Thalhammer S, Stark R W, Müller S, Wienberg J, Heckl W M
Institut Für Kristallographie und Angewandte Mineralogie, Universität München; Germany.
J Struct Biol. 1997 Jul;119(2):232-7. doi: 10.1006/jsbi.1997.3869.
The atomic force microscope (AFM) can be used to visualize and to manipulate biological material with relative case and high resolution. This study was carried out to investigate whether probe sets, specific for subregions of the human genome and useful for the painting of chromosome bands, can be established by PCR amplification of AFM-dissected chromosome regions. Compared to standard microdissection techniques, the AFM can be used with much higher precision for the dissection of the region of interest and subsequent nanoextraction of DNA material. After scanning the area of interest in noncontact mode AFM, chromosome bands were cut by the AFM tip at high force. The genetic material of a single cut attached itself to the tip and was extracted and amplified using degenerate oligonucleotide-primed-PCR. Subsequent to hapten labeling, fluorescence in situ hybridization was performed and chromosome band-specific probes were visualized by standard fluorescence microscopy.
原子力显微镜(AFM)可相对轻松且高分辨率地用于观察和操纵生物材料。本研究旨在调查是否可通过对AFM解剖的染色体区域进行PCR扩增,来建立针对人类基因组亚区域且可用于染色体带描绘的探针组。与标准显微切割技术相比,AFM可更高精度地用于感兴趣区域的切割以及随后DNA材料的纳米提取。在以非接触模式AFM扫描感兴趣区域后,用AFM针尖以高力切割染色体带。单次切割的遗传物质附着在针尖上,随后使用简并寡核苷酸引物PCR进行提取和扩增。在进行半抗原标记后,进行荧光原位杂交,并通过标准荧光显微镜观察染色体带特异性探针。