Author

Matthew Chang

Cornell UniversityPrimary ORCID profile (0000-0002-9486-1228 · 2 papers)Unclaimed ORCID profile · follow to get notified of new preprints

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Same name, identified by ORCID

Matthew ChangiD2 papers · Memorial Sloan Kettering Cancer Center

Biology Disciplines

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Cell Biology· 1 Synthetic Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Organism:E. coli· 1 Organism:human· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

Abhijit ParoliaiD· 1 shared Andrew D. PattersoniD· 1 shared Benjamin S. HalliganiD· 1 shared Brandon CheniD· 1 shared Costas A. LyssiotisiD· 1 shared David A. HannaiD· 1 shared David J. PagliariniiD· 1 shared Drew C. StarkiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperCell Biology

Abhijit ParoliaORCID

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Author profile →

2 papers

Recent·Most cited

BRD4-mediated epigenetic regulation of endoplasmic reticulum-mitochondria contact sites is governed by the mitochondrial complex III

Brandon Chen, Drew C. Stark, Pankaj V. Jadhav, Theophilus M. Lynn-Nguyen, Benjamin S. Halligan, Nicholas J. Rossiter, Nicole Sindoni, Myunsun Shin, Joao A. Paulo, Matthew Chang, Imhoi Koo, Sergei Koshkin, Sanjana Eyunni, Paolo Ronchi, Michelle T. Paulsen, , Yatrik M. Shah

The paper identifies fedratinib as a drug that increases endoplasmic reticulum-mitochondria contact sites by inhibiting BRD4, revealing a novel epigenetic pathway linking ERMCS to cellular metabolism.

bioRxiv · Feb 2, 2024 · PreprintCell Biology

Isolation of full-length IgG antibodies from combinatorial libraries expressed in the cytoplasm of Escherichia coli

Michael-Paul Robinson, Jinjoo Jung, Natalia Lopez‐Barbosa, Matthew Chang, Mingji Li, Thapakorn Jaroentomeechai, Emily C. Cox, Xiaolu Zheng, Mehmet Berkmen, Matthew P. DeLisa

The paper describes a method to isolate full-length IgG antibodies from combinatorial libraries in E. coli using a bifunctional antigen substrate for selection.

Nature Communications · Jun 14, 2023Peer-reviewedSynthetic Biology