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Jaewon Jang

Korea University · 生化学・遺伝学・分子生物学

研究室紹介

Professor Jaewon Jang's research lab specializes in chemical biology and chemical proteomics, focusing on the development of innovative chemical probes and imaging tools to study enzyme activities in living systems. The lab pioneers activity-based protein profiling (ABPP) and radiolabeling strategies to target and visualize serine hydrolases and other post-translationally modified proteins, with applications in cancer biology, neurobiology, and infectious diseases. A central theme is the design of selective, covalent inhibitors and probes that enable dynamic, in vivo functional characterization of enzymes, particularly those involved in metabolic regulation and disease pathogenesis. The lab also develops advanced mass spectrometry and PET imaging techniques to profile labile metabolites and post-translational modifications, such as phosphoaspartate, that are traditionally difficult to capture.

chemical proteomicsactivity-based probesserine hydrolasesPET imagingpost-translational modifications

Research Overview

Papers
154
Total Citations
3,257
Papers (5y)
67
Primary Field
生化学・遺伝学・分子生物学

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
67total
2022
2023
2024
2025
2026
Citations per year (5y)
76total
20222023202420252026

Selected Papers

15
1
Article|192 citations·2012
Highly Selective Inhibitors of Monoacylglycerol Lipase Bearing a Reactive Group that Is Bioisosteric with Endocannabinoid Substrates
Jae Won Chang, Micah J. Niphakis, Kenneth M. Lum, Armand B. Cognetta, Chu Wang, Megan L. Matthews, Sherry Niessen, Matthew W. Buczynski, Loren H. Parsons, Benjamin F. Cravatt
Chemistry & Biology
PharmacologyMedicine
2
Article|135 citations·2013
Proteome-Wide Reactivity Profiling Identifies Diverse Carbamate Chemotypes Tuned for Serine Hydrolase Inhibition
Jae Won Chang, Armand B. Cognetta, Micah J. Niphakis, Benjamin F. Cravatt
SJR Q1ACS Chemical Biology

Serine hydrolases are one of the largest and most diverse enzyme classes in Nature. Inhibitors of serine hydrolases are used to treat many diseases, including obesity, diabetes, cognitive dementia, and bacterial and viral infections. Nonetheless, the majority of the 200+ serine hydrolases in mammals still lack selective inhibitors for their functional characterization. We and others have shown that activated carbamates, through covalent reaction with the conserved serine nucleophile of serine hy

Organic ChemistryChemistry
3
Article|52 citations·2011
An Activity‐Based Imaging Probe for the Integral Membrane Hydrolase KIAA1363
Jae Won Chang, Raymond E. Moellering, Benjamin F. Cravatt
SJR Q1Angewandte Chemie International EditionOA

Profiling enzyme activities: A selective, activity-based imaging probe is described for the integral membrane hydrolase KIAA1363 and used to determine the subcellular localization and half-life of this enzyme in human cancer cells (see picture). Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not respons

PhysiologyBiochemistry, Genetics and Molecular Biology
4
letter|52 citations·2015
Selective Inhibitor of Platelet-Activating Factor Acetylhydrolases 1b2 and 1b3 That Impairs Cancer Cell Survival
Jae Won Chang, Andrea M. Zuhl, Anna E Speers, Sherry Niessen, Steven J Brown, Melinda M. Mulvihill, Yi Fan, Timothy Spicer, Mark R. Southern, Louis Scampavia, Virneliz Fernández-Vega, Melissa M. Dix
SJR Q1ACS Chemical BiologyOA

Platelet-activating factor acetylhydrolases (PAFAHs) 1b2 and 1b3 are poorly characterized serine hydrolases that form a complex with a noncatalytic protein (1b1) to regulate brain development, spermatogenesis, and cancer pathogenesis. Determining physiological substrates and biochemical functions for the PAFAH1b complex would benefit from selective chemical probes that can perturb its activity in living systems. Here, we report a class of tetrahydropyridine reversible inhibitors of PAFAH1b2/3 di

OncologyMedicine
5
Article|24 citations·2018
Chemoproteomic Profiling of Phosphoaspartate Modifications in Prokaryotes
Jae Won Chang, Jeffrey E. Montgomery, Gihoon Lee, Raymond E. Moellering
SJR Q1Angewandte Chemie International Edition

Phosphorylation at aspartic acid residues represents an abundant and critical post-translational modification (PTM) in prokaryotes. In contrast to most characterized PTMs, such as phosphorylation at serine or threonine, the phosphoaspartate moiety is intrinsically labile, and therefore incompatible with common proteomic profiling methods. Herein, we report a nucleophilic, desthiobiotin-containing hydroxylamine (DBHA) chemical probe that covalently labels modified aspartic acid residues in native

SpectroscopyChemistry
6
letter|24 citations·2016
Profiling Reactive Metabolites via Chemical Trapping and Targeted Mass Spectrometry
Jae Won Chang, Gihoon Lee, John S. Coukos, Raymond E. Moellering
SJR Q1Analytical Chemistry

Metabolomic profiling studies aim to provide a comprehensive, quantitative, and dynamic portrait of the endogenous metabolites in a biological system. While contemporary technologies permit routine profiling of many metabolites, intrinsically labile metabolites are often improperly measured or omitted from studies due to unwanted chemical transformations that occur during sample preparation or mass spectrometric analysis. The primary glycolytic metabolite 1,3-bisphosphoglyceric acid (1,3-BPG) ty

Molecular BiologyBiochemistry, Genetics and Molecular Biology
7
Article|22 citations·2020
In Vivo Imaging of the Tumor‐Associated Enzyme NCEH1 with a Covalent PET Probe
Jae Won Chang, Mohammed Bhuiyan, Hsiu‐Ming Tsai, Hannah J. Zhang, Gang Li, Shaghayegh Fathi, David C. McCutcheon, Lara Leoni, R. Freifelder, Chin‐Tu Chen, Raymond E. Moellering
SJR Q1Angewandte Chemie International EditionOA

Abstract Herein, we report the development of an 18 F‐labeled, activity‐based small‐molecule probe targeting the cancer‐associated serine hydrolase NCEH1. We undertook a focused medicinal chemistry campaign to simultaneously preserve potent and specific NCEH1 labeling in live cells and animals, while permitting facile 18 F radionuclide incorporation required for PET imaging. The resulting molecule, [ 18 F]JW199, labels active NCEH1 in live cells at nanomolar concentrations and greater than 1000‐

Molecular BiologyBiochemistry, Genetics and Molecular Biology
8
Article|14 citations·2011
An Activity‐Based Imaging Probe for the Integral Membrane Hydrolase KIAA1363
Jae Won Chang, Raymond E. Moellering, Benjamin F. Cravatt
Angewandte Chemie

Enzymaktivitäten: Eine selektive, aktivitätsbasierte Sonde, die das integrale Membranhydrolase-Enzym KIAA1363 abbilden kann, wird beschrieben und zur subzellulären Lokalisation sowie zur Bestimmung der Halbwertszeit des Enzyms in Krebszellen verwendet (siehe Bild).

Molecular BiologyBiochemistry, Genetics and Molecular Biology
9
Article|9 citations·2024
Development of a Dual‐Factor Activatable Covalent Targeted Photoacoustic Imaging Probe for Tumor Imaging
Jiho Song, Tianqu Zhai, Heung Sik Hahm, Yuancheng Li, Hui Mao, Xueding Wang, Janggun Jo, Janggun Jo, Jae Won Chang
SJR Q1Angewandte Chemie International Edition

Photoacoustic imaging (PAI) is an emerging modality in biomedical imaging with superior imaging depth and specificity. However, PAI still has significant limitations, such as the background noise from endogenous chromophores. To overcome these limitations, we developed a covalent activity-based PAI probe, NOx-JS013, targeting NCEH1. NCEH1, a highly expressed and activated serine hydrolase in aggressive cancers, has the potential to be employed for the diagnosis of cancers. We show that NOx-JS013

Biomedical EngineeringEngineering
10
letter|8 citations·2019
No Bones About It: Small Molecules for Bone Regeneration
Jae Won Chang, Raymond E. Moellering
SJR Q1Cell chemical biologyOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
11
Article|7 citations·2006
Lateral force microscopy of bamboo-shaped multiwalled carbon nanotubes
장재원, 이철의, 이태재, 류승철, 이철진

Morphologies of bamboo-shaped multiwalled carbon nanotubes (BS-MWNTs) grown on Fe catalyst deposited onto SiO2/Tisubstrates by thermal chemical vapor deposition were investigated by means of atomic force microscopy (AFM) and lateral forcemicroscopy (LFM). For the structural speciality, the bamboo structures were more distinctly observed by LFM

12
Article|6 citations·2003
Structure and morphology of vacuum-evaporated pentacene as a function of the substrate temperature
Jae Won Chang, Hoon Kim, Jai Kyeong Kim, Byeong‐Kwon Ju, Jin Jang, Yun Hi Lee
SJR Q3Journal of the Korean Physical Society
Materials ChemistryMaterials Science
13
Article|3 citations·2019
페드로 알모도바르의 를 통해 본 주체의 문제
장재원, 김유진

The current study investigates the problems of subject observed in The Skin I Live In, directed by Pedro Almodovar in 2011. One of the oldest philosophical questions held by people is: “Who am I?” or “What is the essence of humanity?” Breaking away from traditional Western philosophy that identified humans as rational beings, the contemporary philosophy since the advent of phenomenology views humans as beings of corporeal and generative beings. Among such discourse about the corporeal taking pla

14
Article|2 citations·2022
스페인 중세 시 『죽음의 무도』에 드러난 사회 비판 연구
장재원

The purpose of this study is to analyze the change in social consciousness after the outbreak of the Black Death, which was revealed in the late medieval Spanish poem Danza General de la muerte, and to reflect on its significance. As is well known, the Black Death Pandemic sacrificed nearly a third of Europe's population between 1347 and 1351, and was taken a significant opportunity to accelerate the transition from the Middle Ages to the Renaissance. Danza de la muerte as new motif in literatur

15
Article|2 citations·2018
Chemoproteomic Profiling of Phosphoaspartate Modifications in Prokaryotes
Jae Won Chang, Jeffrey E. Montgomery, Gihoon Lee, Raymond E. Moellering
Angewandte Chemie

Abstract Phosphorylation at aspartic acid residues represents an abundant and critical post‐translational modification (PTM) in prokaryotes. In contrast to most characterized PTMs, such as phosphorylation at serine or threonine, the phosphoaspartate moiety is intrinsically labile, and therefore incompatible with common proteomic profiling methods. Herein, we report a nucleophilic, desthiobiotin‐containing hydroxylamine (DBHA) chemical probe that covalently labels modified aspartic acid residues

SpectroscopyChemistry

Research Areas

Cancer ResearchMolecular BiologyPulmonary and Respiratory MedicineOrganic ChemistryPharmacologyLiterature and Literary Theory

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