合作案例

December 27, 2023
Dr. Tim Shi
Hefei Sciben Biotech Co. Ltd, Jiulong Rd,
Jingkai District, Hefei,
Anhui Province, PR China
Dear Dr. Shi,
As you know during the time you spent in my laboratory as a post-doctoral research fellow, we work on the role
of the protein tyrosine phosphatases in cell signaling and disease. Specifically, we have been focusing on a sub
family of protein tyrosine phosphatases known as dual-specificity phosphatases that are involved in the
dephosphorylation of the MAP kinases. These MAP kinase phosphatases (MKPs) have been shown by you and
others to be important for the progression of many important human diseases such as dystrophic muscle disease,
obesity and metabolism as well as inflammatory processes such as fibrosis. With our recent discovery that the
MKPs are druggable there is increasing interest in the potential for the MKPs to be used as therapeutics against
certain human diseases.
As my laboratory continues to work on the MKPs we have required the use of, and have become very reliant on,
the antibodies to the MKPs for our studies. Unfortunately, the quality of the antibodies to the MKPs continues to
be extremely poor. This is not a recent challenge but has plagued the MKP field for the last three decades and has
significantly impeded research progress. Given our recent discussions of your companies advanced capabilities in
producing antibodies that are rigorously validated we would be very enthusiastic for you to generate monoclonal
antibodies to the MKP family of enzymes. These will include the following MKPs; MKP1/DUSP1,
MKP2/DUSP4, MKP3/DUSP6, MKP5/DUSP10 and MKP7/DUSP16. I understand that this is an extensive list
however, if you are successful in developing high quality monoclonal antibodies to these MKPs this would
provide a significant boost to not only our research but the field in general.
In order to facilitate the successful development of these MKP monoclonal antibodies my laboratory will be
willing to participate by providing quality control and validation experiments to support this work. If successful,
we will use these antibodies in our research studies and publish the results using these antibodies. I will also be
willing through my national and international speaking engagements to further publicize the results of these MKP
antibodies in unpublished work to the research community. To let you know, I am scheduled to deliver several
national and international meetings in 2024. In this way, the scientific community will be able to see the quality of
these reagents and will thus provide you with the best form of advertisement to promote your company. I request
that before you endorse the use of any of these antibodies that you obtain my permission prior and that we are in
mutual agreement as to the use of any data that my lab may provide to you as part of our collaboration.
I wish you the best of success and I look forward to a productive collaboration with you and the company on this
project. Please do not hesitate to contact me for further information or questions.
Yours Sincerely,
 
 
Anton M. Bennett, Ph.D.
Dorys McConnell Duberg Professor and Vice-Chair of Pharmacology
Director, Yale Center for Molecular and Systems Metabolism
Director, Minority Affairs BBS Graduate Program

Yale University

Anton M. Bennett, Ph.D.
Dorys McConnell DubergProfessor
of Pharmacology
Department of Pharmacology
Yale University School of Medicine
P.O. Box 208066
New Haven
Connecticut 06520-8066
Campus address:
Sterling Hall of Medicine
B226D
333 Cedar Street
Telephone: (203) 737-2441
Fax: (203) 737-2738
Email: anton.bennett@yale.edu

Metabolism drives all biological processes, dysregulation of which fuels a plethora of human diseases including diabetes, obesity, cancer, aging, cardiovascular and neurodegenerative diseases. The long-range goal of our research is to unravel temporal and spatial regulation of metabolic pathways in response to environmental and genetic cues, and to design strategies to battle metabolic diseases. Diet and the light/dark cycle are principle environmental cues that control intermediary metabolism. Nutrient flux into the cell triggers the posttranslational modification of intracellular proteins by the amino sugar called N-acetylglucosamine (O-GlcNAc). Our first goal is to elucidate how O-GlcNAc acts as a molecular switch that couples nutrient cues to cellular regulation of signal transduction, transcription and protein degradation. Both light and diet affect the body’s circadian rhythms. Our second goal is to depict molecular pathways that couple the circadian clock to metabolic physiology. We are employing a combination of experimental approaches, including biochemistry, molecular and cellular biology, mouse genetics, genomics, proteomics and metabolomics, to accomplish our research goals.
 

研究领域