| 1. |
- Norlin, Nils, et al.
(författare)
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Aggregation and fibril morphology of the Arctic mutation of Alzheimer's Aβ peptide by CD, TEM, STEM and in situ AFM
- 2012
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Ingår i: Journal of Structural Biology. - San Diego, CA, USA : Academic Press. - 1047-8477 .- 1095-8657. ; 180:1, s. 174-189
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Tidskriftsartikel (refereegranskat)abstract
- Morphology of aggregation intermediates, polymorphism of amyloid fibrils and aggregation kinetics of the "Arctic" mutant of the Alzheimer's amyloid β-peptide, Aβ((1-40))(E22G), in a physiologically relevant Tris buffer (pH 7.4) were thoroughly explored in comparison with the human wild type Alzheimer's amyloid peptide, wt-Aβ((1-40)), using both in situ atomic force and electron microscopy, circular dichroism and thioflavin T fluorescence assays. For arc-Aβ((1-40)) at the end of the 'lag'-period of fibrillization an abrupt appearance of ∼3nm size 'spherical aggregates' with a homogeneous morphology, was identified. Then, the aggregation proceeds with a rapid growth of amyloid fibrils with a variety of morphologies, while the spherical aggregates eventually disappeared during in situ measurements. Arc-Aβ((1-40)) was also shown to form fibrils at much lower concentrations than wt-Aβ((1-40)): ⩽2.5μM and 12.5μM, respectively. Moreover, at the same concentration, 50μM, the aggregation process proceeds more rapidly for arc-Aβ((1-40)): the first amyloid fibrils were observed after c.a. 72h from the onset of incubation as compared to approximately 7days for wt-Aβ((1-40)). Amyloid fibrils of arc-Aβ((1-40)) exhibit a large variety of polymorphs, at least five, both coiled and non-coiled distinct fibril structures were recognized by AFM, while at least four types of arc-Aβ((1-40)) fibrils were identified by TEM and STEM and their mass-per-length statistics were collected suggesting supramolecular structures with two, four and six β-sheet laminae. Our results suggest a pathway of fibrillogenesis for full-length Alzheimer's peptides with small and structurally ordered transient spherical aggregates as on-pathway immediate precursors of amyloid fibrils.
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| 2. |
- Eriksson, Anna U., et al.
(författare)
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Near infrared optical projection tomography for assessments of beta-cell mass distribution in diabetes research
- 2013
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Ingår i: Journal of Visualized Experiments. - : MyJove Corporation. - 1940-087X. ; 71
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Tidskriftsartikel (refereegranskat)abstract
- By adapting OPT to include the capability of imaging in the near infrared (NIR) spectrum, we here illustrate the possibility to image larger bodies of pancreatic tissue, such as the rat pancreas, and to increase the number of channels (cell types) that may be studied in a single specimen. We further describe the implementation of a number of computational tools that provide: 1/ accurate positioning of a specimen's (in our case the pancreas) centre of mass (COM) at the axis of rotation (AR)2; 2/ improved algorithms for post-alignment tuning which prevents geometric distortions during the tomographic reconstruction2 and 3/ a protocol for intensity equalization to increase signal to noise ratios in OPT-based BCM determinations3. In addition, we describe a sample holder that minimizes the risk for unintentional movements of the specimen during image acquisition. Together, these protocols enable assessments of BCM distribution and other features, to be performed throughout the volume of intact pancreata or other organs (e.g. in studies of islet transplantation), with a resolution down to the level of individual islets of Langerhans.
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| 3. |
- Thim, Jan, et al.
(författare)
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Suitable Post Processing Algorithms for X-Ray Imaging using Oversampled Displaced Multiple Images
- 2011
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Ingår i: Journal of Instrumentation. - 1748-0221. ; 6:2
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Tidskriftsartikel (refereegranskat)abstract
- X-ray imaging systems such as photon counting pixel detectors have a limited spatial resolution of the pixels, based on the complexity and processing technology of the readout electronics. For X-ray imaging situations where the features of interest are smaller than the imaging system pixel size, and the pixel size cannot be made smaller in the hardware, alternative means of resolution enhancement require to be considered. Oversampling with the usage of multiple displaced images, where the pixels of all images are mapped to a final resolution enhanced image, has proven a viable method of reaching a sub-pixel resolution exceeding the original resolution. The effectiveness of the oversampling method declines with the number of images taken, the sub-pixel resolution increases, but relative to a real reduction of imaging pixel sizes yielding a full resolution image, the perceived resolution from the sub-pixel oversampled image is lower. This is because the oversampling method introduces blurring noise into the mapped final images, and the blurring relative to full resolution images increases with the oversampling factor. One way of increasing the performance of the oversampling method is by sharpening the images in post processing. This paper focus on characterizing the performance increase of the oversampling method after the use of some suitable post processing filters, for digital X-ray images specifically. The results show that spatial domain filters and frequency domain filters of the same type yield indistinguishable results, which is to be expected. The results also show that the effectiveness of applying sharpening filters to oversampled multiple images increase with the number of images used (oversampling factor), leaving 60-80% of the original blurring noise after filtering a 6 x 6 mapped image (36 images taken), where the percentage is depending on the type of filter. This means that the effectiveness of the oversampling itself increase by using sharpening filters, and more images taken can be considered worth the effort.
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