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Thesis-PDF - IAP/TU Wien

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Chapter 7<br />

Outlook<br />

The Atomic Force Microscope (AFM) has proven to be a valuable tool for investigation<br />

of biomaterials at the small scale. In this work the single celled alga Euglena<br />

gracilis was investigated in the light of being a bionanotechnological system accommodating<br />

a wealth of functional units within only small volume. A method<br />

for AFM data acquisition of the alga Euglena gracilis was developed and further<br />

investigation can build upon this approach.<br />

As this work is only a beginning of the AFM study of this alga, it focused on its<br />

morphology, on how to obtain first image data of Euglena’s pellicle and some of its<br />

functional cell organelles with potential for technical applications. This undertaking<br />

can be seen as an ignition part in the investigation of algal materials exhibiting<br />

molecular precision achitecture and complexity inherent to living systems.<br />

While the data obtained on whole cells as well as cell organelles provided<br />

essentially morphological data and proved the feasibility of such studies by means<br />

of AFM, other analytical characterization methods, e.g AFM force spectroscopy,<br />

are now possible on these and similar algae by making use of the preparation<br />

method developed herein. Since AFM yields information about the sample as well<br />

as it allows manipulation on the micro and nanoscale, future research attempts<br />

along these lines seem encouraging.<br />

The exact nature of the novel features found, i.e. the indentations in the<br />

center of pellicular strips, should be further analyzed, especially with regards to the<br />

sample preparation techniques used. Equally interesting, AFM force spectroscopy<br />

shall characterize the mucus material ejected by mucus excretion pellicle pores.<br />

Further, elucidation about the three-dimensional structure of the photoreceptor<br />

was attempted with this work, however, the fraction of crystalline parts<br />

contained too few photoreceptors to be found with the AFM tip, since crystalloid<br />

bodies, paramylon grains and not completely removed cell material amounted for a<br />

large portion of the fraction. Possible future approaches comprise the development<br />

of a preparation technique for a solution containing a plentitude of photoreceptors.<br />

92

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