More information
Portrait Xingbo Yang

Biological systems display self-organization across scales, from the assembly of subcellular structures to morphogenesis in development. Biological self-organization is characterized by the emergence of order from the interactions among its building blocks, such as molecules and cells. These processes are intrinsically out of equilibrium and driven by energy flows at the scale of its building blocks. It remains a fundamental question to understand how order and structures emerge from interacting building blocks in such processes. While extensive research is being conducted to explore the contribution of gene regulation, signaling and mechanical forces to biological self-organization, much less is known about the contribution of energetics in such processes. My group aims to address fundamental questions in the bioenergetics of self-organization, including:

  • What are the energetic costs of fundamental cellular processes, such as cell division, cell motility, ion homeostasis, biosynthesis and information processing?
  • How do cellular energy expenditures vary in space and time and how do cells control energetic fluxes spatiotemporally?
  • What are the energetic constraints and tradeoffs associated with biological self-organization?
  • What are the impacts of energetic variations and perturbations in physiological and pathological conditions?

Metabolism supplies free energy for cells. Our group is developing quantitative imaging techniques to measure metabolic activities in living cells, enabling the characterization of spatiotemporal dynamics of metabolic pathways with single-cell and even subcellular resolution. We are combining biophysical modeling with quantitative metabolic imaging to study biological self-organization by exploring the spatiotemporal variation of metabolic activities in cells, tissues and organisms.

Xingbo Yang Research: Figure
Figure: [Upper left] mitochondrial metabolism displays a spatial gradient associated with meiotic spindle in mouse oocyte. Heatmap displays the fluorescence lifetime of NADH measured from fluorescence lifetime imaging microscopy (FLIM). [Upper right] meiotic spindle disassembles reversibly upon oxygen drop and recovery. [Lower panel] heatmaps of NADH fluorescence lifetime during early mouse embryo development. Inner cell mass (ICM) and trophectoderm (TE) display distinct metabolic profiles. Scale bar 20μm.

Future Projects and Goals

  • Combine biophysical modeling with quantitative metabolic imaging to quantify the energetic costs of key cellular processes and to understand how metabolic fluxes are distributed across the cell.
  • Understand how perturbations of energy metabolism impact spindle self-organization in meiotic and mitotic cells.
  • Characterize the spatiotemporal dynamics of metabolism in development and explore the impact of metabolic variations on cell motility, proliferation and cell fate specification.

Methodological and Technical Expertise

  • Quantitative live cell metabolic imaging (e.g. two-photon confocal fluorescence lifetime imaging)
  • Biochemical measurements of cell metabolism (e.g. oxygen consumption rate, nutrient uptake rate)
  • Retrieval, culturing and microinjection of oocytes and embryos
  • Quantitative image analysis
  • Computation and mathematical modeling of living systems

CV

As of February 2023
Research Group Leader at Cluster of Excellence Physics of Life, TU Dresden

2017–2022
Postdoctoral Fellow, Department of Molecular and Cellular Biology and School of Engineering and Applied Sciences, Harvard University, USA

2015–2017
Postdoctoral Fellow, Department of Physics, Northwestern University, USA

2010–2015
Ph.D. Physics, Syracuse University, USA

More Information

Yang Group at PoL

Selected Publications

Easun Arunachalam*, William Ireland*, Xingbo Yang*, and Daniel Needleman
Dissecting flux balances to measure energetic costs in cell biology: techniques and challenges.
Annual Review of Condensed Matter Physics 14 (2023)

Venturas, Marta, Jaimin S. Shah, Xingbo Yang, Tim H. Sanchez, William Conway, Denny Sakkas, and Dan J. Needleman
Metabolic state of human blastocysts measured by fluorescence lifetime imaging microscopy.
Human Reproduction 37, no. 3, 411–427 (2022)

Venturas, Marta, Xingbo Yang, Kishlay Kumar, Dagan Wells, Catherine Racowsky, and Daniel J. Needleman
Metabolic imaging of human cumulus cells reveals associations among metabolic profiles of cumulus cells, patient clinical factors, and oocyte maturity. 
Fertility and sterility 116, no. 6, 1651–1662 (2021)

Xingbo Yang, Gloria Ha, and Daniel J. Needleman
A coarse-grained NADH redox model enables inference of subcellular metabolic fluxes from fluorescence lifetime imaging.
Elife 10: e73808 (2021)

Xingbo Yang*, Matthias Heinemann, Jonathon Howard, Greg Huber, Srividya Iyer-Biswas, Guillaume Le Treut, Michael Lynch, Kristi L. Montooth, Daniel J. Needleman, Simone Pigolotti, Jonathan Rodenfels, Pierre Ronceray, Sadasivan Shankar, Iman Tavassoly, Shashi Thutupalli, Denis V. Titov, Jin Wang, and Peter J. Foster*
Physical bioenergetics: Energy fluxes, budgets, and constraints in cells.
Proceedings of the National Academy of Sciences 118, no. 26: e2026786118 (2021)

*equal contribution