Enhanced recognition of cystic fibrosis W1282X DNA point mutation by chiral peptide nucleic acid probes by a surface plasmon resonance biosensor

被引:58
作者
Corradini, R
Feriotto, G
Sforza, S
Marchelli, R
Gambari, R
机构
[1] Univ Parma, Dipartimento Chim Organ & Ind, I-43100 Parma, Italy
[2] Univ Ferrara, Ctr Biotecnol, I-44100 Ferrara, Italy
[3] Univ Ferrara, Dipartimento Biochim & Biol Mol, I-44100 Ferrara, Italy
关键词
peptide nucleic acids; chirality; Biacore; surface plasmon resonance; cystic fibrosis; point mutation;
D O I
10.1002/jmr.646
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peptide nucleic acids (PNAs) containing an insert of three chiral monomers based on D-lysine ('chiral box') were synthesized and used as probes in Biospecific Interaction Analysis (BIA) for the recognition of DNA containing the W1282X point mutation of the cystic fibrosis gene. Hybridization experiments carried out in solution showed enhanced mismatch recognition when compared with the analogous achiral PNAs and oligonucleotides. The signal intensity was lower, but the selectivity of the Biacore response was found to be much higher than that observed with achiral PNAs. The newly designed chiral PNA probes were also found to hybridize with a 1:1 mixture of normal (N-W1282X) and mutated (M-W1282X) DNA oligomers immobilized on the biosensor, thus allowing discrimination not only between a normal and a mutated sequence (healthy/homozygous), but also between homo- and heterozygous individuals. These results suggest that 'chiral box' PNAs are potential powerful tools for the analysis of single point mutations of biological/biomedical relevance. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:76 / 84
页数:9
相关论文
共 41 条
  • [1] Synthesis of a stable and specific surface plasmon resonance biosensor surface employing covalently immobilized peptide nucleic acids
    Burgener, M
    Sänger, M
    Candrian, U
    [J]. BIOCONJUGATE CHEMISTRY, 2000, 11 (06) : 749 - 754
  • [2] Effects in live cells of a c-myc anti-gene PNA linked to a nuclear localization signal
    Cutrona, G
    Carpaneto, EM
    Ulivi, M
    Roncella, S
    Landt, O
    Ferrarini, M
    Boffa, LC
    [J]. NATURE BIOTECHNOLOGY, 2000, 18 (03) : 300 - 303
  • [3] Inhibition of RNA polymerase III elongation by a T10 peptide nucleic acid
    Dieci, G
    Corradini, R
    Sforza, S
    Marchelli, R
    Ottonello, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (08) : 5720 - 5725
  • [4] Dueholm KL, 1997, NEW J CHEM, V21, P19
  • [5] PNA HYBRIDIZES TO COMPLEMENTARY OLIGONUCLEOTIDES OBEYING THE WATSON-CRICK HYDROGEN-BONDING RULES
    EGHOLM, M
    BUCHARDT, O
    CHRISTENSEN, L
    BEHRENS, C
    FREIER, SM
    DRIVER, DA
    BERG, RH
    KIM, SK
    NORDEN, B
    NIELSEN, PE
    [J]. NATURE, 1993, 365 (6446) : 566 - 568
  • [6] PEPTIDE NUCLEIC-ACIDS (PNA) - OLIGONUCLEOTIDE ANALOGS WITH AN ACHIRAL PEPTIDE BACKBONE
    EGHOLM, M
    BUCHARDT, O
    NIELSEN, PE
    BERG, RH
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (05) : 1895 - 1897
  • [7] Feriotto G, 1999, HUM MUTAT, V13, P390, DOI 10.1002/(SICI)1098-1004(1999)13:5<390::AID-HUMU8>3.0.CO
  • [8] 2-1
  • [9] Peptide nucleic acids and biosensor technology for real-time detection of the cystic fibrosis W1282X mutation by surface plasmon resonance
    Feriotto, G
    Corradini, R
    Sforza, S
    Bianchi, N
    Mischiati, C
    Marchelli, R
    Gambari, R
    [J]. LABORATORY INVESTIGATION, 2001, 81 (10) : 1415 - 1427
  • [10] Peptide nucleic acids: Analogs and derivatives
    Ganesh, KN
    Nielsen, PE
    [J]. CURRENT ORGANIC CHEMISTRY, 2000, 4 (09) : 931 - 943