Katharine White

Research Interests

The White Lab is studying how intracellular pH dynamics regulate proteins, pathways and cell behaviors, with approaches across experimental scales. We apply the results of our work to answer fundamental questions about the molecular mechanisms driving cancer cell behaviors and how those mechanisms can be exploited for more effective and safer cancer therapies.

Transient increases in intracellular pH (pHi) are necessary for normal cell processes of cell-cycle progression, migration, and differentiation while dysregulated pHi dynamics are linked to diseases such as neurodegeneration and cancer. While the effects of pHi on global cell behaviors is well established, the proteins and molecular mechanisms that drive these pH-sensitive responses are largely unknown. Furthermore, a lack of tools to directly, specifically, and spatiotemporally manipulate pHi has restricted experiments probing how pH dynamics alter individual cell behaviors. Finally, decreasing pHi can limit tumor progression in some models, but criteria to identify cancer subtypes or patients that would benefit from pHi-lowering drugs are critically needed.

A long-term goal of our research is to understand how protonation events are integrated to induce coordinated changes from proteins, to macromolecular assemblies, to cell behaviors and complex tissue-level effects. To address this goal, we are performing interdisciplinary research across experimental scales. At the molecular scale, we are identifying pH-sensing mechanisms utilized by both wildtype and mutant proteins. At the cellular scale, we are developing new optogenetic tools to spatiotemporally manipulate pHi in living cells to better understand how pHi changes are communicated between cells. At the evolutionary scale, we are interested in understanding how the constitutively increased pHi of cancer shapes the mutational landscape of human cancers.

Selected Publications

• Czowski, B. J.; Marchi, A. N. and White, K. A. "Intracellular pH Regulates β-Catenin with Low pHi Increasing Adhesion and Signaling Functions" 2026 Journal of Biological Chemistry, 302 (3), 111134. DOI: 10.1016/j.jbc.2026.111134.
• Van Dyck, P. K.; Piszkin, L.; Gorski, E. A.; Nascimento, E. T.; Abebe, J. A.; Hoffmann, L. M.; Peng, J. W. and White, K. A. "Ionizable Networks Mediate pH-Dependent Allostery in the SH2 Domain-Containing Signaling Proteins SHP2 and SRC" 2025 Science Signaling, 18 (912), eadt3018. DOI: 10.1126/scisignal.adt3018.
• Lund, L. M.; Marchi, A. N.; Alderfer, L.; Hall, E.; Hammer, J.; Moremen, R.; Asilebo, I.; Trull, K. J.; Hanjaya-Putra, D. and White, K. A. "Intracellular pH Dynamics Respond to Extracellular Matrix Stiffening and Mediate Vasculogenic Mimicry through β-Catenin" 2025 Cell Death & Disease, 16 (1), 720. DOI: 10.1038/s41419-025-08014-z.
• Romero-Moreno, R.; Czowski, B. J.; Harris, L.; Kuehn, J. F. and White, K. A. "Intracellular pH Differentially Regulates Transcription of Metabolic and Signaling Pathways in Normal Epithelial Cells" 2024 Journal of Biological Chemistry, 300 (10), 107658. DOI: 10.1016/j.jbc.2024.107658.
• Spear, J. S. and White, K. A. "Single-Cell Intracellular pH Dynamics Regulate the Cell Cycle by Timing the G1 Exit and G2 Transition" 2023 Journal of Cell Science, 136 (10), jcs260458. DOI: 10.1242/jcs.260458.
• White, K. A.; McEntire, K. D.; Buan, N. R.; Robinson, L. and Barbar, E. "Charting a New Frontier Integrating Mathematical Modeling in Complex Biological Systems from Molecules to Ecosystems" 2022 Integrative and Comparative Biology, 61 (6), pp.2255-2266. DOI: 10.1093/icb/icab165.