The 60 nm gold nanoparticles improve qPCR amplification efficiency through specific palindromic sequences (GGATCC or ACCGGT) in primers
Polymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) ca...
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Published in | Biochimica et biophysica acta. General subjects Vol. 1868; no. 4; p. 130560 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.04.2024
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Abstract | Polymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) can be used to improve the sensitivity and amplification efficiency of PCR. Here, we found that 60 nm gold nanoparticles with a positive charge (60 nm- Au+) can enhance the amplification efficiency of qPCR.
Mouse DNA was extracted by the alkaline lysis method. Primer 5.0 software was used to design primers and mutation primers, and the DNA fragments were obtained by the method of synthesizing plasmids. The qPCR was applied to amplify target gene fragments.
The amplification efficiency of qPCR was improved by about 1.828 times in the experimental group with 60 nm- Au+ compared with the control group without 60 nm- Au+. The primer pair contains a specific palindromic sequence (GGATCC or ACCGGT). And 60 nm Au+ did not enhance the amplification efficiency of qPCR when the above primer was mutated.
The primers contain special palindrome sequences (GGATCC or ACCGGT) with 60 nm- Au+ can enhance the amplification efficiency of qPCR. Therefore, it suggests a more in-depth understanding of the mechanism and function of gold nanoparticles and primer sequences. This study has presented some implications for gold nanoparticles application in the development of qPCR technology.
•Now, it is controversial whether AuNPs promote PCR amplification efficiency.•60 nm- Au+ promotes the amplification efficiency of qPCR with primers containing palindromic sequences.•Mutating palindromic sequences in primers did not again improve the amplification efficiency of qPCR.•It suggested the AuNPs and some special DNA primers are associated with the qPCR amplification system. |
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AbstractList | Polymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) can be used to improve the sensitivity and amplification efficiency of PCR. Here, we found that 60 nm gold nanoparticles with a positive charge (60 nm- Au+) can enhance the amplification efficiency of qPCR.BACKGROUNDPolymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) can be used to improve the sensitivity and amplification efficiency of PCR. Here, we found that 60 nm gold nanoparticles with a positive charge (60 nm- Au+) can enhance the amplification efficiency of qPCR.Mouse DNA was extracted by the alkaline lysis method. Primer 5.0 software was used to design primers and mutation primers, and the DNA fragments were obtained by the method of synthesizing plasmids. The qPCR was applied to amplify target gene fragments.METHODSMouse DNA was extracted by the alkaline lysis method. Primer 5.0 software was used to design primers and mutation primers, and the DNA fragments were obtained by the method of synthesizing plasmids. The qPCR was applied to amplify target gene fragments.The amplification efficiency of qPCR was improved by about 1.828 times in the experimental group with 60 nm- Au+ compared with the control group without 60 nm- Au+. The primer pair contains a specific palindromic sequence (GGATCC or ACCGGT). And 60 nm Au+ did not enhance the amplification efficiency of qPCR when the above primer was mutated.RESULTSThe amplification efficiency of qPCR was improved by about 1.828 times in the experimental group with 60 nm- Au+ compared with the control group without 60 nm- Au+. The primer pair contains a specific palindromic sequence (GGATCC or ACCGGT). And 60 nm Au+ did not enhance the amplification efficiency of qPCR when the above primer was mutated.The primers contain special palindrome sequences (GGATCC or ACCGGT) with 60 nm- Au+ can enhance the amplification efficiency of qPCR. Therefore, it suggests a more in-depth understanding of the mechanism and function of gold nanoparticles and primer sequences. This study has presented some implications for gold nanoparticles application in the development of qPCR technology.CONCLUSIONSThe primers contain special palindrome sequences (GGATCC or ACCGGT) with 60 nm- Au+ can enhance the amplification efficiency of qPCR. Therefore, it suggests a more in-depth understanding of the mechanism and function of gold nanoparticles and primer sequences. This study has presented some implications for gold nanoparticles application in the development of qPCR technology. Polymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) can be used to improve the sensitivity and amplification efficiency of PCR. Here, we found that 60 nm gold nanoparticles with a positive charge (60 nm- Au ) can enhance the amplification efficiency of qPCR. Mouse DNA was extracted by the alkaline lysis method. Primer 5.0 software was used to design primers and mutation primers, and the DNA fragments were obtained by the method of synthesizing plasmids. The qPCR was applied to amplify target gene fragments. The amplification efficiency of qPCR was improved by about 1.828 times in the experimental group with 60 nm- Au compared with the control group without 60 nm- Au . The primer pair contains a specific palindromic sequence (GGATCC or ACCGGT). And 60 nm Au did not enhance the amplification efficiency of qPCR when the above primer was mutated. The primers contain special palindrome sequences (GGATCC or ACCGGT) with 60 nm- Au can enhance the amplification efficiency of qPCR. Therefore, it suggests a more in-depth understanding of the mechanism and function of gold nanoparticles and primer sequences. This study has presented some implications for gold nanoparticles application in the development of qPCR technology. Polymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) can be used to improve the sensitivity and amplification efficiency of PCR. Here, we found that 60 nm gold nanoparticles with a positive charge (60 nm- Au+) can enhance the amplification efficiency of qPCR. Mouse DNA was extracted by the alkaline lysis method. Primer 5.0 software was used to design primers and mutation primers, and the DNA fragments were obtained by the method of synthesizing plasmids. The qPCR was applied to amplify target gene fragments. The amplification efficiency of qPCR was improved by about 1.828 times in the experimental group with 60 nm- Au+ compared with the control group without 60 nm- Au+. The primer pair contains a specific palindromic sequence (GGATCC or ACCGGT). And 60 nm Au+ did not enhance the amplification efficiency of qPCR when the above primer was mutated. The primers contain special palindrome sequences (GGATCC or ACCGGT) with 60 nm- Au+ can enhance the amplification efficiency of qPCR. Therefore, it suggests a more in-depth understanding of the mechanism and function of gold nanoparticles and primer sequences. This study has presented some implications for gold nanoparticles application in the development of qPCR technology. •Now, it is controversial whether AuNPs promote PCR amplification efficiency.•60 nm- Au+ promotes the amplification efficiency of qPCR with primers containing palindromic sequences.•Mutating palindromic sequences in primers did not again improve the amplification efficiency of qPCR.•It suggested the AuNPs and some special DNA primers are associated with the qPCR amplification system. Polymerase chain reaction (PCR) technology and quantitative real-time PCR (qPCR) technology are widely used in clinical diagnosis and research, but amplification efficiency and sensitivity are still key problems for researchers. An increasing number of reports show that gold nanoparticles (AuNPs) can be used to improve the sensitivity and amplification efficiency of PCR. Here, we found that 60 nm gold nanoparticles with a positive charge (60 nm- Au⁺) can enhance the amplification efficiency of qPCR. Mouse DNA wsa extracted by the alkaline lysis method. Primer 5.0 software was used to design primers and mutation primers, and the DNA fragments were obtained by the method of synthesizing plasmids. The qPCR was applied to amplify target gene fragments. The amplification efficiency of qPCR was improved by about 1.828 times in the experimental group with 60 nm- Au⁺ compared with the control group without 60 nm- Au⁺. The primer pair contains a specific palindromic sequence (GGATCC or ACCGGT). And 60 nm Au⁺ did not enhance the amplification efficiency of qPCR when the above primer was mutated. The primers contain special palindrome sequences (GGATCC or ACCGGT) with 60 nm- Au⁺ can enhance the amplification efficiency of qPCR. Therefore, it suggests a more in-depth understanding of the mechanism and function of gold nanoparticles and primers sequences. This study has presented some implications for gold nanoparticles application in the development of qPCR technology. |
ArticleNumber | 130560 |
Author | Li, Jiangchao Zeng, Ruyu Meng, Xiuqiong Li, Erhua Du, Zhiqun Ma, Hongliang |
Author_xml | – sequence: 1 givenname: Ruyu surname: Zeng fullname: Zeng, Ruyu organization: The Department of Pathology and Pathophysiology, School of Basic Medical Sciences, Guangdong Pharmaceutical University, Guangzhou, 510006, China – sequence: 2 givenname: Zhiqun surname: Du fullname: Du, Zhiqun organization: The Department of Pathology, Dongyang People's Hospital, Zhejiang, China – sequence: 3 givenname: Hongliang surname: Ma fullname: Ma, Hongliang organization: The Department of Pathology and Pathophysiology, School of Basic Medical Sciences, Guangdong Pharmaceutical University, Guangzhou, 510006, China – sequence: 4 givenname: Xiuqiong surname: Meng fullname: Meng, Xiuqiong organization: The Department of Pathology and Pathophysiology, School of Basic Medical Sciences, Guangdong Pharmaceutical University, Guangzhou, 510006, China – sequence: 5 givenname: Erhua surname: Li fullname: Li, Erhua organization: Guangzhou BDS Biological Technology Co., Ltd. Guangzhou, China – sequence: 6 givenname: Jiangchao surname: Li fullname: Li, Jiangchao email: lijiangchao@gdpu.edu.cn organization: The Department of Pathology and Pathophysiology, School of Basic Medical Sciences, Guangdong Pharmaceutical University, Guangzhou, 510006, China |
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Keywords | SSB DMSO Palindrome sequence Primes UV–VIS CNTs qPCR 60 nm- Au SEM TMAC TEM qRT–PCR Gold nanoparticle PCR |
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Title | The 60 nm gold nanoparticles improve qPCR amplification efficiency through specific palindromic sequences (GGATCC or ACCGGT) in primers |
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