Click on the picture for a larger version Left: Maximum-intensity projection of a 3D SPIM data set of a microtubule aster in high-speed interphasic Xenopus laevis egg extract. The 3D image stack contains 68 planes at 300 nm spacing. Tubulin labelled with TAMRA. Detection via Carl Zeiss W 100x/1.0 lens. Right: 3D reconstruction of the microtubule aster with custom automated image processing routines. Green traces indicate microtubules that were partly located outside the recording volume. For those traces the last cross does not correspond to the plus-end, but rather to the position at which the tracing algorithm recognized an intersection of the microtubule's contour with the recording volume's boundaries. Red traces indicate MTs that were located fully inside the recording volume.

Press Release 10 September 2007 [PDF]

Scientists from the European Molecular Biology Laboratory [EMBL] have developed a new method to prepare and image biological samples in three dimensions with laser light-sheet based fluorescence microscopy. The technological advance, which is published in the current online issue of Nature Methods, allows for the first time the observation of the intrinsic dynamic properties of microtubules. These constitute a major part of the cell's skeleton and can now be observed in a mechanically unconstrained and at the same time physiologically relevant context.

Microtubules form a network of protein filaments, which constantly grow and shrink. This network's behaviour is controlled by the intrinsic properties of many different proteins. Conventional microscopy studies microtubules and other filaments in artificial set-ups, which biases certain behaviour and introduces artefacts via the hard and flat surfaces of the surrounding glass chamber. Ernst Stelzer and his colleagues Philipp Keller and Francesco Pampaloni at EMBL have managed to overcome the limitations of traditional microscopy and discovered different microtubule behaviour in an unrestricted environment, resulting in a highly accurate characterisation of intrinsic microtubule dynamics in a close to life context.

The new method is currently being adopted to study other dynamic cellular processes. The authors expect their results to have a major impact on the understanding of the mechanical properties of tissue cells. This will also influence current nanobiotechnology and have a significant effect on cancer research.

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