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The peptide literature, summarized and graded.

Every paper distilled to a plain-language summary with an honest evidence grade — from strong human trials to animal-only signals. 2 papers indexed and counting.

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Filtered by #GHRP-2 · clear
Limited · humanPreprint

Unveiling the Role of Melatonin in Coronary Heart Disease: Identification and Experimental Validation of Novel Biomarkers

This bioinformatics study investigated the role of melatonin-related genes in coronary heart disease (CHD) by analyzing two publicly available gene expression datasets (GSE179789 and GSE113079). Using differential expression analysis and validation, the researchers identified two genes—MAP2K2 (a mitogen-activated protein kinase kinase) and PGD (phosphogluconate dehydrogenase)—as candidate CHD biomarkers, both showing significant upregulation in CHD samples across both datasets. Gene set enrichment analysis (GSEA) linked these genes to pathways including ribosome function, prion diseases, and Parkinson's disease. The study also mapped complex regulatory networks involving lncRNAs, miRNAs, and transcription factors; notably, four lncRNAs (NEAT1, AP000766.1, LINC02381, and XIST) were found to regulate PGD via hsa-let-7e-5p, and 29 transcription factors co-regulated both biomarkers. Drug-target network analysis predicted 41 drugs targeting MAP2K2 and 3 targeting PGD. Biomarker expression was further validated in clinical samples via RT-qPCR. Limitations include the observational and computational nature of the study, reliance on public datasets, small clinical validation cohorts typical of such designs, and the absence of functional or mechanistic experiments confirming causal roles. The study is reported as a preprint and has not undergone formal peer review.

Unknown journal · Apr 2026DOI ↗
Limited · human

Simplifying and expanding the screening for peptides <2 kDa by direct urine injection, liquid chromatography, and ion mobility mass spectrometry.

This study developed and validated an analytical method for detecting a broad panel of 18 performance-enhancing peptides (molecular weight <2 kDa) in human urine, as defined by the World Anti-Doping Agency (WADA) prohibited list. The method uses direct urine injection—bypassing complex sample preparation—coupled with liquid chromatography and ion mobility time-of-flight mass spectrometry (IM-TOFMS). The researchers reported limits of detection (LOD) ranging from 50 to 500 pg/mL, well below WADA's minimum required performance level of 2 ng/mL. The method demonstrated acceptable precision (imprecision <20%) and linearity across a 0–10 ng/mL working range. Stability testing identified –20°C as the appropriate storage temperature for urine samples. As a proof-of-concept, the method was applied to real elimination study urine samples from individuals who had administered GHRP-2, GHRP-6, or LHRH, successfully detecting these compounds. Key limitations include the small number of human subjects used in the elimination studies, which were primarily intended to demonstrate analytical feasibility rather than investigate pharmacokinetics or clinical effects. The study is a methodological/analytical validation paper focused on anti-doping screening, not a clinical or therapeutic investigation.

Journal of separation science · Dec 2015DOI ↗