionality by Protein Engineering].

Antigen-binding fragments (Fab) are a type of antibody fragment that contains an antigen-binding site in a therapeutic antibody format. To further improve their utility as therapeutic antibodies, this study aimed to enhance Fab functionality through protein engineering. A Fab expression system using the yeast Pichia pastoris was constructed, and recombinant Fabs were efficiently prepared. Second, a Fab mutant suitable for conjugation with polyethylene glycol (PEG) was generated to increase the serum half-life of the Fab. The interchain disulfide bond normally formed at the C-terminus (H: Cys224-L: Cys214) was shifted to a novel position (H: Cys177-L: Cys160), allowing a free cysteine residue at the C-terminus to be used for site-directed PEGylation without conformational destabilization of the Fab. The prepared PEGylated Fab displayed an increased serum half-life. Several additional sites for the introduction of interchain disulfide bonds, which contribute to conformational stability, have been identified in the Fab constant region, and a Fab with an N-glycosylation site introduced at position 178 of its heavy chain (H: L178N) was expressed in P. pastoris. The high-mannose type N-glycan attached to Fab showed the inhibited Fab aggregation under pH shift-induced stress, and the immunogenicity of the glycosylated Fab was lower than that of the wild-type Fab. These protein engineering results are expected to contribute to the design of Fab molecules with increased functional value and greater safety.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.60
自引率
0.00%
发文量
169
审稿时长
1 months
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信