Suppr超能文献

使用微电子蛋白质-DNA芯片形式对基因片段进行快速并行突变扫描。

Rapid parallel mutation scanning of gene fragments using a microelectronic protein-DNA chip format.

作者信息

Behrensdorf Heike A, Pignot Marc, Windhab Norbert, Kappel Andreas

机构信息

Nanogen Recognomics GmbH, Industriepark Hoechst, Building G830, 65926 Frankfurt am Main, Germany.

出版信息

Nucleic Acids Res. 2002 Jul 15;30(14):e64. doi: 10.1093/nar/gnf063.

Abstract

We have developed a method for the de novo discovery of genetic variations, including single nucleotide polymorphisms and mutations, on microelectronic chip devices. The method combines the features of electronically controlled DNA hybridisation on open-format microarrays, with mutation detection by a fluorescence-labelled mismatch- binding protein. Electronic addressing of DNA strands to distinct test sites of the chip allows parallel analysis of several individuals, as demonstrated for mutations in different exons of the p53 gene. This microelectronic chip-based mutation discovery assay may substitute for time-consuming sequencing studies and will complement existing technologies in genomic research.

摘要

我们已经开发出一种在微电子芯片设备上从头发现遗传变异(包括单核苷酸多态性和突变)的方法。该方法将开放式微阵列上电子控制的DNA杂交特性与荧光标记的错配结合蛋白进行突变检测相结合。将DNA链电子寻址到芯片的不同测试位点可对多个个体进行平行分析,如对p53基因不同外显子中的突变所做的演示。这种基于微电子芯片的突变发现检测方法可能会替代耗时的测序研究,并将补充基因组研究中的现有技术。

相似文献

1
Rapid parallel mutation scanning of gene fragments using a microelectronic protein-DNA chip format.
Nucleic Acids Res. 2002 Jul 15;30(14):e64. doi: 10.1093/nar/gnf063.
3
A novel optical biosensor format for the detection of clinically relevant TP53 mutations.
Biosens Bioelectron. 2005 May 15;20(11):2310-3. doi: 10.1016/j.bios.2004.11.020.
4
The use of immobilized mismatch binding protein in mutation/SNP detection.
Methods Mol Biol. 2000;152:159-68. doi: 10.1385/1-59259-068-3:159.
5
One tube mutation detection using sensitive fluorescent dyeing of MutS protected DNA.
Nucleic Acids Res. 2000 Apr 15;28(8):E36. doi: 10.1093/nar/28.8.e36.
7
Measurements of the binding of a large protein using a substrate density-controlled DNA chip.
Anal Chem. 2011 Aug 15;83(16):6368-72. doi: 10.1021/ac201312d. Epub 2011 Jul 20.
8
Mutation detection using immobilized mismatch binding protein (MutS).
Nucleic Acids Res. 1995 Oct 11;23(19):3944-8. doi: 10.1093/nar/23.19.3944.
9
Active microelectronic array system for DNA hybridization, genotyping and pharmacogenomic applications.
Psychiatr Genet. 2002 Dec;12(4):181-92. doi: 10.1097/00041444-200212000-00001.
10
A MutS-based protein chip for detection of DNA mutations.
Anal Chem. 2003 Aug 15;75(16):4113-9. doi: 10.1021/ac020719k.

引用本文的文献

1
MutS protein-based fiber optic particle plasmon resonance biosensor for detecting single nucleotide polymorphisms.
Anal Bioanal Chem. 2021 May;413(12):3329-3337. doi: 10.1007/s00216-021-03271-1. Epub 2021 Mar 13.
2
Electrochemistry of nonconjugated proteins and glycoproteins. Toward sensors for biomedicine and glycomics.
Chem Rev. 2015 Mar 11;115(5):2045-108. doi: 10.1021/cr500279h. Epub 2015 Feb 9.
4
Low density DNA microarray for detection of most frequent TP53 missense point mutations.
BMC Biotechnol. 2005 Feb 15;5:8. doi: 10.1186/1472-6750-5-8.
5
A novel method of identifying genetic mutations using an electrochemical DNA array.
Nucleic Acids Res. 2004 Oct 21;32(18):e141. doi: 10.1093/nar/gnh141.
6
Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray.
Int J Legal Med. 2004 Apr;118(2):75-82. doi: 10.1007/s00414-003-0419-y. Epub 2004 Jan 14.

本文引用的文献

1
Affinity of mismatch-binding protein MutS for heteroduplexes containing different mismatches.
Biochem J. 2001 Mar 15;354(Pt 3):627-33. doi: 10.1042/0264-6021:3540627.
3
An SNP map of human chromosome 22.
Nature. 2000 Sep 28;407(6803):516-20. doi: 10.1038/35035089.
4
An SNP map of the human genome generated by reduced representation shotgun sequencing.
Nature. 2000 Sep 28;407(6803):513-6. doi: 10.1038/35035083.
5
The use of single-nucleotide polymorphism maps in pharmacogenomics.
Nat Biotechnol. 2000 May;18(5):505-8. doi: 10.1038/75360.
6
Anchored multiplex amplification on a microelectronic chip array.
Nat Biotechnol. 2000 Feb;18(2):199-204. doi: 10.1038/72658.
8
Enzymatic methods for mutation scanning.
Genet Anal. 1999 Feb;14(5-6):181-6. doi: 10.1016/s1050-3862(98)00029-1.
9
Resequencing and mutational analysis using oligonucleotide microarrays.
Nat Genet. 1999 Jan;21(1 Suppl):42-7. doi: 10.1038/4469.
10
DNA variation and the future of human genetics.
Nat Biotechnol. 1998 Jan;16(1):33-9. doi: 10.1038/nbt0198-33.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验