Transcription-Translation Coupling in bacteria
I study how RNA polymerase and ribosomes stay coordinated during gene expression.
Damon Runyon Postdoctoral Fellow · MIT
I am a systems biologist who studies how bacteria coordinate transcription, translation, and RNA decay to achieve precise gene expression.
I am a Damon Runyon Postdoctoral Fellow in the Gene-Wei Li lab at MIT Biology and HHMI. I study bacterial gene expression using systems level approaches, with a focus on how bacteria coordinate transcription, translation, and RNA decay to achieve precise control of gene expression.
For my postdoctoral work, I use system wide measurements and computational analysis to address these questions. During my PhD, I trained in biochemistry and structural biology and used in vitro assays and cryo-EM to study how bacterial RNA polymerase pauses, terminates, and responds to regulatory proteins during transcription.
Each of these projects is described in detail in the Research section.
I study how RNA polymerase and ribosomes stay coordinated during gene expression.
This project showed how NusG stabilizes a paused RNA polymerase in Mycobacterium tuberculosis. Study was published in Molecular Cell (2023) .
This project revealed the first atomic structures that show, step by step, how intrinsic termination occurs in bacteria. Results were reported in Nature (2023) .
Monitored the folding and nucleation kinetics of denatured amyloid-β monomers using cysteine-mediated quenching of tryptophan autofluorescence.
April 2025
Received the Outstanding Alumni Award from the Charles Drew Science Program at Michigan State University.
May 2024
Awarded the Damon Runyon Postdoctoral Fellowship.
November 2023
PhD thesis published in ProQuest.
July 2023
Won Best Poster Presentation at the Tuberculosis Drug Discovery and Development GRC in Barcelona.
April 2023
Mechanism of NusG regulated transcription elongation published in Molecular Cell.
Download a full summary of my training research experience and publications.
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