Last month, Morphotek, Inc., a subsidiary of Eisai Co., Ltd. based in Exton, Pennsylvania, announced that it had been granted U.S. Patent No. 7,235,643 ("Antibodies and methods for generating genetically altered antibodies with high affinity," issued June 26, 2007). This is the eleventh U.S. Patent awarded to Morphotek, Inc.
Prior to cell division, gene duplication is accomplished by the parent cell's replication of the cell's genetic material. Errors in replication can lead to mutations among the duplicated genes; however, DNA repair mechanisms, such as mismatch repair (MMR), normally repair such mutations prior to cell division. MMR is a proofreading mechanism by which the cell checks the genetic coding between the two copies of the genetic material to ensure that the genes are, in fact, copies of one another. Normally, cell division occurs only upon completion of MMR. In cells where MMR is dysfunctional, mutations accumulate through the genome to the point where sibling cells have traits different from the parents. Morphogenics is a technology whereby the MMR process is selectively regulated within a living host. Through the regulation of morphogenics and targeted mutation, scientists can accelerate cellular evolution, thereby creating unique organisms ideal for the study of disease pathogenesis or other commercial applications.
The '643 patent covers both Morphotek's proprietary human MORPHODOMA® technology, which combines an ex vivo immunization with morphogenics. The resultant antibodies naturally target specific disease-associated antigens.
The '643 patent issued from U.S. Application No. 10/243,130 which was filed on September 13, 2002 and which was a continuation-in-part of U.S. Application No. 09/707,468, filed November 7, 2000, which is now U.S. Patent No. 6,808,894. Independent claim 1 recites:
1. A method for producing a monoclonal antibody having an increased affinity for the antigen to which it binds relative to a monoclonal antibody comprising a heavy chain variable region comprising SEQ ID NO: 18, the method comprising substituting Alanine at the sixth position of SEQ ID NO:18 with Proline, whereby the affinity of the produced monoclonal antibody for said antigen is increased.
Suresh Pillai, Ph.D., is a molecular biologist and a third-year law student at DePaul University College of Law. Dr. Pillai was a member of MBHB's 2007 class of summer associates, and is currently working as a law clerk at MBHB.
I like this blog, but I didn't even get past the headline of this particular entry - I've got an aversion to the expression "so-and-so was awarded a patent", which to me is an expression used by people who don't know much about patent law. You're *awarded* a prize or an honor; you don't apply for an award, someone else nominates you for it; and there usually aren't strict criteria for the awarding of awards. In contrast, you're *granted* patent because you apply for one (including payment of certain fees), and the application and claimed invention meet certain statutory requirements. Anyone who's application and the invention claimed therein meets those requirements is granted a patent.
Posted by: Dan Feigelson | December 16, 2007 at 03:32 AM
Dan:
Thank you for your comment. I have tweaked the title and opening of the post a little, but believe that you are perhaps being a little too harsh with respect to the difference between "grant" and "award." A quick search of www.thefreedictionary.com shows that "awarded" means "to grant as merited or due" or "to give as legally due." Therefore, while you are certainly entitled to your preference for the term "grant," I must disagree with you that the use of the term "award" indicates that the author "[doesn't] know much about patent law." Nevertheless, thanks for your comment and for reading Patent Docs.
Don
Posted by: Donald Zuhn | December 16, 2007 at 12:24 PM