June 12, 2026 Review
Endolysins from Cutibacterium acnes phages as alternative antibiotics
NATPRO J (2026) 3: 23-26
https://doi.org/10.23177/NJ026.0402
Authors: Muhammad Adeel Hasnain and Gi-Seong Moon*
Abstract: The rising antibiotic resistance of Cutibacterium acnes and the disruption of the skin microbiome have necessitated the development of alternative acne therapies. Bacteriophage-derived endolysins have emerged as a promising, microbiome-friendly antimicrobial strategy. These enzymes rapidly and specifically degrade the bacterial cell wall, selectively targeting pathogens without harming beneficial microbiota. Furthermore, endolysins exhibit a low propensity for resistance development and are highly effective against biofilms. Recent advancements in protein engineering—focusing on the enzymatic active domain (EAD) and cell wall-binding domain (CBD)—have enabled the structural optimization of recombinant endolysins for enhanced therapeutic efficacy. This paper outlines the mechanism of action, technological developments, and patent trends of C. acnes-targeting endolysins, highlighting their significant clinical and commercial potential as next-generation targeted topical therapeutics in dermatological care.
Received: April 3, 2026; Revised: May 26, 2026; Accepted: June 11, 2026; Published: June 12, 2026; E-mail: gsmoon@ut.ac.kr
June 8, 2026 Review
Peptidomics and Mass Spectrometry: Enabling the Discovery of Short Peptides as Novel Natural Products
NATPRO J (2026) 3: 17-22
https://doi.org/10.23177/NJ026.0407
Authors: Jong Suk Lee* and Jun Ho Shin
Abstract: Food proteins are routinely exposed to gastrointestinal proteolysis, generating complex peptide mixtures that include both transient intermediates and biologically active sequences. While the nutritional role of proteins has long been recognized, the diversity and biological activity of peptides generated during digestion have remained largely unexplored due to analytical limitations. Recent advances in high-resolution mass spectrometry and peptidomics have made it possible to profile hydrolysis-derived peptides at scale with substantially improved depth and confidence. Short peptides represent a chemically diverse molecular space with potential applications as bioactive compounds. The theoretical diversity of peptide sequences increases exponentially (20ⁿ, where n = peptide length), far exceeding the structural space explored by conventional natural product discovery methods. Furthermore, peptides derived from dietary proteins are expected to exhibit favorable safety profiles due to their long history of human consumption. This perspective highlights the emerging paradigm of short peptide discovery through mass-spectrometry-based peptidomics and discusses its technological, industrial, and market implications for functional foods, pharmaceuticals, and cosmetic applications.
Received: May 1, 2026; Revised: June 5, 2026; Accepted: June 5, 2026; Published: June 8, 2026; E-mail: leejs@gbsa.or.kr
May 7, 2026 Article
HPLC Quantification and In Silico Analysis of Polyphenols from Moringa oleifera Targeting FPR2 in Epithelial Ovarian Cancer
NATPRO J (2026) 3: 9-16
https://doi.org/10.23177/NJ026.0404
Authors: Chang-Dae Lee1 and Sanghyun Lee1,2*
Abstract: This study investigated the polyphenolic composition of Moringa oleifera and evaluated its potential biological relevance for epithelial ovarian cancer (EOC) using an integrated analytical and computational approach. High-performance liquid chromatography (HPLC) analysis revealed that (+)-catechin and quercetin 3-glucuronide were the major compounds, with concentrations of 32.12 mg/g and 19.14 mg/g, respectively. Network pharmacology and molecular docking were employed to predict the molecular targets and elucidate the pharmacological mechanisms of these compounds in the context of EOC. The results suggested that these compounds may interact with formyl peptide receptor 2 (FPR2), a key receptor highly implicated in EOC pathogenesis and inflammation-related signaling pathways. Both (+)-catechin and quercetin 3-glucuronide exhibited strong binding affinities to FPR2 in docking simulations, with scores of –8.7 and –10.7 kcal/mol, respectively, indicating possible involvement in modulating FPR2-related biological processes in EOC. These findings provide basic information on the polyphenolic profile of M. oleifera and suggest its potential as a source of bioactive compounds with potential applications to EOC-related biological processes. However, further experimental studies are required to validate these observations.
Received: April 6, 2026; Revised: April 30, 2026; Accepted: May 6, 2026; Published: May 7, 2026; E-mail: slee@cau.ac.kr
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