Claims for Patent: 6,309,823

Summary for Patent: 6,309,823

Title:	Arrays of nucleic acid probes for analyzing biotransformation genes and methods of using the same
Abstract:	The invention provides arrays of immobilized probes, and methods employing the arrays, for detecting mutations in the biotransformation genes, such as cytochromes P450. For example, one such array comprises four probe sets. A first probe set comprises a plurality of probes, each probe comprising a segment of at least three nucleotides exactly complementary to a subsequence of a reference sequence from a biotransformation gene, the segment including at least one interrogation position complementary to a corresponding nucleotide in the reference sequence. Second, third and fourth probe sets each comprise a corresponding probe for each probe in the first probe set. The probes in the second, third and fourth probe sets are identical to a sequence comprising the corresponding probe from the first probe set or a subsequece of at least three nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the four corresponding probes from the four probe sets.
Inventor(s):	Cronin; Maureen T. (Los Altos, CA), Miyada; Charles G (San Jose, CA), Hubbell; Earl A. (Los Angeles, CA), Chee; Mark (Palo Alto, CA), Fodor; Stephen P. A. (Palo Alto, CA), Huang; Xiaohua C. (Mountain View, CA), Lipshutz; Robert J. (Palo Alto, CA), Lobban; Peter E. (Mountain View, CA), Morris; MacDonald S. (Felton, CA), Sheldon; Edward L. (San Diego, CA)
Assignee:	Affymetrix, Inc. (Santa Clara, CA)
Application Number:	08/778,794
Patent Claims:	1. An array of nucleic acid probes immobilized on a solid support, the array comprising at least two sets of probes, (1) a first probe set comprising a plurality of probes, each probe comprising a segment of at least six nucleotides exactly complementary to a subsequence of a reference sequence, the segment including at least one interrogation position complementary to a corresponding nucleotide in the reference sequence, (2) a second probe set comprising a corresponding probe for each probe in the first probe set, the corresponding probe in the second probe set being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least six nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the two corresponding probes from the first and second probe sets; wherein the probes in the first probe set have at least three interrogation positions respectively corresponding to each of three contiguous nucleotides in the reference sequence; provided that the array does not consist of a complete set of probes of a given length, wherein a complete set is all permutations of nucleotides A, C, G and T/U; wherein the reference sequence is from a biotransformation gene. 2. An array of oligonucleotide probes immobilized on a solid support, the array comprising at least four sets of nucleic acid probes, (1) a first probe set comprising a plurality of probes, each probe comprising a segment of at least six nucleotides exactly complementary to a subsequence of a reference sequence, the segment including at least one interrogation position complementary to a corresponding nucleotide in the reference sequence, (2) second, third and fourth probe sets, each comprising a corresponding probe for each probe in the first probe set, the probes in the second, third and fourth probe sets being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least six nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the four corresponding probes from the four probe sets; provided the array does not consist of a complete set of probes of a given length wherein a complete set is all permutations of nucleotides A, C, G and T/U; wherein the reference sequence is from a biotransformation gene. 3. The array of claim 1 wherein the reference sequence is from a gene encoding an enzyme selected from the group consisting of a cytochrome P450, N-acetyl transferase II, glucose 6-phosphate dehydrogenase, pseudocholinesterase, catechol-O-methyl transferase, and dihydropyridine dehydrogenase. 4. The array of claim 2, wherein the reference sequence is from a gene encoding an enzyme selected from the group consisting of a cytochrome P450, N-acetyl transferase II, glucose 6-phosphate dehydrogenase, pseudocholinesterase, catechol-O-methyl transferase, and dihydropyridine dehydrogenase. 5. The array of claim 4, wherein the enzyme is P450 2D6 or P450 2C19. 6. The array of claim 2, wherein the reference sequence includes a site of a mutation and a site of a silent polymorphism. 7. The array of claim 6, wherein the silent polymorphism is in an intron or flanking region of a gene. 8. The array of claim 2, wherein the first probe set has at least 3 interrogation positions respectively corresponding to each of 3 contiguous nucleotides in the reference sequence. 9. The array of claim 2, wherein the array has between 100 and 100,000 probes. 10. The array of claim 2, wherein the probes are linked to the support via a spacer. 11. The array of claim 2, wherein the segment in each probe of the first probe set that is exactly complementary to the subsequence of the reference sequence is 9-21 nucleotides. 12. An array of nucleic acid probes immobilized on a solid support, the array comprising at least one pair of first and second probe groups, each group comprising a first and second sets of oligonucleotide probes as defined by claim 1; wherein each probe in the first probe set from the first group is exactly complementary to a subsequence of a first reference sequence and each probe in the first probe set from the second group is exactly complementary to a subsequence from a second reference sequence. 13. The array of claim 12, wherein each group further comprises third and fourth probe sets, each comprising a corresponding probe for each probe in the first probe set, the probes in the second, third and fourth probe sets being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least six nucleotides thereof that includes the interrogation position, except that the interrogation position is occupied by a different nucleotide in each of the four corresponding probes from the four probe sets. 14. The array of claim 12, wherein the first reference sequence includes the site of a mutation in the biotransformation gene, and the second reference sequence includes a site of a silent polymorphism within the biotransformation gene or flanking the biotransformation gene. 15. The array of claim 14, wherein the reference sequence is from a gene encoding an enzyme selected from the group consisting of a cytochrome P450, N-acetyl transferase II, glucose 6-phosphate dehydrogenase, pseudocholinesterase, catechol-O-methyl transferase, and dihydropyridine dehydrogenase. 16. The array of claim 14 that comprises at least forty pairs of first and second probe groups, wherein the probes in the first probe sets from the first groups of the forty pairs are exactly complementary to subsequences from forty respective first reference sequences. 17. A block of nucleic acid probes immobilized on a solid support, comprising: a perfectly matched probe comprising a segment of at least six nucleotides exactly complementary to a subsequence of a reference sequence, the segment having a plurality of interrogation positions respectively corresponding to a plurality of nucleotides in the reference sequence, for each interrogation position, three mismatched probes, each identical to a sequence comprising the perfectly matched probe or a subsequence of at least six nucleotides thereof including the plurality of interrogation positions, except in the interrogation position, which is occupied by a different nucleotide in each of the three mismatched probes and the perfectly matched probe; provided the array does not consist of a complete set of probes of a given length, wherein a complete set is all permutations of nucleotides A, C, G and T/U; wherein the reference sequence is from a biotransformation gene. 18. The array of claim 16, wherein the segment of the perfectly matched probe comprises 3-20 interrogation positions corresponding to 3-20 respective nucleotides in the reference sequence. 19. An array of probes immobilized to a solid support comprising at least two blocks of probes, each block as defined by claim 16, a first block comprising a perfectly matched probe comprising a segment exactly complementary to a subsequence of a first reference sequence and a second block comprising a perfectly matched probe comprising a segment exactly complementary to a subsequence of a second reference sequence. 20. The array of claim 19, wherein the first reference sequence is from a wildtype 2D6 gene and the second reference sequence is from a mutant 2D6 gene. 21. The array of claim 19, comprising at least 10-100 blocks of probes, each comprising a perfectly matched probe comprising a segment exactly complementary to a subsequence of at least 10-100 respective reference sequences. 22. An array of nucleic acid probes immobilized on a solid support, the array comprising at least four probes: a first probe comprising first and second segments, each of at least three nucleotides and exactly complementary to first and second subsequences of a reference sequence, the segments including at least one interrogation position corresponding to a nucleotide in the reference sequence, wherein either (1) the first and second subsequences are noncontiguous, or (2) the first and second subsequences are contiguous and the first and second segments are inverted relative to the complement of the firsthand second subsequences in the reference sequence; second, third and fourth probes, identical to a sequence comprising the first probe or a subsequence thereof comprising at least three nucleotides from each of the first and second segments, except in the at least one interrogation position, which differs in each of the probes; provided the array does not consist of a complete set of probes of a given length, wherein a complete set is all permutations of nucleotides A, C, G and T/U; wherein the reference sequence is from a biotransformation gene. 23. A method of comparing a target nucleic acid with a reference sequence comprising a predetermined sequence of nucleotides, the method comprising: (a) hybridizing a sample comprising the target nucleic acid to an array of nucleic acid probes immobilized on a solid support, the array comprising: (1) a first probe set comprising a plurality of probes, each probe comprising a segment of at least six nucleotides exactly complementary to a subsequence of the reference sequence, the segment including at least one interrogation position complementary to a corresponding nucleotide in the reference sequence, wherein the reference sequence is from a biotransformation gene; (2) a second probe set comprising a corresponding probe for each probe in the first probe set, the corresponding probe in the second probe set being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least six nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the two corresponding probes from the first and second probe sets; wherein, the probes in the first probe set have at least three interrogation positions respectively corresponding to each of at least three nucleotides in the reference sequence, and (b) comparing the relative specific hybridization of two corresponding probes from the first and second probe sets; (c) assigning a nucleotide in the target sequence as the complement of the interrogation position of the probe having the greater specific binding; (d) repeating (b) and (c) by comparing the relative specific hybridization of a further two corresponding probes from the first and second probe sets until each nucleotide of interest in the target sequence has been assigned. 24. The method of claim 23, wherein the determining step comprises: (1) comparing the relative specific hybridization of two corresponding probes from the first and second probe sets; (2) assigning a nucleotide in the target sequence as the complement of the interrogation position of the probe having the greater specific hybridization; and (3) repeating (1) and (2) until each nucleotide of interest in the target sequence has been assigned. 25. The method of claim 23, wherein the array further comprises third and fourth probe sets, each comprising a corresponding probe for each probe in the first probe set, the probes in the second, third and fourth probe sets being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least six nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the four corresponding probes from the four probe sets; and the comparing step comprises comparing the relative specific hybridization of four corresponding probes from the first, second, third and fourth probe groups. 26. The method of claim 25, wherein: the reference sequence includes a site of a mutation in the biotransformation gene and a silent polymorphism in or flanking the biotransformation gene; the target nucleic acid comprises one or more different alleles of the biotransformation gene; and the relative specific hybridization of probes having an interrogation position aligned with the silent polymorphism indicates the number of different alleles and the relative specific hybridization of probes having an interrogation position aligned with the mutation indicates whether the mutation is present in at least one of the alleles. 27. The method of claim 25, wherein the determining comprises: (1) comparing the relative specific hybridization of four corresponding probes from the first, second, third and fourth probe sets; (2) assigning a nucleotide in the target sequence as the complement of the interrogation position of the probe having the greatest specific hybridization; (3) repeating (1) and (2) until each nucleotide of interest in the target sequence has been assigned. 28. A method of comparing a target nucleic acid with a reference sequence comprising a predetermined sequence of nucleotides, the method comprising: (a) hybridizing the target nucleic acid to an array of oligonucleotide probes immobilized on a solid support, the array comprising: a perfectly matched probe comprising a segment of at least six nucleotides exactly complementary to a subsequence of a reference sequence, the segment having a plurality of interrogation positions respectively corresponding to a plurality of nucleotides in the reference sequence, wherein the reference sequence is from a biotransformation gene; for each interrogation position, three mismatched probes, each identical to a sequence comprising the perfectly matched probe or a subsequence of at least six nucleotides thereof including the plurality of interrogation positions, except in the interrogation position, which is occupied by a different nucleotide in each of the three mismatched probes and the perfectly matched probe; (b) for each interrogation position, (1) comparing the relative specific hybridization of the three mismatched probes and the perfectly matched probe; (2) assigning a nucleotide in the target sequence as the complement of the interrogation position of the probe having the greatest specific hybridization. 29. The method of claim 28, wherein the target sequence has an undetermined substitution relative to the reference sequence, and the method assigns a nucleotide to the substitution. 30. A method of screening a patient for capacity to metabolize a drug, the method comprising: (a) hybridizing a tissue sample from the patient containing a target nucleic acid to an array of oligonucleotide probes immobilized on a solid support, the array comprising: (1) a first probe set comprising a plurality of probes, each probe comprising a segment of at least three nucleotides exactly complementary to a subsequence of the reference sequence from a biotransformation gene which metabolizes the drug, the segment including at least one interrogation position complementary to a corresponding nucleotide in the reference sequence, (2) a second probe set comprising a corresponding probe for each probe in the first probe set, the corresponding probe in the second probe set being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least three nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the two corresponding probes from the first and second probe sets; wherein, the probes in the first probe set have at least three interrogation positions respectively corresponding to each of at least three nucleotides in the reference sequence, and (b) determining which probes, relative to one another, in the first and second probe sets specifically hybridize to the target nucleic acid, the relative specific hybridization of corresponding probes in the first and second probe sets indicating whether the target sequence contains a mutation relative to the reference sequence, which, if present, impairs the capacity of the patient to metabolize the drug. 31. A method of conducting a clinical trial on a drug, the method comprising: (a) obtaining a tissue sample containing a target nucleic acid from each of a pool of patients; (b) for each tissue sample, hybridizing the target nucleic acid to an array of oligonucleotide probes immobilized on a solid support, the array comprising: (1) a first probe set comprising a plurality of probes, each probe comprising a segment of at least three nucleotides exactly complementary to a subsequence of the reference sequence from a biotransformation gene, the segment including at least one interrogation position complementary to a corresponding nucleotide in the reference sequence, (2) a second probe set comprising a corresponding probe for each probe in the first probe set, the corresponding probe in the second probe set being identical to a sequence comprising the corresponding probe from the first probe set or a subsequence of at least three nucleotides thereof that includes the at least one interrogation position, except that the at least one interrogation position is occupied by a different nucleotide in each of the two corresponding probes from the first and second probe sets; wherein, the probes in the first probe set have at least three interrogation positions respectively corresponding to each of at least three nucleotides in the reference sequence; (c) determining which probes, relative to one another, in the first and second probe sets specifically hybridize to the target nucleic acid, the relative specific hybridization of corresponding probes in the first and second probe sets indicating whether the target sequence contains a mutation relative to the reference sequence selecting a subpool of patients having a target sequence free of the mutation; and (d) administering the drug to the subpool of patients to determine efficacy. 32. The method of claim 31, further comprising combining the drug with a pharmaceutical carrier to form a pharmaceutical composition.

Details for Patent 6,309,823

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132	06/04/1986		2013-10-26
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132			2013-10-26
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	Injection	103132			2013-10-26