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MASS MEASUREMENT OF SINGLE MOLECULES WITH THE STEM

MASS MEASUREMENT OF SINGLE MOLECULES WITH THE STEM
使用 STEM 对单分子进行质量测量
批准号:
3103989
负责人:
JOSEPH S WALL
金额:
$27.28万
依托单位国家:
美国
项目类别:
财政年份:
1984
资助国家:
美国
项目状态:
已结题
起止时间:
1984-01-01 至 1988-12-31

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中文摘要
翻译
扫描透射电子显微镜(STEM)可以提供低剂量,
英文摘要
The scanning transmission electron microscope (STEM) can provide low dose, high resolution images of unstained biological samples. Isolated objects or discrete image features can be integrated (after subtraction of substrate) to determine molecular weights and so provide a direct link between biochemistry and electron microscopy. The accuracy of STEM melecular weights improves from about 20% at 10 kD to about 4% at 100 kD and better than 1% above one million D for single particles imaged at a dose of 10 el/Angstroms squared. Practical results on tRNA, nucleosomes, fibrinogen, RNA polymerase, glutamine synthetase, 30s and 50s ribosomal subunits, filamentous viruses and TMV are in good agreement with theoretical predictions. Standard error of the mean can be reduced by averaging over 100-1,000 particles. Histograms of particle mass values can be used to characterize the homogeneity of the preparation. This technique has been applied routinely to a wide variety of users'/collaborators' samples over the past years at the Brookhaven STEM Biotechnology Resource. We propose to continue these productive collaborations and service activities while refining practical aspects of the technique. Further reduction of specimen temperature to 20 K is expected to reduce mass loss below 0.25%/el Angstroms squared now found at 120 K (8x less than at 300 K), permitting higher dose and higher accuracy. Reduction of surface migration at lower temperature is expected to lead to less redistribution of mass during radiation damage. This prediction will be tested using control specimens of known structure (e.g. TMV). A major new thrust will involve use of image averaging programs to improve signal to noise ratio in low dose images. This should permit extension of domainal mass mapping already demonstrated on fibrinogen and dynein to allow detection of the binding of small molecules (1-5 kD) to complexes such as glutamine synthetase and acetylcholine receptor. For particles with spherical or cylindrical symmetry, these programs will also permit determination of mass as a function of radius.
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IMAGE ANALYSIS FOR STEM
ELEMENTAL MAPPING AT LOW DOSE
IMPROVED ACCURACY IN STEM MASS MEASUREMENTS
ELEMENTAL MAPPING AT LOW DOSE
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