Enzo Biochem Inc. v. Applera Corp.

702 F. App'x 971
CourtCourt of Appeals for the Federal Circuit
DecidedAugust 2, 2017
Docket2016-1881
StatusUnpublished

This text of 702 F. App'x 971 (Enzo Biochem Inc. v. Applera Corp.) 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
Enzo Biochem Inc. v. Applera Corp., 702 F. App'x 971 (Fed. Cir. 2017).

Opinion

O’Malley, Circuit Judge.

Enzo Biochem, Inc., Enzo Life Sciences, Inc., and Yale University (collectively, “Enzo”) appeal from the District of Connecticut’s entry of summary judgment in favor of Applera Corp. and Tropix, Inc. (collectively, “Applera”). See Enzo Biochem, Inc. v. Applera Corp. (District Court Decision), No. 3:04cv929 (JBA), 2016 WL 706164, 2016 U.S. Dist. LEXIS 20904 (D. Conn. Feb. 22, 2016). Because the district court accurately interpreted this court’s decision regarding the proper construction of the claims in U.S. Patent No. 5,449,767 (“the ’767 patent”) and correctly analyzed Enzo’s doctrine of equivalents argument, we affirm.

I. Background

With this appeal, this court now has considered this infringement action on three separate occasions over the course of thirteen years of litigation between these parties. We assume the parties are familiar with the background facts, and we therefore recite only those facts relevant to our decision in this appeal,

A. DNA and RNA Sequencing and the ’767 Patent

As explained in the previous appeals, DNA and RNA are composed of a series of units called “nucleotides.” Enzo Biochem, Inc. v. Applera Corp. (Enzo II), 780 F.3d 1149, 1150 (Fed. Cir. 2015) (quoting Enzo Biochem, Inc. v. Applera Corp. (Enzo I), 599 F.3d 1325, 1328 (Fed. Cir. 2010)). Each nucleotide is composed of a nitrogenous base, a pentose sugar, and a phosphate group. Id. at 1160-51 (quoting Enzo I, 599 F.3d at 1328). Two strands of DNA or RNA having complementary nitrogenous bases will “hybridize” to form a double-stranded complex. Id. at 1151 (quoting Enzo I, 599 F.3d at 1328).

The technology at issue in this case deals with the use of nucleotide probes to detect the presence of a particular DNA or RNA sequence in a sample or to identify an otherwise unknown DNA sequence. In our previous opinions, we explained how hybridization can be used to detect the presence of a nucleic acid:

Because hybridization occurs in a predictable manner between complementary strands, it is possible to detect the presence of a nucleic acid of interest in a sample. For example, a chemical entity, called a “label,” can be attached to or incorporated into a nucleic acid strand of a known sequence, called a “probe,” which will hybridize with a complementary, sequence of interest, called a “target.” Once the probe is hybridized with the target, a detectable signal is generated either from the label itself (referred to as “direct detection”) or from a secondary chemical agent that is bound to the label (referred to as “indirect detection”). If a signal is detected from the sample after all unhybridized probes have been removed, detection of the signal implies the presence of a target in that sample.

Id. (quoting Enzo I, 599 F.3d at 1328).

The ’767 patent explains that “[m]any procedures employed in biomedical research and recombinant DNA technology rely heavily on the use of’ radioactive labels, such as isotopes of hydrogen, phos *973 phorus, carbon, or iodine. ’767 patent, col. 1 11. 23-27. When used as labels, these radioactive compounds provide “useful indicator probes that permit the user to detect, monitor, localize, or isolate nucleic acids and other molecules of scientific or clinical interest, even when present in only extremely small amounts.” Id. at col. 1 11. 27-32. But the ’767 patent notes that the use of these radioactive materials has “serious limitations and drawbacks.” Id. at col. 1 11. 35-37. For example, elaborate safety precautions are necessary for the preparation, utilization, and disposal of the isotopes to avoid potentially hazardous levels of exposure to the radioactive material. Id. at col. 111. 27-41. The radioactive material also is expensive to use and purchase. Id. at col. 111. 41-46. And it is often unstable, .with a short shelf-life. Id. at col. 111. 46-52.

As an alternative to the use of radioactive labels, the ’767 patent explains that “a series of novel nucleotide derivatives that contain biotin, iminobiotin, lipoic acid, and other determinants attached covalently to the pyrimidine or purine ring have been synthesized.” Id. at col. 2 11. 63-68. These nucleotide derivatives interact “specifically and uniquely with proteins such as avidin or antibodies.” Id. at col. 3 11. 2-3. “If avidin is coupled to potentially demonstrable indicator molecules, including fluorescent dyes, ... electron-dense reagents, ... or enzymes capable of depositing insoluble reaction products, ... the presence, location, or quantity of a biotin probe can be established.” Id. at col. 1 11. 61-67.

The ’767 patent asserts that the use of this modified detection approach provides “detection capacities equal to or greater than procedures which utilize radioisotopes and [it] often can be performed more rapidly and with greater resolving power,” Id. at col. 3 11. 9-13.- The ’767 patent further describes these new nucleotide derivatives as providing an approach to detection that is “relatively inexpensive[ ],” does not require “elaborate safety procedures,” uses “chemically stable” derivatives, and allows for “the development of safer, more economical, more rapid, and more reproducible research and diagnostic procedures.” Id. at col. 3 11.14-28.

Claim 1 of the ’767 patent covers an oligo- or polynucleotide containing a nucleotide having the following structure:

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See id. at col. 30 1. 48-eol. 31 1. 21. The disputed language of claim 1 involves the following limitation: “wherein A comprises at least three carbon atoms and represents at least one component of a signaling moiety capable of producing a detectable signal....” Id. at col. 3011. 66-68.

All other asserted claims of the ’767 patent depend, directly or indirectly, from claim 1. Claim 8 depends from claim 1 and claims, “[a]n oligo- or polynucleotide of claim 1 wherein the linkage group includes the moiety -CH2-NH-.” Id. at' col. 31 11. 36-37. Claim 67 depends from claim 1 and claims, “[a]n oligo- or polynucleotide of claim 1 or 48 wherein A comprises an indicator molecule.” Id. at col. 36 11. 42-43. Claim 68 depends from claim 67 and claims, “[a]n oligo- or polynucleotide of claim 67 wherein said indicator molecule is fluorescent, electron dense, or is an enzyme capable of depositing insoluble reac *974 tion products.” Id. at col. 36 11. 44-47. Claim 70 depends from claim 68 and claims, “[a]n oligo- or polynucleotide of claim 68 wherein the fluorescent indicator molecule is selected from the group consisting of fluorescein and rhodamine.” Id. at col. 3611. 51-63.

B. Procedural History

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