Author

J. L. Camberg

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

Biology Disciplines

Click to filter author papers

Microbiology· 5 Cell Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:E. coli· 6 Approach:experimental assay· 6 Research Focus:cell signaling & trafficking· 5 Assay:proteomics· 5 Research Focus:cell type annotation· 2 Approach:wet-lab / biochemical assay· 2 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1

Frequent Co-Authors

J. J. Morrison· 4 shared E. C. DiBiasio· 3 shared C. E. Trebino· 2 shared C. J. LaBreck· 2 shared C. N. Ferreira· 2 shared D. C. Rowley· 2 shared J. Conti· 2 shared P. S. Cohen· 2 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

4 shared papersMicrobiology

J. J. Morrison

Mutual co-authors in cluster

Author profile →

6 papers

Recent·Most cited

Metabolic flux regulates growth transitions and antibiotic tolerance in uropathogenic Escherichia coli

J. J. Morrison, D. A. Banas, E. K. Madden, E. C. DiBiasio, D. C. Rowley, P. S. Cohen, J. L. Camberg

This study shows that metabolic flux in the TCA cycle regulates quiescence and antibiotic tolerance in UPEC, with ZapE and IHF playing key roles in this process.

bioRxiv · May 9, 2023 · PreprintCell Biology

Active site mutations in the bacterial actin homolog FtsA impair direct interactions with the divisome in Escherichia coli

J. J. Morrison, C. N. Ferreira, E. M. Siler, K. Nelson, C. E. Trebino, B. Piraino, J. L. Camberg

This study identifies key residues in FtsA critical for ATP hydrolysis, phospholipid binding, and membrane interactions, showing their role in Z-ring assembly and cell division in E. coli.

bioRxiv · Feb 25, 2022 · PreprintMicrobiology

An enhancer sequence in the intrinsically disordered region of the essential cell division protein FtsZ promotes conformation-guided substrate processing by ClpXP in Escherichia coli

M. G. Viola, T. M. Perdikari, C. Trebino, N. Rahmani, K. L. Mathews, C. M. Pena, X. Y. Chua, B. Xuan, C. J. LaBreck, N. L. Fawzi, J. L. Camberg

The paper shows that an intrinsically disordered region of FtsZ enhances ClpXP-mediated degradation through conformational interactions.

bioRxiv · Jan 14, 2021 · PreprintMicrobiology

Coregulated assembly of actin-like FtsA polymers with FtsZ during Z-ring formation and division in Escherichia coli

J. J. Morrison, J. Conti, J. L. Camberg

This study investigates how FtsA and FtsZ coassemble during Z-ring formation in E. coli, showing that FtsA ATP hydrolysis and phospholipid interactions are essential for Z-ring assembly and division.

bioRxiv · Jan 12, 2021 · PreprintMicrobiology

Disassembly and degradation of MinD oscillator complexes by Escherichia coli ClpXP

C. J. LaBreck, C. E. Trebino, C. N. Ferreira, J. J. Morrison, E. C. DiBiasio, J. Conti, J. L. Camberg

This study shows that ClpXP degrades MinD in vitro and in vivo, affecting Min function during stationary phase.

bioRxiv · Jan 9, 2020Microbiology

Peptidoglycan sensing prevents quiescence and promotes quorum-independent growth of uropathogenic Escherichia coli

E. C. DiBiasio, H. J. Ranson, J. R. Johnson, D. C. Rowley, P. S. Cohen, J. L. Camberg

This study shows that peptidoglycan sensing prevents quiescence and promotes growth in uropathogenic E. coli, with L-lysine and PG peptides acting as proliferants.

bioRxiv · Nov 4, 2019 · PreprintMicrobiology