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Lipid membranes define the boundaries of life. Membranes thus determine how a cell communicates with its environment. The integrity and surface properties of membranes are particularly important in hostile environments such as those experienced by bacterial pathogens inside their hosts. While eukaryotic membranes have been extensively studied and modeled, comparatively little is understood about the lipid membranes of pathogens such as Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis.
We are applying biochemical, microbiological and biophysical methods to fundamental questions in bacterial membrane biogenesis as they relate to mycobacteria in general and Mtb in particular. We are also developing and applying chemical tools that enable us to study processes in the bacterial cell envelope specifically and accurately.
Mycobacteria generate many structurally complex and unusual lipids. Many are associated with virulence, but few have received molecular-level scrutiny in the membrane context. In particular the mechanisms by which lipids are transported to the specialized outer layer, or mycomembrane, are not well understood. The JSeeliger group is pursuing several questions that address these issues:
- What are the molecular mechanisms underlying mycomembrane assembly?
- How do these pathways contribute to cell growth, division and size determination?
- How can we subvert lipid biosynthesis and membrane assembly pathways for antimicrobial therapy?
Our team comprises scientists with a broad range of expertise. We welcome new members who have interests and experience ranging from synthetic chemistry to biophysics to microbiology. Contact Jessica for more information about joining the lab.
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Collaborations and top research areas from the last five years
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Chemical Biology Training Interface Year 7
Boon, E. (PI) & Seeliger, J. (CoPI)
National Institute of General Medical Sciences
07/1/26 → 06/30/27
Project: Research
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Uncovering Interactions of the Atypical Lipid Transporter Rv1410c with its Substrates and the Lipid Carrier LprG in Mycobacterium Tuberculosis
Seeliger, J. (PI) & Jaisinghani, N. (CoI)
National Institute of Allergy & Infectious Disease
06/24/26 → 05/31/28
Project: Research
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Untangling the Inner Workings of the Mycobacterial Cell Envelope
Seeliger, J. (PI)
National Institute of General Medical Sciences
06/1/26 → 05/31/27
Project: Research
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Tracking the Hierarchical Secretion of ESX-1 Substrates Through the Mycobacterial Cell
Seeliger, J. (PI)
National Institute of Allergy & Infectious Disease
02/1/25 → 01/31/27
Project: Research
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NRSA for Isabel Sakarin: Rv3802c function in mycobacterial cell envelope remodeling, barrier properties, and antibiotic susceptibility
Seeliger, J. (PI) & Sakarin, I. (CoPI)
National Institute of Allergy & Infectious Disease
08/1/24 → 07/31/27
Project: Research
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Measuring Membrane Fluidity in Live Mycobacteria Reveals Subcellular Lateral Variation And Pole-Selective Responses to Mycomembrane Perturbation
Sakarin, I., Clabeaux, C., Parkin, L. A. & Seeliger, J. C., Feb 13 2026, In: ACS Infectious Diseases. 12, 2, p. 637-652 16 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Mucin degradation by Akkermansia muciniphila promotes Alistipes-dependent tryptophan metabolism and Th17-driven autoimmunity
Lin, X., Singh, A., Shan, X., Tawch, S., Sakarin, I., Bahadur, T., McLinskey, N., Melville, P., Fries, B. C., Coyle, P. K., Collins, J., Morgun, A., Shulzhenko, N., Seeliger, J., Hand, T. W., Xia, L., Syritsyna, O. & Kumar, P., 2026, (Accepted/In press) In: Mucosal Immunology. 100377.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Tagging lipoproteins in mycobacteria via metabolic incorporation of modified fatty acids
Becker, K. L., Maceren, J. P., Parkin, L. A. & Seeliger, J. C., Jan 2026, Lipids and Membranes: Dynamics and Interorganelle Lipid Transport. Baskin, J. M. (ed.). Academic Press Inc., p. 161-177 17 p. (Methods in Enzymology; vol. 727).Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review
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Discovery of 2,4,5-Substituted Benzoxazole Derivatives as Pks13 Inhibitors via the Scaffold Hopping Strategy
Obadawo, B. S., Bartolomeu Halicki, P. C., Becker, K. L., Seeliger, J. C., Rohde, K. H. & Sucheck, S. J., Jun 13 2025, In: ACS Infectious Diseases. 11, 6, p. 1460-1472 13 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Scopus citations -
Identifying Inhibitor Targets in Mycobacteria by Activity-Based Probe Profiling
Jaisinghani, N., Sakarin, I., Patel, H. V., Li, M., Previti, M. L. & Seeliger, J. C., 2025, Methods in Molecular Biology. Humana Press Inc., p. 139-154 16 p. (Methods in Molecular Biology; vol. 2921).Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review