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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.

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/85c7/10244458/4bc0becb217a/41598_2023_36067_Fig1_HTML.jpg

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