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Open AccessJournal ArticleDOI

The Activation of Type 1 and Type 2 Plasminogen by Type I and Type II Tissue Plasminogen Activator

TLDR
In an indirect amidolytic assay involving native human Gluplasminogen and fibrin, type II tPA showed a 2-fold higher activity than type I tPA.
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This article is published in Journal of Biological Chemistry.The article was published on 1995-02-17 and is currently open access. It has received 47 citations till now. The article focuses on the topics: Plasminogen activator inhibitor-1 & Tissue plasminogen activator.

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Citations
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Journal ArticleDOI

Concepts and Principles of O-Linked Glycosylation

TL;DR: The biosynthesis, structures, and functions of O-glycosylation, as a complex posttranslational event, is reviewed and compared and the recent development of novel technologies for glycan analysis promises to yield new insights in the factors that determine site occupancy, structure-function relationship, and the contribution of O -linked sugars to physiological and pathological processes.
Journal ArticleDOI

Gelatinase B functions as regulator and effector in leukocyte biology

TL;DR: Gelatinase B ablation in the mouse leads to altered bone remodeling and subfertility, results in resistance to several induced inflammatory or autoimmune pathologies, and indicates that the enzyme plays a crucial role in development and angiogenesis.
Journal ArticleDOI

Glycosylation: heterogeneity and the 3D structure of proteins.

TL;DR: Glycoproteins generally exist as populations of glycosylated variants (glycoforms) of a single polypeptide and the recognition of identical motifs in different glycans allows a heterogeneous population of glycoforms to participate in specific biological interactions.
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Plasminogen activators and matrix metalloproteases, mediators of extracellular proteolysis in inflammatory demyelination of the central nervous system

TL;DR: Novel treatments for demyelinating diseases may be predicted by specific inhibition of these enzymes, as MMPs modify matrix components, promoting extravasation of lymphocytes and monocytes/macrophages and have the potential to generate encephalitogenic peptides from myelin basic protein.
Journal ArticleDOI

The X-ray crystal structure of full-length human plasminogen

TL;DR: The structure of closed plasminogen reveals that the PAp and SP domains, together with chloride ions, maintain the closed conformation through interactions with the kringle array, and analysis of the structure suggests that KR5 peeling away from thePAp domain may initiate plAsminogen conformational change.
References
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Book ChapterDOI

Plasminogen activators, tissue degradation, and cancer.

TL;DR: This chapter describes two types of plasminogen activators—namely, the urokinase-type plasMinogen activator (u-PA) and the tissue- type plasmineg activator(t-PA), which are essentially different gene products.
Journal ArticleDOI

Purification and characterization of the plasminogen activator secreted by human melanoma cells in culture.

TL;DR: In immunodiffusion, as well as in quenching experiments of the fibrinolytic activities, the melanoma plasminogen activator appeared to be immunologically identical with the uterine tissue plasmineg activator, but unrelated to urokinase.
Journal ArticleDOI

Basic and clinical aspects of fibrinolysis and thrombolysis.

TL;DR: Reduction of infarct size, preservation of ventricular function, and reduction in mortality has been obtained with SK, rt-PA, and APSAC, and thrombolytic therapy has become standard treatment for early acute myocardial infarction.
Journal ArticleDOI

A simple, sensitive spectrophotometric assay for extrinsic (tissue-type) plasminogen activator applicable to measurements in plasma.

TL;DR: An indirect spectrophotometric assay for extrinsic plasminogen activator has been devised, which is based on the parabolic assay of Drapier et al. (5), and the application for intrinsic plasmineogen activation measurements in plasma euglobulin fractions is demonstrated.
Journal ArticleDOI

Measurement of the binding of antifibrinolytic amino acids to various plasminogens

TL;DR: This method requires very small amounts of protein and allows determination of low as well as very high dissociation constants with equal reliability.
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