Completed Cells, Biochemistry & Physiology Genetics & Molecular Biology

Nano-Immunology

In plain English

AI plain-English summary

A new generation of microscopes is now powerful enough to track individual molecules moving inside living immune cells. Conventional optical microscopes cannot resolve structures smaller than about half the wavelength of light, which means many crucial molecular interactions on and inside cells remain invisible. This research uses super-resolution techniques—such as STED, RESOLFT, and PALM/STORM—to break that limit, combined with single-molecule detection methods like fluorescence correlation spectroscopy. The goal is to watch, in real time, how proteins and lipids interact during immune responses to infection and cancer. This is fundamental science. It does not aim to produce a new drug or diagnostic test tomorrow. Instead, it will generate a detailed molecular map of immune signalling—showing, for example, exactly how a T-cell receptor clusters when it recognises a threat, or how a pathogen hijacks a host membrane. Such knowledge could eventually guide the design of more precise immunotherapies or vaccines, but the immediate payoff is a deeper understanding of the machinery that governs immunity. Past work in single-molecule imaging has already reshaped fields from neurobiology to materials science; this project extends that power into immunology.

View original technical description
Research by my group aims to unravel nanoscopic changes at the molecular level in living cells to characterise important molecular processes on the cell membrane as well as inside the cell during immunological reactions. Because many cellular responses lead to changes so subtle at the molecular level, studying them requires us to not only observe them with a superior spatial resolution but also to reach a sensitivity that is able to monitor single molecules over time and space. We are using the newest and most powerful super-resolution far-field microscopes (such as STED, RESOLFT or PALM/STORM) to image and analyse cellular structures and protein-protein and protein-lipid interactions at a level of fine detail that until now has not been possible due to the limited spatial resolution of conventional optical far-field microscopes. By combining these super-resolution microscopy techniques with single-molecule sensitive detection methods (such as fluorescence correlation spectroscopy) and fast spatio-temporal tracking tools we are able to see complex dynamic processes otherwise invisible because of the lower power of conventional far-field microscopy. These molecular interactions play an important role in the immune response to infection and cancer and so we intend to use and further develop these advanced microscopy techniques and apply them to gather new insights in immunological research.

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Researchers

Christian Eggeling (Principal Investigator)

Related Research

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Original classification

Intramural

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