Clinical Chemistry
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Clinical Chemistry 46: 38-46, 2000;
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(Clinical Chemistry. 2000;46:38-46.)
© 2000 American Association for Clinical Chemistry, Inc.


Articles

Measurement of Different Forms of Tissue Plasminogen Activator in Plasma

Wayne L. Chandlera, Marcy L. Jascur and Paul J. Henderson

1 Department of Laboratory Medicine, University of Washington, Seattle, WA 98195.
a Address correspondence to this author at: Department of Laboratory Medicine, Box 357110, University of Washington, Seattle, WA 98195. Fax 206-598-6189; e-mail wlc{at}u.washington.edu

Background: We evaluated assays to measure both total tissue plasminogen activator (tPA) and the three principle forms of tPA in plasma: active tPA, tPA complexed with plasminogen activator inhibitor type 1 (PAI-1), and tPA complexed with C1-inhibitor.

Methods: Active tPA was measured by use of an indirect amidolytic assay and immunofunctional assays. tPA/PAI-1, tPA/C1-inhibitor, and total tPA antigen were measured by use of microtiter plates coated with anti-tPA antibodies and, respectively, anti-PAI-1, anti-C1-inhibitor, and anti-tPA antibodies conjugated to peroxidase.

Results: The immunofunctional tPA assay detected 1 U/L (0.001 U/mL) tPA and recovered 108% ± 12% of active tPA added to samples containing high (mean, 60 000 IU/L) PAI-1 activities vs a detection limit of 10 U/L (0.01 U/mL) and 13% ± 25% recovery for the indirect amidolytic tPA activity assay. For measurement of tPA/PAI-1 complex, polyclonal anti-PAI-1 conjugates recovered 112% ± 20% of the expected tPA/PAI-1 vs recovery of only 38% ± 16% when monoclonal anti-PAI-1 conjugates were used. Of three methods tested, two total tPA antigen assays correlated well (r2 = 0.85) and showed recoveries near 100%, whereas the third method showed lower correlations, higher intercepts, and falsely high recovery. A single anti-tPA capture antibody that performed the best in the individual assay evaluations was used to measure the different forms of tPA in 22 samples with a range of tPA and PAI-1 values. The sum of the molar concentrations of active tPA, tPA/PAI-1, and tPA/C1-inhibitor using the optimized methods was equal to 94% ± 7% of measured total tPA.

Conclusion: Optimized assays based on a single anti-tPA capture antibody can be used to accurately measure the major forms of tPA in plasma.




The following articles in journals at HighWire Press have cited this article:


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Anesth. Analg.Home page
M. J. Eisses, K. Seidel, G. S. Aldea, and W. L. Chandler
Reducing Hemostatic Activation During Cardiopulmonary Bypass: A Combined Approach
Anesth. Analg., May 1, 2004; 98(5): 1208 - 1216.
[Abstract] [Full Text] [PDF]


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NEJMHome page
W. L. Chandler, S. Jelacic, D. R. Boster, M. A. Ciol, G. D. Williams, S. L. Watkins, T. Igarashi, and P. I. Tarr
Prothrombotic Coagulation Abnormalities Preceding the Hemolytic-Uremic Syndrome
N. Engl. J. Med., January 3, 2002; 346(1): 23 - 32.
[Abstract] [Full Text] [PDF]




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