HEIndividual fellowship2022–2025

CoCoPro · high-Coherence, ultraCold electron diffraction for molecular movies of membrane Proteins

Horizon Europe — Marie Skłodowska-Curie Actions

Duration
2022-09-15 → 2025-05-14
EU contribution
€254,330
Participants
2
Scheme
HORIZON-TMA-MSCA-PF-EF

Lines connect the coordinator with its partners.

Results in brief

high-Coherence, ultraCold electron diffraction for molecular movies of membrane Proteins

On a molecular level, all biological processes are carried out by proteins. Membrane proteins act as pumps and gates in the cell membrane, thus controlling all traffic that enters and leaves the cell. Because of this, they are important targets for medicine while their malfunctioning is at the heart of a plethora of diseases. But despite their enormous importance, membrane proteins are poorly understood as they are notoriously difficult to study using traditional methods based on X-rays. The more recently developed method of cryo-electron microscopy has revealed the structures of some of these proteins, but as it requires the sample to be frozen the obtained images are inherently static. Now imagine that we could have an instrument that allows making movies of such proteins, so we can see exactly how they work and, also, why sometimes they do not work. Such a tool could revolutionize biochemistry, giving a unique insight in the structure-function relationship of nature’s molecular machinery, and helping scientists to understand membrane-protein-related diseases. To make these molecular movies, I use a unique source that produces ultrashort flashes of electrons. Each of these flashes takes a snapshot of the protein, and together these snapshots form a molecular movie of the conformational change of the protein. To resolve the protein at high resolution while limiting radiation damage, the snapshots are taken in the form of diffraction patterns from 2D protein crystals. For this to work, the wave nature of the electrons needs to be very pronounced, i.e. the electron bunch needs a good coherence. To obtain such high-quality electron bunches, I use a unique approach: in a vacuum, Rubidium atoms are first laser-cooled to almost absolute zero temperature and then carefully ionized with a femtosecond laser pulse. The thus produced ultracold electron bunches are sufficiently coherent to create diffraction patterns from the protein crystal. In summary, by combining principles from fundamental physics with state-of-the-art technology and biochemistry, I aim to deliver a proof of concept that on the long term will advance medicine and other research fields through an improved understanding of membrane proteins.

Data: CORDIS, © European Union

Project objective

Imagine we could make movies of proteins in action. In this project, I propose to develop a unique, table-top setup based on the diffraction of ultracold electrons that does exactly that: make molecular movies of proteins, in particular of the important class of membrane proteins. This tool could revolutionize biochemistry, yielding an ultimate view of natures molecular machinery, and helping scientists to understand membrane-protein-related diseases and develop highly targeted medicines.A unique source, developed at the TU/e and based on the femtosecond photoionization of an ultracold gas, generates electron pulses that should in principle be sufficiently short, intense and coherent to enable electron diffraction on 2D crystals of membrane proteins. In this project I will evaluate the sources capability to generate high-quality diffraction patterns from 2D crystals of e.g. hydrophobin and bacteriorhodopsin. Next, I will measure a sequence of such diffraction patterns in a pump-probe experiment, to obtain a molecular movie of the light-induced conformational change of bacteriorhodopsin. This will be the first protein molecular movie ever obtained on a table-top setup. In parallel, I will improve the source performance. Accelerating the electrons to higher energies (from 10 to above 100 keV), I can keep the sample in its native, aqueous environment inside a Liquid Cell, which strongly extends the applicability of the setup. Modifying the spatial and spectral properties of the ionization laser, I expect to be able to increase the number of electrons per pulse, allowing single-shot diffraction patterns, and to further increase transverse coherence, reducing the required crystal size. Finally, I will seek to improve the coherence of the source to the point where I can apply my experience in Coherent Diffractive Imaging to make molecular movies of a single protein, without crystallization, which is a holy grail in structural dynamics, all on a table-top setup.

Original text from CORDIS.

Participants

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Data: CORDIS, © European Union