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兔对 NOTCH3 肽免疫原 C 末端的优先抗体反应。

Preferential rabbit antibody responses to C-termini of NOTCH3 peptide immunogens.

机构信息

Department of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.

Neurology Service, Department of Veterans Affairs, VA Ann Arbor Healthcare System, Ann Arbor, MI, 48105, USA.

出版信息

Sci Rep. 2023 Jun 6;13(1):9156. doi: 10.1038/s41598-023-36067-7.

DOI:10.1038/s41598-023-36067-7
PMID:37280231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10244458/
Abstract

Antibodies raised in peptide-immunized rabbits have been used in biological research for decades. Although there has been wide implementation of this approach, specific proteins are occasionally difficult to target for multiple reasons. One consideration that was noted in mice is that humoral responses may preferentially target the carboxyl terminus of the peptide sequence which is not present in the intact protein. To shed light on the frequency of preferential rabbit antibody responses to C-termini of peptide immunogens, we present our experience with generation of rabbit antibodies to human NOTCH3. A total of 23 antibodies were raised against 10 peptide sequences of human NOTCH3. Over 70% (16 of 23) of these polyclonal antibodies were determined to be C-terminal preferring: NOTCH3 peptide-reactive antibodies largely targeted the terminating free carboxyl group of the immunizing peptide. The antibodies that preferred C-terminal epitopes reacted weakly or not at all with recombinant target sequences with extension the C-terminus that eliminated the free carboxyl group of the immunogen structure; furthermore, each of these antisera revealed no antibody reactivity to proteins truncated before the C-terminus of the immunogen. In immunocytochemical applications of these anti-peptide antibodies, we similarly found reactivity to recombinant targets that best binding to cells expressing the free C-terminus of the immunizing sequence. In aggregate, our experience demonstrates a strong propensity for rabbits to mount antibody responses to C-terminal epitopes of NOTCH3-derived peptides which is predicted to limit their use against the native protein. We discuss some potential approaches to overcome this bias that could improve the efficiency of generation of antibodies in this commonly utilized experimental paradigm.

摘要

几十年来,在肽免疫兔中产生的抗体已被用于生物研究。尽管这种方法已经得到了广泛的应用,但由于多种原因,特定的蛋白质偶尔难以成为靶标。在小鼠中注意到的一个考虑因素是,体液免疫反应可能优先针对肽序列的羧基末端,而该末端在完整蛋白质中不存在。为了阐明针对肽免疫原 C 末端的兔抗体优先反应的频率,我们介绍了我们生成针对人 NOTCH3 的兔抗体的经验。总共针对人 NOTCH3 的 10 个肽序列产生了 23 种抗体。这些多克隆抗体中超过 70%(23 种中的 16 种)被确定为 C 末端优先:NOTCH3 肽反应性抗体主要针对免疫肽的终止游离羧基基团。优先针对 C 末端表位的抗体与延伸 C 末端消除免疫原结构游离羧基基团的重组靶序列的反应较弱或根本没有反应;此外,这些抗血清中的每一种都没有针对免疫原 C 末端之前截断的蛋白质的抗体反应性。在这些抗肽抗体的免疫细胞化学应用中,我们同样发现它们与最好与表达免疫序列游离 C 末端的细胞结合的重组靶标具有反应性。总之,我们的经验表明,兔对 NOTCH3 衍生肽的 C 末端表位产生抗体反应的强烈倾向,这预计会限制它们在天然蛋白中的应用。我们讨论了一些潜在的方法来克服这种偏见,这可能会提高在这种常用实验范例中生成抗体的效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/70e4d154aa5b/41598_2023_36067_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/4bc0becb217a/41598_2023_36067_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/74f4f2e80acb/41598_2023_36067_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/d5b884798285/41598_2023_36067_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/b67fd8f4e974/41598_2023_36067_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/70e4d154aa5b/41598_2023_36067_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/4bc0becb217a/41598_2023_36067_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/74f4f2e80acb/41598_2023_36067_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/d5b884798285/41598_2023_36067_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/b67fd8f4e974/41598_2023_36067_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85c7/10244458/70e4d154aa5b/41598_2023_36067_Fig5_HTML.jpg

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本文引用的文献

1
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Int J Mol Sci. 2022 Mar 27;23(7):3671. doi: 10.3390/ijms23073671.
2
Hydrolysis of a second Asp-Pro site at the N-terminus of NOTCH3 in inherited vascular dementia.遗传性血管性痴呆中 NOTCH3 N 端第 2 个 Asp-Pro 位点的水解。
Sci Rep. 2021 Aug 26;11(1):17246. doi: 10.1038/s41598-021-96679-9.
3
Context-dependent monoclonal antibodies against protein carbamidomethyl-cysteine.针对蛋白质半胱氨酸甲酰化的上下文相关单克隆抗体。
PLoS One. 2020 Nov 24;15(11):e0242376. doi: 10.1371/journal.pone.0242376. eCollection 2020.
4
Binding of omeprazole to protein targets identified by monoclonal antibodies.奥美拉唑结合蛋白靶标的单克隆抗体鉴定。
PLoS One. 2020 Sep 18;15(9):e0239464. doi: 10.1371/journal.pone.0239464. eCollection 2020.
5
NOTCH3 is non-enzymatically fragmented in inherited cerebral small-vessel disease.NOTCH3 在遗传性脑小血管病中非酶切片段化。
J Biol Chem. 2020 Feb 14;295(7):1960-1972. doi: 10.1074/jbc.RA119.007724. Epub 2020 Jan 4.
6
Peptides, Antibodies, Peptide Antibodies and More.肽、抗体、肽抗体及更多。
Int J Mol Sci. 2019 Dec 13;20(24):6289. doi: 10.3390/ijms20246289.
7
CADASIL.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病
Handb Clin Neurol. 2018;148:733-743. doi: 10.1016/B978-0-444-64076-5.00047-8.
8
Blood biomarkers in a mouse model of CADASIL.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)小鼠模型中的血液生物标志物
Brain Res. 2016 Aug 1;1644:118-26. doi: 10.1016/j.brainres.2016.05.008. Epub 2016 May 10.
9
Latent NOTCH3 epitopes unmasked in CADASIL and regulated by protein redox state.潜在的NOTCH3表位在CADASIL中暴露,并受蛋白质氧化还原状态调控。
Brain Res. 2014 Oct 2;1583:230-6. doi: 10.1016/j.brainres.2014.08.018. Epub 2014 Aug 21.
10
Generation and characterization of antibodies specific for caspase-cleaved neo-epitopes: a novel approach.针对半胱氨酸天冬氨酸蛋白酶切割的新表位的抗体的产生和鉴定:一种新方法。
Cell Death Dis. 2011 Sep 1;2(9):e205. doi: 10.1038/cddis.2011.91.