Evidence map›Paper›PMID 37280231›Full record

ArticleScientific reports2023

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

Soo Jung Lee, Mitchell B Gasche, Connor J Burrows, Akhil Kondepudi, Xiaojie Zhang, Michael M Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 82% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Soo Jung LeeDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
Mitchell B GascheDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
Connor J BurrowsDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
Akhil KondepudiDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
Xiaojie ZhangDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
Michael M WangDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA. micwang@umich.edu.
University of Michigan · US

Funding

NOTCH3 N-terminal fragmentation in cerebral small vessel diseaseR01NS099160 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, MICHAEL M · 2018 to 2022
$1.6M
Pathological protein generation in cerebral small vessel diseaseI01BX003824 · VA · VETERANS HEALTH ADMINISTRATION · PI Michael M Wang · 2017 to 2026
–
Transformation of NOTCH3 protein in cerebral small vessel diseaseI01BX003855 · VA · VETERANS HEALTH ADMINISTRATION · PI WANG, MICHAEL M · 2018 to 2021
–
BLRD VA I01 BX003824BLRD VA I01 BX003855NINDS NIH HHS R01 NS099160
6 · The paper itself

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.

Indexed as

Antibody FormationPeptidesAmino Acid SequenceAnimalsAntibodiesAntigensEpitopesHumansMicePeptide FragmentsProteinsRabbitsReceptor, Notch3AntibodiesAntigensEpitopesNOTCH3 protein, humanPeptide FragmentsPeptidesProteinsReceptor, Notch3

Identifiers

PMID37280231
PMCPMC10244458
OpenAlexW4379536951

What OpenQuestion holds

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.