Macromolecular environment control in specific receptor assays

Claim 1

An assay method for determining the presence in a sample of an analyte, wherein the ligand with its homologous antiligand define a specific binding pair, wherein said method employs (1) a medium comprised of an aqueous buffered continuous phase at a pH in the range of about 6.5 to 9.5 and a discontinuous solid phase of dispersable porous discrete particles to which is conjugated one of the members of said specific binding pair and the enzyme β-galactosidase to provide a particle conjugate and (2) a signal producing system capable of producing a measurable signal and having a second enzyme alkaline phosphatase conjugated to a member of said specific binding pair to provide a signal label conjugate, wherein said first and second enzymes with 4-methylumbelliferyl-β-D-galactopyranoside-6-phosphate define said signal producing system, said particle conjugate defining an environment which affects the production of a fluorescent signal differently from said aqueous medium, so that said measurable signal varies in relation to the partitioning of said signal label conjugate between said particles and said aqueous medium, said partitioning being related to the amount of analyte in said medium, said method comprising: combining in said aqueous medium, (a) said sample; (b) said particle conjugate substantially uniformly dispersed in said aqueous medium; (c) said signal label conjugate; (d) the homologous member of said specific binding pair, when said analyte, particle conjugate and signal label conjugate have the same member; and (e) 4-methylumbelliferyl-β-D-galactopyranoside-6-phosphate, whereby said signal label conjugate will be partitioned between said aqueous medium and said particle conjugate to a degree dependent upon the amount of ligand in said sample; and determining the level of said fluorescent signal as compared to an assay medium having a known amount of analyte.