Macromolecules imaging

An experimental teclmique that is usefiil for structure studies of biological macromolecules and other crystals with large unit cells uses neither the broad, white , spectrum characteristic of Lane methods nor a sharp, monocliromatic spectrum, but rather a spectral band with AX/X 20%. Because of its relation to the Lane method, this teclmique is called quasi-Laue. It was believed for many years diat the Lane method was not usefiil for structure studies because reflections of different orders would be superposed on the same point of a film or an image plate. It was realized recently, however, that, if there is a definite minimum wavelengdi in the spectral band, more than 80% of all reflections would contain only a single order. Quasi-Laue methods are now used with both neutrons and x-rays, particularly x-rays from synclirotron sources, which give an intense, white spectrum. 

Tang S L, McGhie A J and Suna A 1993 Molecular-resolution imaging of insulating macromolecules with the scanning tunnelling microscope via a nontunnelling, electric-field-induced mechanism Phys. Rev. B 47 3850... 

Krausch G, Hipp M, Bditau M, Mlynek J and Marti O 1995 High resolution imaging of polymer surfaces with chemical sensitivity Macromolecules 28 260... 

IMB Jena Image Library of Biological Macromolecules http //www.imb-jena.de/lMAGE.htmi... 

Hyde, PD Ediger, MD, NMR Imaging of Diffusion of Small Organic Molecules in Silk Fibroin Gel, Macromolecules 24, 620, 1991. 

Sample preparation for AFM analysis is relatively simple. Generally, a desired amount of sample is absorbed onto a smooth and clean substrate surface, for example, a freshly cleaved mica surface. For example, to prepare a food macromolecule sample for AFM imaging in air, the diluted macromolecule solution is disrupted by vortexing. Then, a small aliquot (tens of microliters) of vortexed solution is deposited onto a surface of freshly cleaved mica sheet by pipette. The mica surface is air dried before the AFM scan. A clean surrounding is required to avoid the interference of dust in the air. Molecular combing or fluid fixation may be applied to manipulate the molecule to get more information. 

M. J. McCarthy, R. L. Powell 2001, (Polymer melt rheology by magnetic resonance imaging), Macromolecules 34, 5520. 

Fig. 3.5 Representation of a scheme of an experiment (upper set of drawings) and the obtained experimental results presented as AFM images (middle part) and cross-sectional profiles (bottom) that provides evidence of silica nucleation and shell formation on biopolymer macromolecules. Scheme of experiment. This includes the following main steps. 1. Protection of the mica surface against silica precipitation. It was covered with a fatty (ara-chidic) acid monolayer transferred from a water substrate with the Langmuir-Blodgett technique. This made the mica surface hydrophobic because of the orientation of the acid molecules with their hydrocarbon chains pointing outwards. 2. Adsorption of carbohydrate macromolecules. Hydrophobically modified cationic hydroxyethylcellulose was adsorbed from an aqueous solution. Hydrocarbon chains of polysaccharide served as anchors to fix the biomacromolecules firmly onto the acid monolayer. 3. Surface treatment by silica precursor. The mica covered with an acid mono-...

Flowever, the object being analyzed has to be removed from the tissues. Thus, information about the distribution of the target in the organism or in the cells is inevitably lost. What is now needed is a technology to acquire information about the distribution of the biomolecule simultaneously with its identification. The method used for this purpose, called imaging mass spectrometry (IMS), is as follows. The tissue sample is cut into thin slices, and a matrix that assists the ionization of macromolecules is spread onto these slices. The macromolecules are then ionized by a scanning laser, and the generated ions are detected and analyzed by MS.1... 

SIMS imaging was theoretically invented in 1949 by Herzog and Viehb of the Vienna University in Austria. The first SIMS device was completed by Liebel and Herzog in 1961 with the support of the National Aeronautics and Space Administration (NASA) and was used to analyze metal surfaces. However, it was not suitable for analyzing biological macromolecules because the second electronic ion beam breaks the molecules into atoms. 

Confocal scanning Examination of cells in Cryoelectron Imaging of biological macromolecules in the... 

Dark field Visualization technique for ashes produced by microincineration and fluorescence microscopy useful for low-contrast subjects Electron systems imaging EM shadowing Detection, localization, and quantitation of light elements Structural information from ordered arrays of macromolecules... 

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