H2020Индивидуална стипендия2021–2023

FluoTRAM · Fluorescence-detected Transient Absorption Microscopy

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период: 2021-09-01 → 2023-08-31
Финансиране от ЕС: 144 981 €
Участници: 1
Схема: MSCA-IF

Линиите свързват координатора с партньорите.

Накратко на български

Новият метод комбинира микроскопия и лазерна спектроскопия, за да проследи динамиката на молекулите в биологични проби, например при взаимодействието между протеини. Това помага за по-доброто разбиране на процесите в живите клетки и транспорта на енергия в фотоволтаичните материали.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Fluorescence-detected Transient Absorption Microscopy

The goal of the FluoTRAM (fluorescence-detected transient absorption microscopy) project is to combine techniques of fluorescence microscopy and ultrafast laser spectroscopy in a new method of ultrafast fluorescence microscopy applicable to biological samples. Fluorescence microscopy is an indispensable tool in life sciences and biophysics, where it has been perfected for biological sample imaging either by its autofluorescence or using fluorescent markers such as dyes or fluorescent proteins. For example, it is possible to localize molecules in cells, obtaining information on their local environment and interactions. The fluorescence detection presents a limitation as well, as it provides by its nature information only about on the final, emissive state of the molecules after photoexcitation. Meanwhile, ultrafast nonlinear spectroscopy enables to track the initial state of the molecules after absorption and the following excitation dynamics. However, such techniques typically require volume samples and are detected coherently. In project FluoTRAM, we implement ultrafast nonlinear transient absorption spectroscopy in the fluorescence microscope equipped with fluorescence lifetime imaging. Using the established imaging techniques and probes, Fluorescence-detected TRansient Absorption Microscopy brings the additional information on the excitation event and the dynamics towards the emissive state. This comprehensive additional information will be of great use in life sciences and beyond, with applications for example to dye probes of interaction between proteins or energy and charge transport in materials for photovoltaics.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Fluorescence microscopy is an indispensable tool in many areas of research. In life sciences it has been perfected for biological sample imaging either by its autofluorescence or using fluorescent markers such as dyes or fluorescent proteins. It is thus possible to localize molecules in cells, obtaining wealth of information on their dynamics and environment. Despite its power, the fluorescence detection is, by its nature, limited to the information on the final, emissive state of the molecules after photoexcitation. Meanwhile, transient absorption spectroscopy enables to track the initial state of the molecules after absorption and the following excitation dynamics. However, such ultrafast nonlinear techniques typically require volume samples and coherent detection. We have recently developed a new way to measure transient absorption by detecting the sample fluorescence. In project FluoTRAM we will implement our technique in the fluorescence microscope, where it truly reveals its potential. Using the established imaging techniques and markers, FluoTRAM brings the additional information on the excitation event and the dynamics towards the emissive state. We will implement FluoTRAM in two parallel stages, the time resolution and the spectrally varying excitation. The time resolution will be achieved using chopped laser pulses, varying their delay by a delay stage and recording a difference fluorescence in a pump-probe fashion. The excitation spectrum scanning will be realized interferometrically, creating a phase-stable replica of the excitation pulse and scanning the delay between the two. The comprehensive additional information on the excitation dynamics from absorption to emission will be of great use in life sciences and beyond. Examples include correlation of the excitation and emission spectra (increased Stokes shift vs red shift) for dye probes, intramolecular charge transfer in fluorescent proteins, or charge transfer and recombination in organic materials.

Оригинален текст от CORDIS (на английски).

Участници

UNIVERZITA KARLOVA · Praha 1КоординаторЧехия