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Structural analysis and classification of human metaphase chromosomes by atomic force microscopy

机译:原子力显微镜染色体人中期染色体的结构分析与分类

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We applied atomic force microscopy (AFM) to the analysis and classification of metaphase chromosomes. Human chromosomes were isolated from blood and spread over a glass substrate. We found that air-dried and Giemsa stained chromosomes had a granular surface and the height of approximately 250 nm; however unstained chromosomes had a smooth surface and the height was approximately 100 nm. Giemsa staining caused swelling of the chromosome structure. For the structural analysis, chromosomes were treated with hyaluronidase or a citric acid buffer. The effects of the treatments on chromosomal components, spiral structure and 30-nm solenoid fiber were observed. Each step of G-banding treatments of chromosomes was also visualized by AFM. The trypsin treatment collapsed the chromosomes and subsequent Giemsa staining caused dramatically reswelling of the chromosomes. The height of the G-positive region was approximately 200 nm but the unstained region was approximately 50 nm. The difference in thickness observed was produced by binding of the dye. The AFM image of the banding patterns of treated chromosomes was clearer than the image obtained with an optical microscope. These images made it possible to visualize the karyotyping of chromosomes using AFM. Detection of in situ hybridization using AFM and microdissection of chromosomes using AFM were also investigated.
机译:我们将原子力显微镜(AFM)应用于中期染色体的分析和分类。从血液中分离人染色体并在玻璃基板上铺展。我们发现空气干燥和Giemsa染色体染色体具有颗粒表面和高度约250nm;然而未持有的染色体具有光滑的表面,高度约为100nm。 Giemsa染色引起染色体结构的肿胀。对于结构分析,用透明质酸酶或柠檬酸缓冲液处理染色体。观察到治疗对染色体成分,螺旋结构和30纳米螺线管纤维的影响。 AFM也可视化染色体的每个步骤的染色体处理。胰蛋白酶治疗倒塌染色体和随后的GIEMSA染色,从而显着地转移了染色体。 G阳性区域的高度约为200nm,但未染色的区域约为50nm。观察到的厚度差异是通过染料结合产生的。经处理的染色体的带状图案的AFM图像比用光学显微镜获得的图像更清晰。这些图像使得可以使用AFM来可视化染色体的核型分型。还研究了使用AFM使用AFM和使用AFM的染色体的原位杂交的检测。

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