Author

J. P. McGee

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

Biochemistry· 3 Cell Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 4 Assay:proteomics· 4 Research Focus:cell type annotation· 3 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:deep learning· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

N. L. Kelleher· 3 shared R. D. Melani· 2 shared A. Sebastian· 1 shared B. P. Early· 1 shared B. S. Drown· 1 shared E. K. Neumann· 1 shared F. A. Butun· 1 shared J. B. Greer· 1 shared

Activity by Year

2019-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 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

3 shared papersBiochemistry

N. L. Kelleher

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

PfCAP-H is essential for assembly of condensin I complex and karyokinesis during asexual proliferation of Plasmodium falciparum

P. Gurung, J. P. McGee, J. D. Dvorin

This study investigates the role of PfCAP-H in condensin I complex assembly and karyokinesis during Plasmodium falciparum asexual proliferation, finding it essential for structural integrity and proper cell division.

bioRxiv · Feb 26, 2024 · PreprintCell Biology

Global Release of Translational Repression Across Plasmodiums Host-to-Vector Transmission Event

K. T. Rios, J. P. McGee, A. Sebastian, R. L. Moritz, M. Feric, S. Absalon, K. E. Swearingen, S. E. Lindner

This study identifies the global release of translational repression in Plasmodium parasites during host-to-vector transmission using transcriptomics and proteomics.

bioRxiv · Feb 1, 2024 · PreprintMicrobiology

Direct Imaging and Identification of Proteoforms up to 70 kDa from Human Tissue

P. Su, J. P. McGee, K. R. Durbin, M. A. R. Hollas, M. Yang, E. K. Neumann, J. L. Allen, B. S. Drown, F. A. Butun, J. B. Greer, B. P. Early, R. T. Fellers, J. M. Spraggins, J. Laskin, J. M. Camarillo, , N. L. Kelleher

This paper introduces PiMS, a method that detects proteoforms up to 70 kDa in human tissue with high spatial resolution, identifying key metabolic enzymes in kidney tissue.

bioRxiv · Dec 7, 2021 · PreprintBiochemistry

Standard Procedures for Native CZE-MS of Proteins and Protein Complexes up to 800 kDa

K. Jooss, J. P. McGee, R. D. Melani, N. L. Kelleher

The paper provides standard operating procedures for native capillary electrophoresis mass spectrometry (nCZE-MS) to improve reproducibility and data quality for large proteins and complexes.

bioRxiv · Nov 2, 2020Biochemistry

Direct Measurement of Light and Heavy Antibody Chains Using Differential Ion Mobility Spectrometry and Middle-Down Mass Spectrometry

R. D. Melani, K. Srzentic, V. R. Gerbasi, J. P. McGee, R. Huguet, L. Fornelli, N. L. Kelleher

This paper introduces a rapid FAIMS tandem MS method for characterizing monoclonal antibody light and heavy chains, reducing analysis time by 40-60% compared to LC-MS/MS.

bioRxiv · Jul 5, 2019Biochemistry