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- Rachel Bar-Shavit
- Jewish Hospital and Departments of Pathology and Medicine and Division of Cell Biology, Washington University, St. Louis, Missouri 63130
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- Arnold Kahn
- Jewish Hospital and Departments of Pathology and Medicine and Division of Cell Biology, Washington University, St. Louis, Missouri 63130
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- George D. Wilner
- Jewish Hospital and Departments of Pathology and Medicine and Division of Cell Biology, Washington University, St. Louis, Missouri 63130
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- John W. Fenton
- Center for Laboratories and Research, New York State Department of Health, Albany 12201
抄録
<jats:p>Human α-thrombin is a potent chemoattractant for human monocytes, with optimum activity occurring at about 10 nanomoles per liter. A variety of thrombins that were chemically modified to alter procoagulant or esterolytic functions showed a similar optimum activity, but complexes of prothrombin or α-thrombin with either antithrombin III or hirudin did not. These findings indicate that the regions in thrombin responsible for monocyte chemotaxis are proximate to those involved in certain protein recognition interactions of α-thrombin (for example, hirudin binding) but are distinct from the catalytic site and from certain exosites required for clotting.</jats:p>
収録刊行物
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- Science
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Science 220 (4598), 728-731, 1983-05-13
American Association for the Advancement of Science (AAAS)
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キーワード
詳細情報 詳細情報について
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- CRID
- 1362262944664193664
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- NII論文ID
- 30020523044
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- ISSN
- 10959203
- 00368075
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- データソース種別
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