Cangming Yang , Zachary Z. Brown , Tao Meng , John R. Frost , Ashwin Rao , Xiaohong Zhu , Natalya Pissarnitski , Tianying Jian , Jianping Pan , Min Liu
{"title":"在发现化学中实现更快、更环保的肽纯化","authors":"Cangming Yang , Zachary Z. Brown , Tao Meng , John R. Frost , Ashwin Rao , Xiaohong Zhu , Natalya Pissarnitski , Tianying Jian , Jianping Pan , Min Liu","doi":"10.1016/j.jchromb.2025.124795","DOIUrl":null,"url":null,"abstract":"<div><div>Peptides are attracting broad interest across the pharmaceutical industry owing to their vast therapeutic potential for drugging high-value targets and flexible dosing and formulation options to improve patient access. As the industry increases focus on peptide-based discovery programs, fast, high-throughput, and green purification methods have become increasingly valuable. Due to the vast sequence and physicochemical diversity of peptides, expedited purification of large libraries has remained a challenge. Herein, we describe the development of a High-Throughput Purification (HTP) approach for peptides wherein each purification is achieved in 6 min or less, representing a substantial reduction in time and solvent consumption compared with conventional methods, all while maintaining high purity levels. This approach relies on Reversed-Phase High-Performance Liquid Chromatography (RP-HPLC), leveraging a dual pump preparative system and short focused solvent gradients to reduce purification times and achieve highly efficient and accelerated high-throughput purification.</div></div>","PeriodicalId":348,"journal":{"name":"Journal of Chromatography B","volume":"1267 ","pages":"Article 124795"},"PeriodicalIF":2.8000,"publicationDate":"2025-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enabling faster and greener peptide purification in discovery chemistry\",\"authors\":\"Cangming Yang , Zachary Z. Brown , Tao Meng , John R. Frost , Ashwin Rao , Xiaohong Zhu , Natalya Pissarnitski , Tianying Jian , Jianping Pan , Min Liu\",\"doi\":\"10.1016/j.jchromb.2025.124795\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Peptides are attracting broad interest across the pharmaceutical industry owing to their vast therapeutic potential for drugging high-value targets and flexible dosing and formulation options to improve patient access. As the industry increases focus on peptide-based discovery programs, fast, high-throughput, and green purification methods have become increasingly valuable. Due to the vast sequence and physicochemical diversity of peptides, expedited purification of large libraries has remained a challenge. Herein, we describe the development of a High-Throughput Purification (HTP) approach for peptides wherein each purification is achieved in 6 min or less, representing a substantial reduction in time and solvent consumption compared with conventional methods, all while maintaining high purity levels. This approach relies on Reversed-Phase High-Performance Liquid Chromatography (RP-HPLC), leveraging a dual pump preparative system and short focused solvent gradients to reduce purification times and achieve highly efficient and accelerated high-throughput purification.</div></div>\",\"PeriodicalId\":348,\"journal\":{\"name\":\"Journal of Chromatography B\",\"volume\":\"1267 \",\"pages\":\"Article 124795\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chromatography B\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1570023225003496\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chromatography B","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1570023225003496","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Enabling faster and greener peptide purification in discovery chemistry
Peptides are attracting broad interest across the pharmaceutical industry owing to their vast therapeutic potential for drugging high-value targets and flexible dosing and formulation options to improve patient access. As the industry increases focus on peptide-based discovery programs, fast, high-throughput, and green purification methods have become increasingly valuable. Due to the vast sequence and physicochemical diversity of peptides, expedited purification of large libraries has remained a challenge. Herein, we describe the development of a High-Throughput Purification (HTP) approach for peptides wherein each purification is achieved in 6 min or less, representing a substantial reduction in time and solvent consumption compared with conventional methods, all while maintaining high purity levels. This approach relies on Reversed-Phase High-Performance Liquid Chromatography (RP-HPLC), leveraging a dual pump preparative system and short focused solvent gradients to reduce purification times and achieve highly efficient and accelerated high-throughput purification.
期刊介绍:
The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis.
Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches.
Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.