# US 12,110,542 B2 · Isothermal amplification

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- Number: US 12,110,542 B2
- Document ID: US12110542B2
- Status: Granted
- Kind: B2
- Application number: 17/472,300
- Filed: 2021-09-10
- Published: 2022-03-17
- Granted: 2024-10-08
- Earliest claimed: 2020-09-10
- Assignees: University of Connecticut
- Applicants: University of Connecticut
- Inventors: Changchun Liu; Xiong Ding
- Web page: https://patentgrep.com/patent/US12110542B2

## CPC

- C12Q 1/6844: Nucleic acid amplification reactions
- C12Q 1/6855: Ligating adaptors
- C12Q: MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS (immunoassay G01N33/53); COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES

## Abstract

Disclosed herein are “dual-priming” isothermal amplification method (including “self-priming” and “pairing-priming” strand extension, termed “DAMP”) for rapid nucleic acid detection.

## Claims

### Claim 1

A method of amplifying a target nucleic acid, comprising contacting a nucleic acid sample suspected of containing the target nucleic acid with six primers and a DNA polymerase with strand displacement activity, wherein
the target nucleic acid comprises from 5′ to 3′, an F3 site, an F2 site, an F1 site, an R1 site, an R2 site, and an R3 site, and the complement to the target nucleic acid comprises, from 3′ to 5′, an F3c site, an F2c site, an F1c site, an R1c site, an R2c site, and an R3c site, and
the six primers comprise
a forward outer primer (FO) complementary to the F3c site,
a reverse outer primer (RO) complementary to the R3 site,
a forward inner primer (FI) comprising the F1c and F2 sites,
a reverse inner primer (RI) comprising the R1 and R2c sites,
a forward reverse pairing-competition primer (FC) complementary to the F1 site, and
a reverse pairing-competition primer (RC) complementary to the R1c site,
wherein the forward outer primer (FO), the reverse outer primer (RO), the forward reverse pairing-competition primer (FC), and the reverse pairing-competition primer (RC) are single site primers, and the forward inner primer (FI) and the reverse inner primer (RI) are double site primers; and
amplifying the target nucleic acid with the DNA polymerase, wherein amplifying comprises
producing a first basic structure comprising from 5′ to 3′, the R1 site, the R2c site, the R1c site, the F1c site, the F2c site, and the F1 site, wherein producing comprises
(a) synthesizing DNA from (1) the forward outer primer (FO) annealing to the F3c site with the DNA polymerase and (2) the F2 region of the forward inner primer (FI) annealing to the F2c site with the DNA polymerase, wherein the strand elongated from the forward inner primer (FI) is displaced and released by the extension from the forward outer primer (FO), and
(b) synthesizing DNA (1) with the DNA polymerase from the reverse outer primer (RO) annealing to the R3 site and (2) with the DNA polymerase from the R2c region of the reverse inner primer (RI) annealing the R2 site of the released nucleic acid strand, wherein the strand elongated from the reverse inner primer (RI) is displaced and released by the extension from the reverse outer primer (RO), thereby producing the first basic structure, and
cyclically amplifying the first basic structure by contacting the first basic structure with the DNA polymerase, the forward inner primer (F1), the reverse pairing-competition primer (RC), the forward reverse pairing-competition primer (FC), and the reverse inner primer (RI) to provide amplified target nucleic acid.

### Claim 2 (depends on 1)

The method of claim 1, wherein
the distance from the first nucleotide of the F2 site to the first nucleotide of the FI site in the target nucleic acid sequence is less than 40 nucleotides,
the distance from the first nucleotide of the R2c site to the first nucleotide of the R1c site in the complement to the target nucleic acid sequence is less than 40 nucleotides, or
a combination thereof.

### Claim 3 (depends on 1)

The method of claim 1, wherein the cyclic amplifying comprises
(A) synthesizing DNA (1) with the DNA polymerase from the annealing of the FI site of the first basic structure and the F1c site of the first basic structure and (2) with the DNA polymerase from the F2 region of the forward inner primer (FI) annealing to the F2c site of the first basic structure,
(B) synthesizing DNA with the DNA polymerase from the forward reverse pairing-competition primer (FC) annealing to the FI site of the first basic structure with the DNA polymerase, thereby producing a duplex basic structure comprising a first basic structure and a second basic structure, the second basic structure from 5′ to 3′, the F1c site, the F2 site, the F1 site, the RI site, the F2 site, and the R1c site, or
(C) synthesizing DNA (1) with the DNA polymerase from the annealing of the F2 region of the forward inner primer (FI) annealing to the F2c site of the first basic structure and (2) with the DNA polymerase from the forward reverse pairing-competition primer (FC) annealing to the F1 site of the first basic structure, wherein the strand elongated from the forward inner primer (FI) is displaced and released by the extension from the forward reverse pairing-competition primer (FC), thereby producing a duplex basic structure and a second basic structure, or
(D) a combination thereof.

### Claim 4 (depends on 3)

The method of claim 3, wherein the cyclic amplifying further comprises
(1) synthesizing DNA (i) with the DNA polymerase from the annealing of the F2 region of the forward inner primer (FI) annealing to the F2c site of the first basic structure of the duplex basic structure and (ii) with the DNA polymerase from the forward reverse pairing-competition primer (FC) annealing to the FI site of the first basic structure of the duplex basic structure of (B) or (C), wherein the strand elongated from the forward inner primer (FI) is displaced and released by the extension from the forward reverse pairing-competition primer (FC), thereby producing a duplex basic structure and a second basic structure,
(2) synthesizing DNA (i) with the DNA polymerase from the annealing of the R2c region of the reverse inner primer (RI) annealing to the R2 site of the second basic structure or the second basic structure of the basic duplex structure from (B) or (C) and (ii) with the DNA polymerase from the reverse pairing-competition primer (RC) annealing to the R1C site of the second basic structure or the second basic structure of the basic duplex structure from (B) or (C), wherein the strand elongated from the reverse inner primer (RI) is displaced and released by the extension from the reverse pairing-competition primer (RC), thereby a the duplex basic structure and a first basic structure,
(3) synthesizing DNA (i) with the DNA polymerase from the R2c region of the reverse inner primer (RI) annealing to the R2 site of the product of (A) and (ii) with the DNA polymerase from the reverse pairing-competition primer (RC) annealing to the R1C site of the product of (A), wherein the strand elongated from the reverse inner primer (RI) is displaced and released by the extension from the reverse pairing-competition primer (RC), or
(4) a combination thereof.

### Claim 5 (depends on 1)

The method of claim 1, wherein the F1c site and the F2 site of the forward inner primer (FI) are separated by a TTTT spacer.

### Claim 6 (depends on 1)

The method of claim 1, wherein the R1 site and the R2c site of the reverse inner primer (RI) are separated by a TTTT spacer.