
Philip Bevilacqua
· Co-Director, Center for RNA Molecular Biology; Distinguished Professor of Chemistry and of Biochemistry and Molecular BiologyPennsylvania State University · Biochemistry and Molecular Biology
Active 1989–2026
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About
Philip Bevilacqua is a Distinguished Professor of Chemistry and Biochemistry and Molecular Biology at Penn State University, where he also serves as Co-Director of the Center for RNA Molecular Biology. His research focuses on RNA folding in vivo and genome-wide, RNA regulation of gene expression, ribozyme mechanisms, and the roles RNA may have played in the emergence of life on early Earth. Bevilacqua's work involves developing methods to identify and characterize modifications to RNA structure that can alter its function and serve as potential drug targets. His contributions include advancing understanding of RNA structure probing, RNA thermometers that regulate translation, and the molecular principles underlying RNA's versatility and functionality.
Research topics
- Biology
- Chemistry
- Biochemistry
- Biophysics
- Cell biology
- Genetics
- Organic chemistry
- Molecular biology
- Chromatography
- Ecology
Selected publications
Nature Communications · 2020 · 179 citations
Multivalent polyions can undergo complex coacervation, producing membraneless compartments that accumulate ribozymes and enhance catalysis, and offering a mechanism for functional prebiotic compartmentalization in the origins of life. Here, we evaluate the impact of lower, more prebiotically-relevant, polyion multivalency on the functional performance of coacervates as compartments. Positively and negatively charged homopeptides with 1-100 residues and adenosine mono-, di-, and triphosphate nucl…
Nature Chemistry · 2022 · 150 citations
RNA multimerization as an organizing force for liquid–liquid phase separation
RNA · 2021 · 60 citations
1st authorCorrespondingRNA interactions are exceptionally strong and highly redundant. As such, nearly any two RNAs have the potential to interact with one another over relatively short stretches, especially at high RNA concentrations. This is especially true for pairs of RNAs that do not form strong self-structure. Such phenomena can drive liquid-liquid phase separation, either solely from RNA-RNA interactions in the presence of divalent or organic cations, or in concert with proteins. RNA interactions can drive mult…
Tissue-specific changes in the RNA structurome mediate salinity response in <i>Arabidopsis</i>
RNA · 2020 · 38 citations
under salinity stress, which negatively impacts agriculture. Structure-seq utilizes dimethyl sulfate reactivity to identify As and Cs that lack base-pairing or protection. Salt stress refolded transcripts differentially in root versus shoot, evincing tissue specificity of the structurome. Both tissues exhibited an inverse correlation between salt stress-induced changes in transcript reactivity and changes in abundance, with stress-related mRNAs showing particular structural dynamism. This invers…
CsrA-Mediated Translational Activation of <i>ymdA</i> Expression in Escherichia coli
mBio · 2020 · 32 citations
mRNA activates translation by destabilizing a structure that otherwise prevents ribosome binding. The extensive role of CsrA in activating gene expression suggests the common occurrence of similar activation mechanisms.
Recent grants
NSF · $1.8M · 2021–2026
Mechanistic studies of proton transfer in ribozyme self-cleavage
NSF · $356k · 2012–2017
NIH · $3.0M · 2013
Frequent coauthors
- 42 shared
Sarah M. Assmann
Pennsylvania State University
- 41 shared
David J. Proctor
- 30 shared
Ryszard Kierzek
Institute of Bioorganic Chemistry, Polish Academy of Sciences
- 26 shared
Joshua M. Blose
- 23 shared
Barbara L. Golden
Purdue University System
- 23 shared
Elżbieta Kierzek
- 21 shared
Durga M. Chadalavada
Pennsylvania State University
- 19 shared
Narayanan Veeraraghavan
Rady Children's Hospital-San Diego
Labs
Bevilacqua LabPI
Awards & honors
- Early Career Award from Society of Biological Inorganic Chem…
- Gordon Hammes Scholar Award (2019)
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