US4097149A
Expired / Lapsed
US
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Quantitative protein analysis by immunodiffusion
Assignee: Individual
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Filing: 1975-02-03
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Granted: 1978-06-27
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Expires: 1995-02-03
Abstract
Abstract Methods are described by which immunochemical procedures such as immunodiffusion and immunoelectrophoresis can be used to provide quantitative measurement of the concentration of individual proteins in fluids such as serum, spinal fluid, tissue extracts and the like. That is accomplished typically by making quantitative optical measurements of the zones of precipitation which are produced, in parallel with those of standard preparations containing known concentrations of the proteins to be determined; deriving from the measurements of the precipitation zones selected parameters; and comparing the selected values of the experimental and reference preparations. The zone measurements are preferably made by scanning the plates electronically, with suitable arithmetic manipulation of the resulting video values at a plurality of selected positions for each zone.
Inventors
- 👤 Frederick J. Aladjem
- 👤 Padmasini K. Ayengar
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-24 04:51
CPC Classifications
G; G01; G01N; G01N27/00; G01N27/26; G01N27/416; G01N27/447; G01N27/44704; G01N27/44717; G01N27/44721; Y; Y10; Y10S; Y10S436/00; Y10S436/805
Claims Analysis
Total Claims: 18
Claim 1
Independent Claim
254 words
Method of obtaining a quantitative measurement of the concentration of a protein in an antigen sample which has been subjected to immunoelectrophoresis including the steps of producing selective protein migration by electrophoresis in one dimension in a thin layer of supporting medium, and subjecting the antigen sample after said migration to immunodiffusion with an antibody source containing an antibody specific to said protein, the protein and antibody diffusing into reactive contact in another dimension through an area of said medium layer intially free of both antigen and antibody and reacting to form an elongated precipitation zone; said method comprising scanning the zone by optical means under dark field illumination, at a selected time following initiation of said diffusion, along a plurality of generally parallel mutually spaced scan paths which cross the zone transversely to develop electrical intensity signals representing the intensity of the scattered light at a series of positions on each scan path, said positions being distributed partly within the zone and partly outside the zone, deriving from said intensity signals for a plurality of said positions within the zone an electrical sum signal representing the sum of the effective excess of each of the intensities within the zone over intensities outside the zone, and comparing the resulting sum signal with a set of reference sum signals derived from corresponding measurements of reference zones produced by equivalent immunoelectrophoresis of a plurality of reference antigen solutions containing respective known concentrations of said protein, thereby providing a quantitative measure of the concentration of said protein.
Claim 2
Dependent Claim
254 words
Method of obtaining a quantitative measurement of the concentration of a protein in an antigen sample which has been subjected to immunoelectrophoresis including the steps of producing selective protein migration by electrophoresis in one dimension in a thin layer of supporting medium, and subjecting the antigen sample after said migration to immunodiffusion with an antibody source containing an antibody specific to said protein, the protein and antibody diffusing into reactive contact in another dimension through an area of said medium layer intially free of both antigen and antibody and reacting to form an elongated precipitation zone; said method comprising scanning the zone by optical means under dark field illumination, at a selected time following initiation of said diffusion, along a plurality of generally parallel mutually spaced scan paths which cross the zone transversely to develop electrical intensity signals representing the intensity of the scattered light at a series of positions on each scan path, said positions being distributed partly within the zone and partly outside the zone, deriving from said intensity signals for a plurality of said positions within the zone an electrical sum signal representing the sum of the effective excess of each of the intensities within the zone over intensities outside the zone, and comparing the resulting sum signal with a set of reference sum signals derived from corresponding measurements of reference zones produced by equivalent immunoelectrophoresis of a plurality of reference antigen solutions containing respective known concentrations of said protein, thereby providing a quantitative measure of the concentration of said protein.
Claim 3
Dependent Claim
56 words
Method according to claim 1 wherein said step of scanning the zone to develop electrical intensity signals is repeated at a series of definite times as the individual zone develops, and the steps of deriving and comparing sum signals are carried out for each of said times, using corresponding respective development times of said reference zones.
Claim 4
Dependent Claim
77 words
Method according to claim 2 including extrapolating said electrical sum signals back in time to zero value to determine a time of initial appearance of the zone, and comparing the resulting value of the time of initial appearance of the zone with a set of reference values derived by similar extrapolation to zero of corresponding reference sum signals representing a similar series of definite times, thereby providing a further quantitative measure of the concentration of said protein.
Claim 5
Dependent Claim
27 words
Method according to claim 1 wherein said step of scanning the zone to develop electrical intensity signals is carried out after said immunodiffusion has reached substantial equilibrium.
Claim 6
Dependent Claim
68 words
Method according to claim 1 wherein said step of scanning the zone to develop electrical signals comprises forming an optical image of the zone at the image surface of a video camera tube, representing the intensity of the image at each said position as a digital representation, and storing in a memory associated with a digital computer the digital representations and digital addresses identifying the respective image positions.
Claim 7
Dependent Claim
108 words
Method according to claim 1 wherein said scan paths include at least one path spaced beyond each end of the zone, and said method includes deriving electronically as a measure of the length of the zone an electronic signal representing the separation of the two outermost scan paths that include at least one said position within the zone for which said intensity signal has a distinct excess over intensity signals at positions outside the zone, and comparing the resulting zone length signal with the set of reference zone length signals derived correspondingly from said reference zones, thereby providing a further quantitative measure of the concentration of said protein.
Claim 8
Dependent Claim
98 words
Method according to claim 6 wherein a plurality of equivalent antigen samples and a plurality of equivalent samples of each said reference solutions are subjected to said immunoelectrophoresis and to said subsequent steps of measurement and analysis, said method including the steps of electronically computing the respective probable experimental errors of said quantitative measures of the concentration of said protein obtained from said sum signals and obtained from said zone length signals, and electronically comparing the difference of said quantitative measures with a summation of said experimental errors to detect presence of an abnormal condition of said protein.
Claim 9
Dependent Claim
93 words
Method according to claim 1 wherein said positions at which light intensity signals are developed include at least one position in said zone on one side thereof and in a region of overlaps with another zone, and said step of scanning the zone to develop intensity signals includes developing an electrical intensity signal at a second position which is correspondingly placed on the other side of the first said zone and in a region free of overalap, and employing the so developed intensity signal as the zone intensity signal for said one position.
Claim 10
Dependent Claim
146 words
Method according to claim 1 wherein said positions at which intensity signals are developed include at least one position which is in said zone on one side thereof and is in a region of overlap with one side of another zone, and said step of scanning the zone to develop intensity signals includes developing an electrical intensity signal at a second position which is correspondingly placed on the other side of the first said zone and in a region free of overlap, developing a further electrical intensity signal at a third position which is correspondingly placed on the other side of said other zone and in a position free of overlap, and utilzing as the zone intensity signal for said one position a value derived electronically from the intensity signal developed thereat and the ratio of the intensity signals developed at said second and third positions.
Claim 11
Dependent Claim
24 words
Method according to claim 1 wherein the positions represented in said sum signal include a plurality of positions on each of said scan paths.
Claim 12
Dependent Claim
43 words
Method according to claim 1 wherein the positions represented in said sum signal are all on one scan path, said method including deriving sum signals for each said scan path and comparing such individual sum signals with corresponding sets of reference sum signals.
Claim 13
Dependent Claim
173 words
Method according to claim 1 wherein said scan paths include at least one path spaced beyond each end of the zone, and said step of scanning the zone to develop electrical intensity signals is repeated at a series of definite times as the individual zone develops, and said method includes deriving electronically for each of said times, as a measure of the length of the zone, an electronic signal representing the separation of the two outermost scan paths that include at least one said position within the zone for which said intensity signal has a distinct excess over intensity signals at positions outside the zone, extrapolating said zone length signals back in time to zero value to determine a time of initial appearance of the zone, and comparing the resulting time of initial appearance of the zone with a set of reference values derived by similar extrapolation to zero of corresponding zone length signals representing respective known concentrations of said protein, thereby providing a further quantitative measure of the concentration of said protein.
Claim 14
Dependent Claim
62 words
Method according to claim 1 including the steps of deriving electronically from said electrical intensity signals a further quantitative measure of the concentration of said protein, which measure differs characteristically from the first said quantitative measure in presence of certain abnormalities of said protein, and comparing the first said quantitative measure and said further quantitative measure to detect presence of such abnormality.
Claim 15
Dependent Claim
210 words
Method of obtaining a quantitative measure of the concentration of a protein in an antigen sample which has been subjected to immunoelectrophoresis, said method comprising scanning the zone by optical means under dark field illumination at a selected time following initiation of said diffusion to develop a plurality of electrical intensity signals representing the intensity of the scattered light at respective positions which form a two-dimensional array distributed partly within the zone and partly outside the zone, deriving electronically from said intensity signals a plurality of electrical parameter signals representing respective zone parameters, said parameters including at least one parameter exhibiting substantially uniform values for normal and abnormal protein fractions and at least one other parameter exhibiting characteristically different values for normal and abnormal protein fractions, comparing the parameter signal for at least said one parameter with a set of reference parameter signals derived from corresponding measurements of reference zones produced by equivalent immunoelectrophoresis of a plurality of reference antigen solutions containing respective known concentrations of said protein to provide a quantitative measure of the concentration of said protein in said sample, and electronically analyzing the relative values of said parameter signals for a plurality of said parameters including said other parameter to detect presence of an abnormal protein fraction.
Claim 16
Dependent Claim
210 words
Method of obtaining a quantitative measure of the concentration of a protein in an antigen sample which has been subjected to immunoelectrophoresis, said method comprising scanning the zone by optical means under dark field illumination at a selected time following initiation of said diffusion to develop a plurality of electrical intensity signals representing the intensity of the scattered light at respective positions which form a two-dimensional array distributed partly within the zone and partly outside the zone, deriving electronically from said intensity signals a plurality of electrical parameter signals representing respective zone parameters, said parameters including at least one parameter exhibiting substantially uniform values for normal and abnormal protein fractions and at least one other parameter exhibiting characteristically different values for normal and abnormal protein fractions, comparing the parameter signal for at least said one parameter with a set of reference parameter signals derived from corresponding measurements of reference zones produced by equivalent immunoelectrophoresis of a plurality of reference antigen solutions containing respective known concentrations of said protein to provide a quantitative measure of the concentration of said protein in said sample, and electronically analyzing the relative values of said parameter signals for a plurality of said parameters including said other parameter to detect presence of an abnormal protein fraction.
Claim 17
Dependent Claim
33 words
Method according to claim 14 wherein said one parameter comprises a summation of intensity signals for positions distributed substantially uniformly in said zone, and said other parameter comprises the length of said zone.
Claim 18
Dependent Claim
36 words
Method according to claim 14 wherein said one parameter comprises a summation of intensity signals for positions distributed substantially uniformly in said zone, and said other parameter comprises the time of initial appearance of said zone.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1981-06-26 | 1981-12-26 | 1982-06-27 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1985-06-26 | 1985-12-26 | 1986-06-27 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1989-06-26 | 1989-12-26 | 1990-06-27 | $7700.00 | Window Closed / Lapsed |