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Biomedical subjects

B J Panessa

Publications and source records attributed to B J Panessa.

6 recordsLinked to original sources

Ultrastructure of hydrated proteoglycans using a pulsed plasma source.

During the past 10 years, attempts have been made to examine hydrated biological specimens by using wet chambers (at ambient temperature) [1-3] or cold stages (at -30 degrees C and below) during electron microscopic examination. Obtaining sufficient contrast of unstained hydrated biological samples has proven a considerable problem using both of these methods. Many fragile biological specimens, when examined hydrated, frozen or dried, are severely damaged by the electron beam and cannot be imaged by conventional scanning or transmission electron microscopy. In order to increase specimen contrast and eliminate electron beam induced trauma to the specimen, we have developed a wet-cell [4], which when used in concert with a pulsed plasma soft X-ray source, provides high contrast contact replicas of totally hydrated, unstained biological specimens. Although it has been postulated that hydrated unstained samples can be imaged by soft X-ray contact microscopy [5-7], to date there has been little success due to cell movement or degradation of the wet sample during the long exposure period necessary for an adequate imaging dose [8]. With the pulsed plasma source described in this study we have been able to use exposure times of approximately 40-60 ns while maintaining the sample in its hydrated state at atmospheric pressure. The resultant contact replicas exhibit good contrast and better than 30 nm spatial resolution when examined by conventional scanning electron microscopy.

Chemical Phenomena↗

Imaging unstained proteoglycan aggregates by soft x-ray contact microscopy.

Soft X-ray contact microscopy is a relatively new form of ultrastructural imaging, having better than 6 nm resolution and being uniquely well suited for the examination of fragile, unstained biological specimens. The biological specimen placed on a layer of photoresist and exposed to soft X-rays (1-10 nm lambda) of a specific wavelength or broad band. After X-ray exposure, the specimen is removed from the photoresist and the latter chemically developed. When the developed replica is examined by high resolution scanning electron microscopy, the fine structure of the original biological specimen is faithfully reproduced. Since the soft X-ray replica is initially formed due to the differential absorption of the incident X-rays by the biological specimen, the resultant contact replica also reveals information about the elemental composition of the sample. This paper presents our application of this new technique for the study of the proteoglycans, the complex polyanionic macromolecules comprising the gel phase in the matrix of mammalian cartilage.

Animals↗

Ultrastructural and elemental imaging of biological specimens by soft X-ray contact microscopy.

Soft X-ray contact microscopy offers a means of visualizing unstained as well as stained biological materials at better than 6 nm resolution. Unlike light and transmission electron microscopy, which rely on stains to increase specimen contrast, soft X-ray imaging is dependent upon the differential absorption of incident soft (1-10nm wavelength) X-rays by the endogenous elements within the specimen. The advantages of using soft X-rays for imaging are: 1) reduced specimen damage during exposure; 2) ability to image hydrated specimens at atmospheric pressure; 3) ability to image specimens ranging in thickness from less than 40 nm to as much as 10 microns; and 4) ability to map the elemental composition of the specimen through observation of the differential absorption of properly chosen incident x-ray wave lengths. This paper explains the principles of the image formation and demonstrates the use of soft X-ray contact microscopy with biological samples which could not readily be imaged in their natural form using conventional electron microscopy methods.

Animals↗

High-resolution soft x-ray microscopy.

X-ray micrographs of biological materials have been obtained with a resolution better than 100 angstroms by using x-ray resist as the recording medium. A high-resolution scanning electron microscope with a short-focal-length final lens, operating in the "low-loss" mode, is used to make the smallest features in the x-ray replica visible.

Animals↗

High-resolution scanning electron microscopy of bacteriophages 3C and T4.

An account is presented of the design and operation of a new scanning electron microscopic, and its first application to the study of biological samples. Bacteriophages were chosen because much of their ultrastructure is beyond the resolution of the conventional scanning electron microscope. The new instrument permits examination of bulk samples with a resolution that exceeds, by at least a factor of 2.5, the resolution obtained in the best secondary electron scanning electron microscopes using high brightness guns, and exceeds by an order of magnitude the resolution of standard scanning electron microscopes using tungsten filament guns. It also permits examination of biological samples in scanning transmission mode at resolutions similar to conventional transmission electron microscopes.

Coliphages↗