Texas Health Care PLLCTexas Health Care 923 Pennsylvania Ave STE 100, Fort Worth, TX 76104 8179200484 (phone), 8179200068 (fax)
Languages:
English Spanish
Description:
Ms. Lee works in Fort Worth, TX and specializes in Otolaryngology. Ms. Lee is affiliated with Baylor All Saints Medical Center, Baylor Surgical Hospital Fort Worth, John Peter Smith Health Network and Texas Health Harris Methodist Hospital Fort Worth.
Patrick A. McKee - Oklahoma City OK, US Kyung N. Lee - Oklahoma City OK, US Kenneth W. Jackson - Edmond OK, US Victoria J. Christiansen - Oklahoma City OK, US
Assignee:
The Board of Regents of the University of Oklahoma - Norman OK
International Classification:
A61K 35/14
US Classification:
530380, 530350
Abstract:
Human α-antiplasmin (αAP) is the major inhibitor of the proteolytic enzyme plasmin that digests fibrin. Two forms of αAP circulate in human plasma: a 464-residue protein, which we have termed “pro”-form, or αAP, and an N-terminally-shortened 452-residue “activated”-form, or αAP. The latter becomes crosslinked to fibrin by activated factor XIII about 5-fold more rapidly than αAPand makes fibrin resistant to digestion by plasmin. A new human plasma proteinase has been identified herein that cleaves the Pro12-Asn13 bond of αAPto yield αAP. This enzyme is identified herein as Antiplasmin Cleaving Enzyme (APCE).
Substrates And Inhibitors Of Antiplasmin Cleaving Enzyme And Methods Of Use
The present invention is directed toward inhibitors of antiplasmin cleaving enzyme for use in various therapies related to fibrin and α-antiplasmin, and to substrates of APCE, which may be used, for example, in screening methods for identifying such inhibitors. The present invention is further directed to methods of treating or inhibiting atherosclerosis and thrombus disorders by altering the rations of types of plasma α-antiplasmin.
Methods Of Screening For Inhibitors Of Antiplasmin Cleaving Enzyme
Patrick McKee - Oklahoma City OK, US Kyung Lee - Oklahoma City OK, US Kenneth Jackson - Edmond OK, US Victoria Christiansen - Oklahoma City OK, US
International Classification:
G01N 33/53 C12N 9/68
US Classification:
435007100, 435217000
Abstract:
Human α-antiplasmin (αAP) is the major inhibitor of the proteolytic enzyme plasmin that digests fibrin. Two forms of αAP circulate in human plasma: a 464-residue protein, which we have termed “pro”-form, or αAPand an N-terminally-shortened 452-residue “activated”-form, or αAP. The latter becomes crosslinked to fibrin by activated factor XIII about 5-fold more rapidly than αAPand makes fibrin resistant to digestion by plasmin. A new human plasma proteinase has been identified herein that cleaves the Pro12-Asn13 bond of αAPto yield αAP. This enzyme is identified herein as Antiplasmin Cleaving Enzyme (APCE). Novel inhibitors of circulating APCE can diminish αAP inhibitory capacity within forming fibrin or blood clots thereby making fibrin deposits or blood clots more susceptible to removal by plasmin. Patients who are susceptible to atherosclerotic plaque formation or are susceptible to developing thrombi that compromise organ function will benefit by therapies providing such inhibitors on a long term basis.
Substrates And Inhibitors Of Antiplasmin Cleaving Enzyme And Fibroblast Activation Protein And Methods Of Use
Patrick A. McKee - Oklahoma City OK, US Kenneth W. Jackson - Edmond OK, US Kyung N. Lee - Oklahoma City OK, US Victoria J. Christiansen - Oklahoma City OK, US
The presently disclosed and claimed inventive concepts include inhibitors of antiplasmin cleaving enzyme (APCE) and fibroblast activation protein alpha (FAP) which can be used in various therapies related to disorders of fibrin and α-antiplasmin and abnormal cell proliferation. The presently disclosed and claimed inventive concepts also include substrates of APCE and FAP, which may be used, for example, in screening methods for identifying such inhibitors. The presently disclosed and claimed inventive concepts further include, but are not limited to, methods of treating or inhibiting atherosclerosis and thrombus disorders by altering the ratios of types of plasma α-antiplasmin and to methods of treating conditions involving abnormal cell proliferation such as cancers.
Substrates And Inhibitors Of Antiplasmin Cleaving Enzyme And Fibroblast Activation Protein And Methods Of Use
The presently disclosed inventive concept(s) include inhibitors of antiplasmin cleaving enzyme (APCE) and fibroblast activation protein alpha (FAP) which can be used in various therapies related to disorders of fibrin and α-antiplasmin and abnormal cell proliferation. The presently disclosed inventive concept(s) also include substrates of APCE and FAP, which may be used, for example, in screening methods for identifying such inhibitors. The presently disclosed inventive concept(s) further include, but are not limited to, methods of treating or inhibiting atherosclerosis and thrombus disorders by altering the ratios of types of plasma α-antiplasmin and to methods of treating conditions involving abnormal cell proliferation such as cancers.
Substrates And Inhibitors Of Antiplasmin Cleaving Enzyme And Fibroblast Activation Protein And Methods Of Use
- Norman OK, US Kenneth W. Jackson - Edmond OK, US Kyung N. Lee - Oklahoma City OK, US Victoria J. Christiansen - Oklahoma City OK, US
International Classification:
C07K 5/02
US Classification:
548405
Abstract:
The presently disclosed and claimed inventive concepts include inhibitors of antiplasmin cleaving enzyme (APCE) and fibroblast activation protein alpha (FAP) which can be used in various therapies related to disorders of fibrin and α-antiplasmin and abnormal cell proliferation. The presently disclosed and claimed inventive concepts also include substrates of APCE and FAP, which may be used, for example, in screening methods for identifying such inhibitors. The presently disclosed and claimed inventive concepts further include, but are not limited to, methods of treating or inhibiting atherosclerosis and thrombus disorders by altering the ratios of types of plasma α-antiplasmin and to methods of treating conditions involving abnormal cell proliferation such as cancers.
omprehensive Cancer Center at UT Southwestern Medical Center, as well as Dr. Ratna Vadlamudi, professor of obstetrics and gynecology at UT Health San Antonio. Dr. Tae-Kyung Lee, a former UTD research scientist in Ahn's Bio-Organic/Medicinal Chemistry Lab, was also involved in synthesizing the compound.
Date: Jun 10, 2022
Category: Health
Source: Google
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