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   <subfield code="a">Chemiluminescence assay for angiogenin using a signal amplification technology based on the cleavage of nicking endonucleases</subfield>
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   <subfield code="c">[Yunhua He, Feng Nie]</subfield>
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   <subfield code="a">Traditional protein assays based on the recognition of a target molecule by signal probe in a 1:1 stoichiometric ratio are limitated in sensitivity because one target molecule causes the production of a single signal probe only. We report on a novel approach for the determination of angiogenin (Ang). It is based on the cleavage of the Nb.Bsm I (nicking endonucleases) and an associated signal amplification technology using Au nanoparticles (AuNPs) as labels. The signal is amplified via Ang-aptamer recognition and after cleavage of the Nb.Bsm I, upon which one Ang can produce several chemiluminescent signal probes based on AuNPs. This results in a significant increase in the limit of detection of Ang (0.2pmol L−1). The method also is highly selective. Ang was determined in serum samples, and the results confirmed the reliability and practicality of the protocol. Figure A novel approach for the determination of angiogenin (Ang) was developed based on the cleavage of the Nb.Bsm I and an associated signal amplification technology using Au nanoparticles (AuNPs) as labels. This results in a significant increase in the limit of detection of Ang (0.2pmol L−1)</subfield>
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