Advances in scanning force microscopy of biological structures

<p> A multifacted approach to the imaging of biological structures by scanning force microscopy is described. The major problems addressed are the distortion of biological samples by excessive forces applied by the cantilever stylus and sample motion relative to the imaging substrate.</p>...

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Main Author: Clark, Steven Manning
Format: Others
Language:en
Published: 1993
Online Access:https://thesis.library.caltech.edu/7275/1/Clark_sm_1993.pdf
Clark, Steven Manning (1993) Advances in scanning force microscopy of biological structures. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/0vhp-pk35. https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776 <https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776>
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spelling ndltd-CALTECH-oai-thesis.library.caltech.edu-72752021-04-20T05:01:40Z https://thesis.library.caltech.edu/7275/ Advances in scanning force microscopy of biological structures Clark, Steven Manning <p> A multifacted approach to the imaging of biological structures by scanning force microscopy is described. The major problems addressed are the distortion of biological samples by excessive forces applied by the cantilever stylus and sample motion relative to the imaging substrate.</p> <p> The first two chapters discuss the design of digital signal processor based scanning force microscope control electronics and a novel microscope head that eliminates the application of excessive forces to the sample caused by electronic or vibrational noise.</p> <p> The third chapter presents a novel use of chemical vapor deposition for application of heterofunctional alkoxysilanes to scanning force microscopy imaging subsrates. This technique provides imaging substrates which have chemical groups that can be used for sample immobilization without compromising substrate smoothness. The use of the chemically derivatized substrates for scanning force microscopy is also explored.</p> <p> The final chapter presents high resolution images of bovine liver catalase micro-crystals. The images of the protein micro-crystals show resolution on the order of 2 to 3 nanometers allowing the visualization of individual catalase tetramers. To our knowledge this is the first report of images of protein micro-crystals taken by scanning force microscopy which have resolution comparable to that of electron microscopy.</p> 1993 Thesis NonPeerReviewed application/pdf en other https://thesis.library.caltech.edu/7275/1/Clark_sm_1993.pdf Clark, Steven Manning (1993) Advances in scanning force microscopy of biological structures. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/0vhp-pk35. https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776 <https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776> https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776 CaltechTHESIS:11192012-103302776 10.7907/0vhp-pk35
collection NDLTD
language en
format Others
sources NDLTD
description <p> A multifacted approach to the imaging of biological structures by scanning force microscopy is described. The major problems addressed are the distortion of biological samples by excessive forces applied by the cantilever stylus and sample motion relative to the imaging substrate.</p> <p> The first two chapters discuss the design of digital signal processor based scanning force microscope control electronics and a novel microscope head that eliminates the application of excessive forces to the sample caused by electronic or vibrational noise.</p> <p> The third chapter presents a novel use of chemical vapor deposition for application of heterofunctional alkoxysilanes to scanning force microscopy imaging subsrates. This technique provides imaging substrates which have chemical groups that can be used for sample immobilization without compromising substrate smoothness. The use of the chemically derivatized substrates for scanning force microscopy is also explored.</p> <p> The final chapter presents high resolution images of bovine liver catalase micro-crystals. The images of the protein micro-crystals show resolution on the order of 2 to 3 nanometers allowing the visualization of individual catalase tetramers. To our knowledge this is the first report of images of protein micro-crystals taken by scanning force microscopy which have resolution comparable to that of electron microscopy.</p>
author Clark, Steven Manning
spellingShingle Clark, Steven Manning
Advances in scanning force microscopy of biological structures
author_facet Clark, Steven Manning
author_sort Clark, Steven Manning
title Advances in scanning force microscopy of biological structures
title_short Advances in scanning force microscopy of biological structures
title_full Advances in scanning force microscopy of biological structures
title_fullStr Advances in scanning force microscopy of biological structures
title_full_unstemmed Advances in scanning force microscopy of biological structures
title_sort advances in scanning force microscopy of biological structures
publishDate 1993
url https://thesis.library.caltech.edu/7275/1/Clark_sm_1993.pdf
Clark, Steven Manning (1993) Advances in scanning force microscopy of biological structures. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/0vhp-pk35. https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776 <https://resolver.caltech.edu/CaltechTHESIS:11192012-103302776>
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