Evidence map›Paper›PMID 36076853›Full record

ArticleFoods (Basel, Switzerland)2022

Preparation, Characterization and In Vitro Stability of a Novel ACE-Inhibitory Peptide from Soybean Protein.

Sara Sangiorgio, Nikolina Vidović, Giovanna Boschin, Gilda Aiello, Patrizia Arcidiaco, Anna Arnoldi, Carlo F Morelli, Marco Rabuffetti, Teresa Recca, Letizia Scarabattoli and 2 more

Abstract read
In one paragraph

Article in Foods (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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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

12 authors.

Sara SangiorgioDepartment of Chemistry, University of Milan, Golgi 19, 20133 Milan, Italy.
Nikolina VidovićDepartment of Chemistry, University of Milan, Golgi 19, 20133 Milan, Italy.ORCID 0000-0003-0710-143X
Giovanna BoschinDepartment of Pharmaceutical Sciences, University of Milan, L. Mangiagalli 25, 20133 Milan, Italy.ORCID 0000-0003-4949-2061
Gilda AielloDepartment of Pharmaceutical Sciences, University of Milan, L. Mangiagalli 25, 20133 Milan, Italy.ORCID 0000-0003-4327-0521
Patrizia ArcidiacoCentro Grandi Strumenti, University of Pavia, Bassi 21, 27100 Pavia, Italy.ORCID 0000-0002-1369-5011
Anna ArnoldiDepartment of Pharmaceutical Sciences, University of Milan, L. Mangiagalli 25, 20133 Milan, Italy.ORCID 0000-0002-0987-3014
Carlo F MorelliDepartment of Chemistry, University of Milan, Golgi 19, 20133 Milan, Italy.ORCID 0000-0001-6314-6902
Marco RabuffettiDepartment of Chemistry, University of Milan, Golgi 19, 20133 Milan, Italy.ORCID 0000-0003-2089-1333
Teresa ReccaCentro Grandi Strumenti, University of Pavia, Bassi 21, 27100 Pavia, Italy.ORCID 0000-0002-2000-7846
Letizia ScarabattoliDepartment of Chemistry, University of Milan, Golgi 19, 20133 Milan, Italy.ORCID 0000-0002-6360-0893
Daniela UbialiDepartment of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.ORCID 0000-0003-3528-2960
Giovanna SperanzaDepartment of Chemistry, University of Milan, Golgi 19, 20133 Milan, Italy.ORCID 0000-0003-4544-1515

Funding

Fondazione Cariplo project BIOCOSM, ID 2017-0978
6 · The paper itself

Abstract

A soy protein isolate was hydrolyzed with Alcalase®, Flavourzyme® and their combination, and the resulting hydrolysates (A, F and A + F) were ultrafiltered and analyzed through SDS-PAGE. Fractions with MW < 1 kDa were investigated for their ACE-inhibitory activity, and the most active one (A < 1 kDa) was purified by semi-preparative RP-HPLC, affording three further subfractions. NMR analysis and Edman degradation of the most active subfraction (A1) enabled the identification of four putative sequences (ALKPDNR, VVPD, NDRP and NDTP), which were prepared by solid-phase synthesis. The comparison of their ACE-inhibitory activities suggested that the novel peptide NDRP might be the main agent responsible for A1 fraction ACE inhibition (ACE inhibition = 87.75 ± 0.61%; IC50 = 148.28 ± 9.83 μg mL−1). NDRP acts as a non-competitive inhibitor and is stable towards gastrointestinal simulated digestion. The Multiple Reaction Monitoring (MRM) analysis confirmed the presence of NDRP in A < 1 kDa.

Indexed as

ACE inhibitorfunctional foodLineweaver–Burk plotpeptide synthesissimulated gastrointestinal digestionsoybean protein hydrolysate

Identifiers

PMID36076853
PMCPMC9455805

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Registered trials

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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.