Self-priming hairpin-mediated isothermal amplification
The present invention relates to a self-priming hairpin-mediated isothermal amplification (SP-HAMP) and, more specifically, to a hairpin probe having a self-priming structure, which is for detecting a target nucleic acid and can be used in the nucleic acid isothermal amplification, and to a method for detecting a target nucleic acid by using same. The SP-HAMP technique according to the present invention is convenient due to no need of a separate primer with a complicated design required in existing LAMP technology, has improved efficiency of detection compared with existing LAMP reactions, and can detect DNA as well as RNA as a target nucleic acid, and therefore the technique according to the present invention can be applied in a wider variety of fields.
1 . A hairpin probe comprising the following components and having a self-priming structure for detecting target nucleic acids:
(i) a PS1 region disposed at a 5′ end of the hairpin probe, the PS1 region modified with phosphorothioate DNA, the PS1 region having a sequence complementary to a PS1′ region:
(ii) an X region linked to the PS1 region, the X region disposed on a stem of the hairpin probe including a sequence complementary to a target nucleic acid;
(iii) the PS1′ region disposed in a loop of the hairpin probe, the PS1′ region linked to the X region, the PS1′ region having a sequence complementary to the target nucleic acid following the sequence complementary to the target nucleic acid of the X region, the PS1′ region modified with phosphorothioate DNA;
(iv) an L region linked to the PS1′ region, the L region having a sequence complementary to the target nucleic acid following the sequence complementary to the target nucleic acid of the PS1′ region, the L region disposed in the loop of the hairpin probe;
(v) an a region of a self-priming hairpin, linked to the L region, the a region including a sequence complementary to a part of the X region to form a stem of the hairpin probe;
(vi) a b region of the self-priming hairpin, linked to the a region of the self-priming hairpin, the b region including a sequence complementary to a part of the X region to form the stem of the hairpin probe; and
(vii) an a′ region of the self-priming hairpin, disposed at a 3′ end of the hairpin probe, the a′ region linked to the b region of the self-priming hairpin, the a′ region including a sequence complementary to the a region of the self-priming hairpin.
2 . A method for detecting a target nucleic acid comprising:
(a) reacting a composition containing a sample containing the target nucleic acid, the hairpin probe having the self-priming structure according to claim 1 , a nucleic acid polymerase, and dNTPs to obtain an intermediate product including the hairpin probe extended by the self-priming structure; and
(b) analyzing the produced hairpin probe intermediate product to detect the target nucleic acid.
3 . A composition for detecting a target nucleic acid comprising:
a sample containing the target nucleic acid;
the hairpin probe having the self-priming structure according to claim 1 ;
a nucleic acid polymerase; and
dNTPs.
4 . A kit for detecting a target nucleic acid comprising:
the hairpin probe having the self-priming structure according to claim 1 .