Illumina Cambridge Ltd. v. Intelligent Bio-Systems, Inc.

638 F. App'x 999
CourtCourt of Appeals for the Federal Circuit
DecidedJanuary 29, 2016
Docket2015-1123, 2015-1243
StatusUnpublished

This text of 638 F. App'x 999 (Illumina Cambridge Ltd. v. Intelligent Bio-Systems, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Illumina Cambridge Ltd. v. Intelligent Bio-Systems, Inc., 638 F. App'x 999 (Fed. Cir. 2016).

Opinion

LOURIE, Circuit Judge.

Illumina Cambridge Ltd. (“Illumina”) appeals from the final written decisions of the united States Patent and Trademark Office, Patent Trial and Appeal Board (“the Board”) cancelling all challenged claims of its U.S. Patents 7,057,026 (“the '026 patent”) and 8,158,346 (“the '346 patent”) and denying entry of substitute claims in two inter partes review proceedings. Intelligent Bio-Systems, Inc. v. Illumina Cambridge Ltd., IPR2013-00128, Paper No. 92, 2014 WL 3736339 (P.T.AB. July 25, 2014); Intelligent Bio-Systems, Inc. v. Illumina Cambridge Ltd., IPR2013-00266, Paper No. 73, 2014 WL 5490579 (P.T.A.B. Oct. 28, 2014). Because the Board did not err in determining that illumina failed to show that the proposed substitute claims are patentable over the prior art of record, and thus did not err in denying in part the motions to amend, we affirm.

Background

Illumina owns the '026 and '346 patents, which are both directed to DNA sequencing by synthesis (“SBS”) with non-natural nucleotides. As the name implies, SBS allows one to determine the composition of a target DNA sequence by synthesizing new copies of the DNA. Briefly, the synthesis process involves splitting the double helix of a target DNA molecule into two strands and then' incorporating complementary labeled nucleotides onto each strand to create two double helices. Non-natural nucleotides contain a non-natural base, i.e., a modified purine or pyrimidine base.

The '026 patent is directed to nucleotide compositions of matter, while the '346 patent relates to methods of using such nucleotides. As the issues relating to the patentability of the claims of both of these patents are essentially the same, we evaluate both of them here in one opinion and decision.

An exemplary non-natural nucleotide of the two patents, pictured below, has a deoxyribose ring, with a protecting group attached at the 3'-OH position and a label connected to the non-natural base (here, deazapurine) by a linker (here, containing *1001 a disulfide linkage). According to the '026 and '346 patents, the linker and the protecting group for the claimed non-natural nucleotides are cleavable under identical conditions. .

[[Image here]]

The claimed SBS methods involve incorporating the non-natural nucleotides into multiple copies of a target DNA molecule, one at a time for each strand in a stepwise fashion. At each step, the signal from the label is detected, indicating which nucleotide has been incorporated. Because a second nucleotide is added to the newly forming strand by its phosphate group binding to the 3'-OH position of a first nucleotide, a protecting group already attached at that position blocks the bond from being formed, and thus prevents multiple nucleotides from being added to the strand in the same step. Once the incorporated nucleotide is identified by the signal from its label, its attached protecting group is cleaved (or “deblocked”), allowing the next nucleotide to be incorporated. Ideally, the label is also cleaved at this time, clearing the slate for the next nucleotide’s signal. This stepwise process repeats until the sequence of the target DNA molecule has been determined.

If a protecting group is not properly cleaved, then the newly forming strand will not incorporate the next complementary nucleotide in that step and will become “out of phase” with the other strands, ie., its sequence will no longer match the others in any future steps. In contrast, if a linker for a label fails to be cleaved, the strand will still be in phase despite its incorrect or mixed signals; moreover, the linker will likely be cleaved, and the signal corrected, in subsequent cycles.

In 2012, a third party filed suit against Illumina, asserting several DNA sequencing patents for which Intelligent Bio-Systems, Inc. (“Intelligent Bio-Systems”) is the exclusive licensee. In its answer, Illu-mina counterclaimed that Intelligent Bio-Systems infringed Illumina’s '026 and '346 patents. Intelligent Bio-Systems then filed petitions for inter partes review at the Board, challenging claims 1-8 of the '026 patent and claims 1, 2, 4, 11, 12, 17, 18, and 19 of the '346 patent. The district court case was stayed pending resolution of these and several other related inter partes review proceedings.

The Board instituted review of both the '026 and '346 patents on the grounds of *1002 anticipation and obviousness. 2015-1123 Joint App. (“1123-J.A.”) 332-350; 2015-1243 Joint App. (“1243-J.A.”) 208-221. Instead of submitting responses to the institution decisions, Illumina filed motions to amend, requesting cancellation of all challenged claims of both patents, and entry of substitute claims 9-12 for the '026 patent (“'026-substitute claims”), 1123-J.A. 501-503, and claims 20-26 for the '346 patent (“'346-substitute claims”), 1243-J.A. 278-279. Noting that the cancellation requests were not contingent on the original claims being found unpatentable, the Board granted Illumina’s motions in part, cancelling all of the challenged claims of both patents. 1123-J.A. 29-30; 1243-J.A. 23.

The Board then examined the proposed substitute claims for the '026 patent. Representative proposed substitute claim 9 for the '026 patent reads as follows, with Illumina’s annotations for replacing claim 1:

9. A nucleotide triphosphate or-nudeo-side molecule, having a 7-deazapurine base that is linked to a detectable label via a cleavable linker, wherein the cleavable linker is attached to the 7-position of the 7-deazapurine base and wherein the cleavable linker contains a disulfide linkage, and wherein the núcleo tide triphosphate molecule has a ribose or deoxyribose sugar moiety comprising a protecting group attached via the 2' or 3' oxygen atom, and the disulfide linkage of the cleavable linker and the protecting group are cleavable under identical conditions.

1123-J.A. 30. The Board found only one new limitation that is different from the original claims: that the cleavable linker “contains a disulfide linkage.” 1123-J.A. 30.

Starting with the premise that the obviousness of using a disulfide linkage was the main issue to be decided, the Board found that all of the claim limitations were described in the prior art. 1123-J.A 37-39. The Board also found that the prior art provided a reason to use a disulfide linkage to attach a label to a base of a nucleotide, including for DNA sequencing, and with a reasonable expectation of success. 1123-J.A. 40-42. Because the proposed substitute claims do not require a disulfide linkage between the protecting group and the 3'-OH, the Board rejected Illumina’s argument that the1 prior art’s requirement of greater than 90% cleavage efficiency for a protecting group also applied to the ■ claimed disulfide linkage. 1123-J.A. 42-44. Even so, the Board also found that one of skill in the art would have expected to achieve more than 90% cleavage efficiency of the disulfide bond by routine experimentation. 1123-J.A. 44-50. The Board determined that Illumina had not met its burden of showing that one of skill in the art would not have had a reasonable expectation of success,

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Bluebook (online)
638 F. App'x 999, Counsel Stack Legal Research, https://law.counselstack.com/opinion/illumina-cambridge-ltd-v-intelligent-bio-systems-inc-cafc-2016.