• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

生产具有生物活性的重组人转甲状腺素蛋白,以了解家族性淀粉样多神经病(FAP)的分子基础。

Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP).

作者信息

Furuya H, Saraiva M J, Gawinowicz M A, Alves I L, Costa P P, Sasaki H, Goto I, Sakaki Y

机构信息

Research Laboratory for Genetic Information, Kyushu University, Fukuoka, Japan.

出版信息

Biochemistry. 1991 Mar 5;30(9):2415-21. doi: 10.1021/bi00223a017.

DOI:10.1021/bi00223a017
PMID:1848097
Abstract

Transthyretin (TTR) is a plasma protein interacting with thyroxine T4 and retinol binding protein (RBP). Several variants of TTR with single amino acid substitutions have been identified as the major components of the amyloid fibrils of familial amyloidotic polyneuropathy (FAP), a fetal, autosomal dominant genetic disease. The elucidation of the molecular nature of the variants distinct from that of the wild-type TTR is crucial for understanding the amyloidogenesis in FAP, but our understanding is very poor mainly because of the unavailability of pure variant TTRs. In the present study, we used an Escherichia coli OmpA secretion vector (Ghrayeb et al., 1984) and achieved an effective production of the variant TTRs related to FAP including Met-30, Ile-33, Ala-60, Tyr-77, Met-111, and Ile-122 types. The variant TTRs produced in this system were efficiently secreted to the culture media. The chemical analysis showed that the secreted TTR (Met-30 type) has the same N-terminus as the native one. IEF analyses also indicated that the secreted product is properly processed as assessed by its pI. Furthermore, the secreted TTR was shown to have biological activities, namely, the thyroxin binding activity and the ability to associate with retinol binding protein, indicating that the secreted TTR polypeptide is properly folded. The present work also demonstrated that the processing/secretion of the recombinant TTR molecules in E. coli was strongly affected by single amino acid substitutions.

摘要

转甲状腺素蛋白(TTR)是一种与甲状腺素T4和视黄醇结合蛋白(RBP)相互作用的血浆蛋白。已鉴定出几种具有单个氨基酸取代的TTR变体,它们是家族性淀粉样多神经病(FAP)淀粉样原纤维的主要成分,FAP是一种致死性常染色体显性遗传病。阐明与野生型TTR不同的变体的分子性质对于理解FAP中的淀粉样蛋白生成至关重要,但我们的了解非常有限,主要是因为无法获得纯的变体TTR。在本研究中,我们使用了大肠杆菌OmpA分泌载体(Ghrayeb等人,1984年),并成功有效生产了与FAP相关的变体TTR,包括Met-30、Ile-33、Ala-60、Tyr-77、Met-111和Ile-122类型。在该系统中产生的变体TTR被有效地分泌到培养基中。化学分析表明,分泌的TTR(Met-30型)与天然TTR具有相同的N末端。IEF分析还表明,根据其pI评估,分泌产物得到了正确的加工。此外,分泌的TTR显示具有生物学活性,即甲状腺素结合活性和与视黄醇结合蛋白结合的能力,表明分泌的TTR多肽正确折叠。本研究还证明,大肠杆菌中重组TTR分子的加工/分泌受到单个氨基酸取代的强烈影响。

相似文献

1
Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP).生产具有生物活性的重组人转甲状腺素蛋白,以了解家族性淀粉样多神经病(FAP)的分子基础。
Biochemistry. 1991 Mar 5;30(9):2415-21. doi: 10.1021/bi00223a017.
2
Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type.葡萄牙型家族性淀粉样多神经病患者血浆转甲状腺素蛋白(前白蛋白)的研究。
J Lab Clin Med. 1983 Oct;102(4):590-603.
3
Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.对患有家族性淀粉样多神经病的葡萄牙患者转甲状腺素蛋白(前白蛋白)基因异常的家族研究。
Ann N Y Acad Sci. 1984;435:86-100. doi: 10.1111/j.1749-6632.1984.tb13742.x.
4
Production and functional analysis of normal and variant recombinant human transthyretin proteins.
J Biol Chem. 1992 Aug 15;267(23):16595-600.
5
Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.在一个希腊裔家族的家族性淀粉样多神经病中存在血浆转甲状腺素蛋白(前白蛋白)变体。
J Lab Clin Med. 1986 Jul;108(1):17-22.
6
Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin.家族性淀粉样多神经病:意大利裔家族中的转甲状腺素蛋白(前白蛋白)变体
Hum Genet. 1988 Dec;80(4):341-3. doi: 10.1007/BF00273648.
7
Comparison of lethal and nonlethal transthyretin variants and their relationship to amyloid disease.致死性和非致死性转甲状腺素蛋白变体的比较及其与淀粉样变性疾病的关系。
Biochemistry. 1995 Oct 17;34(41):13527-36. doi: 10.1021/bi00041a032.
8
Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.葡萄牙家族性淀粉样多神经病患者中异常转甲状腺素蛋白(前白蛋白)的存在。
Trans Assoc Am Physicians. 1983;96:261-70.
9
The Ile-84-->Ser amino acid substitution in transthyretin interferes with the interaction with plasma retinol-binding protein.转甲状腺素蛋白中异亮氨酸84位至丝氨酸的氨基酸替换会干扰其与血浆视黄醇结合蛋白的相互作用。
J Biol Chem. 1994 Sep 23;269(38):23395-8.
10
Interactions amongst plasma retinol-binding protein, transthyretin and their ligands: implications in vitamin A homeostasis and transthyretin amyloidosis.血浆视黄醇结合蛋白、甲状腺素转运蛋白及其配体之间的相互作用:对维生素A稳态和甲状腺素转运蛋白淀粉样变性的影响。
Biochim Biophys Acta. 2004 Dec 1;1703(1):1-9. doi: 10.1016/j.bbapap.2004.09.023.

引用本文的文献

1
In Vitro and In Vivo Effects of SerpinA1 on the Modulation of Transthyretin Proteolysis.丝氨酸蛋白酶抑制剂 A1 对转甲状腺素蛋白蛋白水解的体外和体内调节作用。
Int J Mol Sci. 2021 Aug 31;22(17):9488. doi: 10.3390/ijms22179488.
2
Neuroprotection in early stages of Alzheimer's disease is promoted by transthyretin angiogenic properties.转甲状腺素的血管生成特性可促进阿尔茨海默病早期的神经保护。
Alzheimers Res Ther. 2021 Aug 24;13(1):143. doi: 10.1186/s13195-021-00883-8.
3
The Expression of Chemokines Is Downregulated in a Pre-Clinical Model of TTR V30M Amyloidosis.
在转甲状腺素蛋白 V30M 淀粉样变性的临床前模型中,趋化因子的表达下调。
Front Immunol. 2021 May 19;12:650269. doi: 10.3389/fimmu.2021.650269. eCollection 2021.
4
Preparative Scale Production of Recombinant Human Transthyretin for Biophysical Studies of Protein-Ligand and Protein-Protein Interactions.用于蛋白质-配体和蛋白质-蛋白质相互作用的生物物理研究的重组人转甲状腺素蛋白的制备规模生产。
Int J Mol Sci. 2020 Dec 17;21(24):9640. doi: 10.3390/ijms21249640.
5
Neuronal megalin mediates synaptic plasticity-a novel mechanism underlying intellectual disabilities in megalin gene pathologies.神经元巨蛋白介导突触可塑性——巨蛋白基因病变中智力障碍的一种新机制。
Brain Commun. 2020 Aug 25;2(2):fcaa135. doi: 10.1093/braincomms/fcaa135. eCollection 2020.
6
Repurposing Benzbromarone for Familial Amyloid Polyneuropathy: A New Transthyretin Tetramer Stabilizer.苯溴马隆在家族性淀粉样多发性神经病中的再利用:一种新的转甲状腺素四聚体稳定剂。
Int J Mol Sci. 2020 Sep 28;21(19):7166. doi: 10.3390/ijms21197166.
7
MMP-14 overexpression correlates with the neurodegenerative process in familial amyloidotic polyneuropathy.MMP-14 过表达与家族性淀粉样多发性神经病的神经退行性过程相关。
Dis Model Mech. 2017 Oct 1;10(10):1253-1260. doi: 10.1242/dmm.028571.
8
Cavity filling mutations at the thyroxine-binding site dramatically increase transthyretin stability and prevent its aggregation.甲状腺素结合位点的腔填充突变极大地增加了转甲状腺素蛋白的稳定性并防止其聚集。
Sci Rep. 2017 Mar 24;7:44709. doi: 10.1038/srep44709.
9
A New Folding Kinetic Mechanism for Human Transthyretin and the Influence of the Amyloidogenic V30M Mutation.人转甲状腺素蛋白的一种新的折叠动力学机制及淀粉样变V30M突变的影响
Int J Mol Sci. 2016 Aug 31;17(9):1428. doi: 10.3390/ijms17091428.
10
Resveratrol administration increases Transthyretin protein levels ameliorating AD features- importance of transthyretin tetrameric stability.白藜芦醇给药可提高转甲状腺素蛋白水平,改善阿尔茨海默病特征——转甲状腺素蛋白四聚体稳定性的重要性。
Mol Med. 2016 Oct;22:597-607. doi: 10.2119/molmed.2016.00124. Epub 2016 Jun 30.