Method for HLA typing

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S091100, C435S091200

Reexamination Certificate

active

07820377

ABSTRACT:
A method for the identification of DNA sequence elements in complex and highly variable sequences is described. The method consists of identifying a short sequence element of several DNA bases (2-6 bases) at a given position in the genome simultaneously on all parental alleles. The method allows differentiating mini-haplotypes on different alleles in one analysis. The method consists of carrying out an enzymatic primer extension reaction with a combination of extension primers (pool of primers) and analysing the products by mass spectrometry. The pool of primers is assembled in such a way that the primer extension product allows unambiguous identification of both the primer of the pool that was extended and the base that was added. The method is of great utility for DNA sequences harbouring many SNPs close to each other with many possible haplotypes. Such sequences are known in the Major Histocompatibility Complex (MHC). This method is particularly well suited for DNA-based HLA typing and in combination with a suitable selection of sites tested, it is superior in ease of operation to conventional HLA typing methods. We have identified sets of these assays for HLA-A, HLA-B, and HLA-DRB 1 that allow unambiguous four-digit HLA of each of these genes with between 11 and 28 queried markers.

REFERENCES:
patent: 5451512 (1995-09-01), Apple et al.
patent: WO 00/65088 (2000-11-01), None
patent: WO 02/08462 (2002-01-01), None
patent: WO 02/18659 (2002-03-01), None
Pastinen et al., “Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation,”Clinical Chemistry, American Association for Clinical Chemistry, vol. 42, No. 9, 1996, pp. 1391-1397.
Worrall et al., “Allele-specific HLA-DR typing by mass spectrometry: an alternative to hybridization-based typing methods,”Analytical Chemistry, Nov. 1, 2000, vol. 72, No. 21, pp. 5233-5238.
Leushner et al., “Automated mass spectroscopic platform for high throughput DR Beta typing,”Human Immunology, vol. 61, No. Supplement 2, 2000, p. S126.
Tost et al., “Genotyping single nucleotide polymorphisms by mass spectrometry,”Mass Spectrometry Reviews, vol. 21, No. 6, Nov. 2002, pp. 388-418.
Tost et al., “Molecular haplotyping at high throughput,”Nucleic Acids Research, Oct. 1, 2002, vol. 30, No. 19, p. e96.
Sauer et al., “Extension of the good assay for genotyping single nucleotide polymorphisms by matrix-assisted laser desorption/ionization mass spectrometry,”Rapid Communications in Mass Spectrometry, vol. 17, No. 12, May 9, 2003, pp. 1265-1272.
Sauer et al., “Genotyping single-nucleotide polymorphisms by matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry,”Journal of Chromatography B, Analytical Technologies in the Biomedical and Life Sciences, Dec. 25, 2002, vol. 782, No. 1-2, pp. 73-87.
Rozemuller, “Reference panels for sequence based typing: Selection criteria for HLA-A and HLA-B,” 2000, retrieved from the Internet: URL:http://wwww.ihwg.org/tmanual/TMcontents.htm, retrieved on Jul. 5, 2004.
Ross et al., “Discrimination of Single-Nucleotide Polymorphisms in Human DNA Using Peptide Nucleic Acid Probes Detected by MALDI-TOF Mass Spectrometry,”Anal. Chem., vol. 69, pp. 4197-4202, 1997.
Ross et al., “High level multiplex genotyping by MALDI-TOF mass spectrometry,”Nature Biotechnology, vol. 16, pp. 1347-1351, Dec. 1998.
Robinson et al., “Exon Identities and Ambiguous Typing Combinations,”Anthony Nolan Research Institute, Oct. 2003.
Petersdorf et al., “Tissue typing in support of unrelated hematopoietic cell transportation,”Tissue Antigens, vol. 61, pp. 1-11, 2003.
Liu et al., “Rapid Screening of Genetic Polymorphisms Using Buccal Cell DNA with Detection by Matrix-assisted Laser Desorption/Ionization Mass Spectrometry,”Rapid Communications in Mass Spectrometry, vol. 9, pp. 735-743, 1995.
Little et al., “Detection of RET proto-oncogene codon 634 mutations using mass spectrometry,”J. Mol. Med., vol. 73, pp. 743-750, 1997.
Haff et al., “Single-Nucleotide Polymorphism Identification Assays Using a Thermostable DNA Polymerase and Delayed Extraction MALDI-TOFF Mass?Spectrometry,”Genome Research, vol. 7, pp. 378-388, 1997.
Griffin et al., “Genetic analysis by peptide nucleic acid affinity MALDI-TOF mass spectrometry,”Nature Biotechnology, vol. 15, pp. 1368-1372, Dec. 1997.
Fei et al., “MALDI-TOF mass spectrometric typing of single nucleotide polymorphisms with mass-tagged.ddNTPs,”Nucleic Acids Research, vol. 26, No. 11, pp. 2827-2828, 1998.
Ch'Ang et al., “Detection of ΔF508 Mutation of the Cystic Fibrosis Gene by Matrix-assisted Laser Desorption/Ionization Mass Spectrometry,”Rapid Communications in Mass Spectrometry, vol. 9, pp. 772-774, 1995.
Karas et al., “Laser Desorption Ionization of Proteins with Molecular Masses Exceeing 10,000 Daltons,”Anal. Chem., vol. 60, pp. 2299-2301, 1988.
Tost et al., “Genotyping Single Nucleotide Polymorphisms by Mass Spectrometry,”Mass Spectrometry Reviews, vol. 21, pp. 388-418, 2002.
International Search Report issued on Jul. 11, 2005 for application No. PCT/IB2004/004115.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Method for HLA typing does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Method for HLA typing, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method for HLA typing will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4198700

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.