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使用脉冲等离子体源对水合蛋白聚糖的超微结构进行研究。

Ultrastructure of hydrated proteoglycans using a pulsed plasma source.

作者信息

Panessa B J, McCorkle R A, Hoffman P, Warren J B, Coleman G

出版信息

Ultramicroscopy. 1981;6(2):139-48. doi: 10.1016/0304-3991(81)90053-x.

DOI:10.1016/0304-3991(81)90053-x
PMID:7022984
Abstract

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.

摘要

在过去10年中,人们尝试在电子显微镜检查期间,通过使用湿室(在环境温度下)[1-3]或冷台(在-30摄氏度及以下)来检查水合生物标本。事实证明,使用这两种方法获得未染色水合生物样品的足够对比度是一个相当大的问题。许多脆弱的生物标本,在水合、冷冻或干燥状态下检查时,会受到电子束的严重损伤,无法通过传统的扫描或透射电子显微镜成像。为了增加标本对比度并消除电子束对标本的损伤,我们开发了一种湿室[4],当与脉冲等离子体软X射线源配合使用时,它能提供完全水合、未染色生物标本的高对比度接触复制品。尽管有人推测水合未染色样品可以通过软X射线接触显微镜成像[5-7],但迄今为止,由于在获得足够成像剂量所需的长时间曝光期间细胞移动或湿样品降解,几乎没有成功的案例[8]。使用本研究中描述的脉冲等离子体源,我们能够使用大约40-60纳秒的曝光时间,同时在大气压下将样品保持在水合状态。通过传统扫描电子显微镜检查时,所得的接触复制品具有良好的对比度和优于30纳米的空间分辨率。

相似文献

1
Ultrastructure of hydrated proteoglycans using a pulsed plasma source.使用脉冲等离子体源对水合蛋白聚糖的超微结构进行研究。
Ultramicroscopy. 1981;6(2):139-48. doi: 10.1016/0304-3991(81)90053-x.
2
Imaging unstained proteoglycan aggregates by soft x-ray contact microscopy.
Ultramicroscopy. 1980;5(3):267-74. doi: 10.1016/0304-3991(80)90031-5.
3
Structure of wet specimens in electron microscopy. Improved environmental chambers make it possible to examine wet specimens easily.电子显微镜下湿标本的结构。改进后的环境舱使轻松检查湿标本成为可能。
Science. 1974 Nov 1;186(4162):407-14. doi: 10.1126/science.186.4162.407.
4
Direct observation of unstained wet biological samples by scanning-electron generation X-ray microscopy.利用扫描电子产生 X 射线显微镜直接观察未染色的湿生物样品。
Biochem Biophys Res Commun. 2010 Jan 1;391(1):198-202. doi: 10.1016/j.bbrc.2009.11.031. Epub 2009 Nov 10.
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Ultrastructural and elemental imaging of biological specimens by soft X-ray contact microscopy.通过软X射线接触显微镜对生物标本进行超微结构和元素成像。
Scan Electron Microsc. 1980(Pt 2):107-16, 78.
6
High-resolution scanning electron microscopy of frozen-hydrated cells.冷冻水合细胞的高分辨率扫描电子显微镜检查。
J Microsc. 1992 Nov;168(Pt 2):169-80. doi: 10.1111/j.1365-2818.1992.tb03259.x.
7
X-ray microanalysis of frozen-hydrated specimens.冷冻水合标本的X射线微分析。
Scan Electron Microsc. 1983(Pt 2):809-26.
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X-ray microscopy: preparations for studies of frozen hydrated specimens.X射线显微镜术:用于研究冷冻水合标本的制备方法。
Scanning Microsc Suppl. 1996;10:349-56; discussion 356-8.
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Progress in scanning electron microscopy of frozen-hydrated biological specimens.冷冻水合生物标本的扫描电子显微镜研究进展。
Scanning Microsc. 1993 Mar;7(1):343-9; discussion 349-50.
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The preparation, examination and analysis of frozen hydrated tissue sections by scanning transmission electron microscopy and x-ray microanalysis.通过扫描透射电子显微镜和X射线微分析对冷冻水合组织切片进行制备、检查和分析。
J Microsc. 1975 Nov;105(2):155-91. doi: 10.1111/j.1365-2818.1975.tb04048.x.

引用本文的文献

1
Contact microscopy with synchrotron radiation.同步辐射光接触显微镜
Biol Trace Elem Res. 1987 Apr;12(1):167-83. doi: 10.1007/BF02796678.