The invention relates to an electrochemical immune sensor for phosphating
protein. In the electrochemical immune sensor, a magnetic nanometer-
antibody composition MPs-p53<15>Ab1 is used as an adsorbent to separate the phosphating
protein, a carbon nanometer sphere CNS is used as a carrier,
lead phosphate-apoferritin (LPA) and a phosphating
protein antibody p5315Ab2 are modified on the surface of the CNS, and thus, LPA-p53<15>Ab2-CNS nanometer complexing agent is prepared for detecting
signal amplification. According to the
sandwich immunoassay principle, the content of the phosphating protein to be detected is in proportion to the captured LPA-p5315Ab2-CNS, and the content of lead ions encapsulated in LPA is detected according to a dissolving
volt-
ampere method to measure the concentration of the phosphating protein in a sample. The method has the advantages of simplicity and convenience for operation and simple and efficient separation, and the
advantage that an integral immunologic reaction is finished in an
epoxy (EP) tube; a large number of LPA
signal molecules are introduced by taking the CAN as the carrier, and each LPA molecule contains a large number of Pb<2+>, so the sensitivity of detection is improved; and the dissolved Pb<2+> is used as a detection
signal without adding an
enzyme substrate, so the electrochemical immune sensor is a
reagent-free sensor. In the electrochemical immune sensor for the phosphating protein, the linear concentration range of the phosphating protein
phosphor-p53<15> is from 0.02 to 20 ng mL<-1>, and the
detection limit is 0.01 ng mL<-1>.