mass spectrometry;
matrix-assisted laser desorption/ionization;
MALDI;
single nucleotide polymorphism;
SNP;
genotyping;
high throughput quantification;
halotyping;
D O I:
10.1016/j.clinbiochem.2004.12.005
中图分类号:
R446 [实验室诊断];
R-33 [实验医学、医学实验];
学科分类号:
1001 ;
摘要:
Matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry has become one of the most powerful and widely applied technologies for SNIP scoring and determination of allele frequencies in the post-genome sequencing era. Although different strategies for allele discrimination combined with MALDI were devised, in practice only primer extension methods are nowadays routinely used. This combination enables the rapid, quantitative, and direct detection of several genetic iriarkers simultaneously in a broad variety of biological samples. In the field of molecular diagnostics, MALDI has been applied to the discovery of genetic markers, that are associated with a phenotype like a disease susceptibility or drug response, as well as an alternative means for diagnostic testing of a range of diseases for which the responsible Mutations are already known. It is one of the first techniques with which whole genorne scans based on single nucleotide polymorphisms were carried out. It is equally well Suited for pathogen identification and the detection of emerging mutant strains as well as for the characterization of the genetic identity and quantitative trait loci mapping in farm animals. MALDI can also be used as a detection platform for a range of novel applications that are more demanding than standard SNP genotyping such as mutation/polymorphism discovery, molecular haplotyping, analysis of DNA methylation, and expression profiling. This review gives an introduction to the application of mass spectrometry for DNA analysis, and provides an overview of most studies using SNPs as genetic markers and MAILDI mass spectrometric detection that are related to clinical applications and molecular diagnostics. Further, it aims to show specialized applications that might lead to diagnostic applications in the future. It does not speculate on whether this methodology will ever reach the diagnostic market. (c) 2005 The Canadian Society of Clinical Chemists. All rights reserved.
机构:
IRCCS Fdn Santa Lucia, Prote & Metabon Unit, Rome, ItalyUniv Cattolica Sacro Cuore, Inst Biochem & Clin Biochem, Largo Francesco Vito 1, I-00168 Rome, Italy
Pieroni, Luisa
Ronci, Maurizio
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机构:
IRCCS Fdn Santa Lucia, Prote & Metabon Unit, Rome, Italy
Univ G dAnnunzio, Dept Med Oral & Biotechnol Sci, Chieti, ItalyUniv Cattolica Sacro Cuore, Inst Biochem & Clin Biochem, Largo Francesco Vito 1, I-00168 Rome, Italy
Ronci, Maurizio
Putignani, Lorenza
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机构:
Bambino Gesu Pediat Hosp, IRCCS, Unit Parasitol, Rome, Italy
Bambino Gesu Pediat Hosp, Unit Human Microbiome, IRCCS, Rome, ItalyUniv Cattolica Sacro Cuore, Inst Biochem & Clin Biochem, Largo Francesco Vito 1, I-00168 Rome, Italy
Putignani, Lorenza
Roncada, Paola
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机构:
Magna Graecia Univ Catanzaro, Dipartimento Sci Salute, Catanzaro, ItalyUniv Cattolica Sacro Cuore, Inst Biochem & Clin Biochem, Largo Francesco Vito 1, I-00168 Rome, Italy
机构:
Univ Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, England
Ye, S
Dhillon, S
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Univ Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, England
Dhillon, S
Ke, XY
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Univ Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, England
Ke, XY
Collins, AR
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Univ Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, England
Collins, AR
Day, INM
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Univ Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, EnglandUniv Southampton, Human Genet Res Div, Southampton SO16 6YD, Hants, England