Evidence map›Paper›PMID 42213345›Full record

ArticleThe protein journal2026

Screening of Small Peptide Against Ischemic Fatty-Acid Binding Protein (FABP).

Harshita Shand, Soumendu Patra, Thirumurthy Madhavan, Suvankar Ghorai

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Article in The protein journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Harshita ShandInfection and Disease Biology Laboratory, Department of Microbiology, Raiganj University, North Dinajpur, West Bengal, 733134, India.
Soumendu PatraInfection and Disease Biology Laboratory, Department of Microbiology, Raiganj University, North Dinajpur, West Bengal, 733134, India.
Thirumurthy MadhavanComputational Biology Laboratory, Department of Genetic Engineering, School of Bioengineering, SRM Institute of Science and Technology, Chengalpattu District, Kattankulathur, Potheri, Tamilnadu, 603203, India.
Suvankar GhoraiInfection and Disease Biology Laboratory, Department of Microbiology, Raiganj University, North Dinajpur, West Bengal, 733134, India. suvankarbt@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A low-molecular-weight cytoplasmic protein called heart-type fatty acid-binding protein (H-FABP) is released by cardiac myocytes during an ischemic episode. The normal serum level of FABP is around 3.5 ± 0.4 ng/ml (males), 3.9 ± 0.4 ng/ml (females), while the cutoff value of H-FABP in case of acute myocardial infarction (AMI) is 21.85 ng/ml within 3 hours. In case of angina pectoris, ischemic patients can be distinguished from non-ischemic patients and treated appropriately by detecting the presence of serum H-FABP in a point-of-care (POC) diagnostic approach. As the mortality rate due to coronary heart disease is on the rise worldwide, serum H-FABP levels can act as a diagnostic marker to assist in the prediction of probable cardiac arrest. In the present work, a small peptide against H-FABP has been screened by phage DNA library screening, which can be used for the development of a rapid and accurate diagnostic system for serum H-FABP. The cloning, expression and purification of the H-FABP protein in bacteria and screening of a 12 amino-acid long screened peptide with moderate affinity for binding to H-FABP is reported. The interaction of the said peptide with H-FABP was confirmed by in-silico methods like molecular docking and molecular dynamics simulation. The affinity of the peptide binding to H-FABP was assessed using Isothermal Titration Calorimetry (ITC). A spontaneous process is indicated by ΔG (-7.98 kcal mol

Indexed as

Fatty Acid-Binding ProteinsPeptidesAmino Acid SequenceFatty Acid Binding Protein 3HumansMolecular Docking SimulationPeptide LibraryProtein BindingFABP3 protein, humanFatty Acid Binding Protein 3Fatty Acid-Binding ProteinsPeptide LibraryPeptidesH-FABPITCMolecular docking-simulationPeptidePhage DNA library screening

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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.