Method for studying enzymatic and other biochemical reactions

Claim 2

Method for determining the activity of concentration in a sample, of a biochemical substance which biochemically affects a substrate that is specific for the biochemical substance which comprises: providing metallic or semiconductor electrodes coated with said substrate, determining as a control value, the capacitance in a measuring device of said metallic electrodes or semiconductor electrodes coated with said substrate, introducing the sample to be tested for the determination of the activity or concentration of said substance into said measuring device so as to contact said coated electrodes with said sample, measuring the change in capacitance due to a change in the amount of biochemically uneffected substrate coated on said electrodes, and thereby obtaining a quantitative measure of the activity or concentration of said substance, present in the sample and affecting the specific substrate on the electrodes.

Claim 3

The method of claim 1 wherein the coated electrodes are prepared by immersing the metallic or semiconductor electrodes in a solution containing a substrate which is capable of adsorbing on the surfaces of said electrodes.

Claim 4

The method of claim 2 wherein the molecules of said substrate adsorbed on the electrode surfaces completely or partially dissociate and thereby are desorbed upon introducing said substance.

Claim 5

The method of claim 2 wherein the molecules of said substrate adsorbed on the electrode surface bind molecules of said substance thereby increasing the layer thickness of the electrode surfaces upon introducing said substance.

Claim 6

The method of claim 1 which comprises measuring the capacitance between the electrodes by using an electric impedance bridge.

Claim 7

The method of claim 1 wherein said substance whose activity or concentration is to be determined are serine proteases, and said substrate is synthetic splittable polypeptide specific for serine proteases.

Claim 8

The method of claim 6 wherein said substrate is represented by the formula: ##STR1## or salts thereof, where R 1 is hydrogen, an alkyl-carbonyl having 1-12 carbon atoms, a ω-aminoalkyl-carbonyl having 1-12 carbon atoms in a straight chain, cyclohexyl-carbonyl, a ω-cyclohexylalkyl-carbonyl having 1-6 carbon atoms in a straight chain, 4-amino ethyl-cyclohexyl-carbonyl, benzoyl, benzoyl substituted with one or more substituents selected from halogen atoms, methyl, amino and phenyl groups, a ω-phenyl-alkylcarbonyl having 1-6 carbon atoms in a straight chain, benzenesulphonyl, 4-toluene-sulphonyl or Nα-benzoyl-phenylalanyl; R 2 is phenyl, benzyl, 4-hydroxy-benzyl, 4-methoxybenzyl or 4-methylbenzyl; R 3 is a straight, branched or cyclic alkyl having 3-8 carbon atoms, phenyl, or benzyl; n is 3 or 4; R 4 is hydrogen or quanyl; and R 5 is phenyl, nitrophenyl, methylnitrophenyl, dinitrophenyl, naphthyl, nitronaphthyl, quinolyl or nitroquinolyl.

Claim 9

The method of claim 4 wherein the molecules of said substrate are inhibitors to the molecules of said substance.

Claim 10

The method of claim 4 wherein the molecules of said substrate are receptors for hormones whose activity or concentration is to be determined.

Claim 11

The method of claim 1 wherein said biochemical substances are enzymes.

Claim 12

The method of claim 1 wherein said electrodes are metallic electrodes.

Claim 13

The method of claim 11 wherein said electrodes are selected from the group consisting of platinum, copper, silver, molybdenum, titanium, gold, palladium, and nickel chrome.

Claim 14

The method of claim 11 wherein said electrodes are platinum electrodes.

Claim 15

The method of claim 11 wherein said electrodes are coated with a monomolecular layer of said substrate.

Claim 16

The method of claim 1 wherein said substrate is chemically bound to said electrode.

Claim 17

The method of claim 1 wherein said surfaces of the electrodes are not entirely saturated with said substrate.