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基于三维凝胶细胞的微芯片:历史与展望

[Microchips based on three dimensional gel cells: history and perspective].

作者信息

Kolchinskiĭ A M, Griadunov D A, Lysov Iu P, Mikhaĭlovich V M, Nasedkina T V, Turygin A Iu, Rubina A Iu, Barskiĭ V E, Zasedatelev A S

机构信息

Health Front Line, Ltd., Champaign, IL, USA.

出版信息

Mol Biol (Mosk). 2004 Jan-Feb;38(1):5-16.

Abstract

The review describes the history of creation and development of the microchip technology and its role in the human genome project in Russia. The emphasis is placed on the three-dimensional gel-based microchips developed at the Center of Biological Microchips headed by A.D. Mirzabekov since 1988. The gel-based chips of the last generation, IMAGE chips (Immobilized Micro Array of Gel Elements), have a number of advantages over the previous versions. The microchips are manufactured by photo-initiated copolymerization of gel components and immobilized molecules (DNA, proteins, and ligands). This ensures an even distribution of the immobilized probe throughout the microchip gel element with a high yield (about 50% for oligonucleotides). The use of methacrylamide as a main component of the polymerization mixture resulted in a substantial increase of gel porosity without affecting its mechanical strength and stability, which allowed one to work with the DNA fragments of up to 500 nt in length, as well as with rather large protein molecules. At present, the gel-based microchips are widely applied to address different problems. The generic microchips containing a complete set of possible hexanucleotides are used to reveal the DNA motifs binding with different proteins and to study the DNA-protein interactions. The oligonucleotide microchips are a cheap and reliable tool of diagnostics designed for mass application. Biochips have been developed for identification of the tuberculosis pathogen and its antibiotic-resistant forms; for diagnostics of orthopoxviruses, including the smallpox virus; for diagnostics of the anthrax pathogen; and for identification of chromosomal rearrangements in leukemia patients. The protein microchips can be adapted for further use in proteomics. Bacterial and yeast cells were also immobilized in the gel, maintaining their viability, which open a wide potential for creation biosensors on the basis of microchips.

摘要

这篇综述描述了微芯片技术的创建和发展历程及其在俄罗斯人类基因组计划中的作用。重点介绍了自1988年以来由A.D.米尔扎别科夫领导的生物微芯片中心研发的基于三维凝胶的微芯片。最新一代的基于凝胶的芯片,即IMAGE芯片(固定化凝胶元件微阵列),相对于以前的版本具有许多优势。这些微芯片是通过凝胶成分与固定化分子(DNA、蛋白质和配体)的光引发共聚反应制造的。这确保了固定化探针在整个微芯片凝胶元件中均匀分布,产率很高(寡核苷酸约为50%)。使用甲基丙烯酰胺作为聚合混合物的主要成分,在不影响凝胶机械强度和稳定性的情况下,大幅增加了凝胶孔隙率,这使得能够处理长度达500个核苷酸的DNA片段以及相当大的蛋白质分子。目前,基于凝胶的微芯片被广泛应用于解决各种不同问题。包含全套可能的六核苷酸的通用微芯片用于揭示与不同蛋白质结合的DNA基序并研究DNA-蛋白质相互作用。寡核苷酸微芯片是一种设计用于大规模应用的廉价且可靠的诊断工具。已经开发出生物芯片用于鉴定结核病原体及其耐药形式;用于诊断正痘病毒,包括天花病毒;用于诊断炭疽病原体;以及用于鉴定白血病患者的染色体重排。蛋白质微芯片可进一步用于蛋白质组学。细菌和酵母细胞也被固定在凝胶中并保持其活力,这为基于微芯片创建生物传感器开辟了广阔的潜力。

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