Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation

When blood is exposed to variety of artificial surfaces and biologic substances, the plasma proteins factor XII (FXII) and prekallikrein undergo reciprocal proteolytic conversion to the proteases αFXIIa and α-kallikrein by a process called contact activation. These enzymes contribute to host-defense...

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Main Authors: Ivanov, Ivan, Matafonov, Anton, Sun, Mao-fu, Cheng, Qiufang, Dickeson, S. Kent, Verhamme, Ingrid M., Emsley, Jonas, Gailani, David
Format: Article
Published: American Society of Hematology 2017
Online Access:https://eprints.nottingham.ac.uk/44922/
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author Ivanov, Ivan
Matafonov, Anton
Sun, Mao-fu
Cheng, Qiufang
Dickeson, S. Kent
Verhamme, Ingrid M.
Emsley, Jonas
Gailani, David
author_facet Ivanov, Ivan
Matafonov, Anton
Sun, Mao-fu
Cheng, Qiufang
Dickeson, S. Kent
Verhamme, Ingrid M.
Emsley, Jonas
Gailani, David
author_sort Ivanov, Ivan
building Nottingham Research Data Repository
collection Online Access
description When blood is exposed to variety of artificial surfaces and biologic substances, the plasma proteins factor XII (FXII) and prekallikrein undergo reciprocal proteolytic conversion to the proteases αFXIIa and α-kallikrein by a process called contact activation. These enzymes contribute to host-defense responses including coagulation, inflammation, and fibrinolysis. The initiating event in contact activation is debated. To test the hypothesis that single-chain FXII expresses activity that could initiate contact activation, we prepared human FXII variants lacking the Arg353 cleavage site required for conversion to αFXIIa (FXII-R353A), or lacking the 3 known cleavage sites at Arg334, Arg343, and Arg353 (FXII-T, for “triple” mutant), and compared their properties to wild-type αFXIIa. In the absence of a surface, FXII-R353A and FXII-T activate prekallikrein and cleave the tripeptide S-2302, demonstrating proteolytic activity. The activity is several orders of magnitude weaker than that of αFXIIa. Polyphosphate, an inducer of contact activation, enhances PK activation by FXII-T, and facilitates FXII-T activation of FXII and FXI. In plasma, FXII-T and FXII-R353A, but not FXII lacking the active site serine residue (FXII-S544A), shortened the clotting time of FXII-deficient plasma and enhanced thrombin generation in a surface-dependent manner. The effect was not as strong as for wild-type FXII. Our results support a model for induction of contact activation in which activity intrinsic to single-chain FXII initiates αFXIIa and α-kallikrein formation on a surface. αFXIIa, with support from α-kallikrein, subsequently accelerates contact activation and is responsible for the full procoagulant activity of FXII.
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spelling nottingham-449222020-05-04T18:38:09Z https://eprints.nottingham.ac.uk/44922/ Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation Ivanov, Ivan Matafonov, Anton Sun, Mao-fu Cheng, Qiufang Dickeson, S. Kent Verhamme, Ingrid M. Emsley, Jonas Gailani, David When blood is exposed to variety of artificial surfaces and biologic substances, the plasma proteins factor XII (FXII) and prekallikrein undergo reciprocal proteolytic conversion to the proteases αFXIIa and α-kallikrein by a process called contact activation. These enzymes contribute to host-defense responses including coagulation, inflammation, and fibrinolysis. The initiating event in contact activation is debated. To test the hypothesis that single-chain FXII expresses activity that could initiate contact activation, we prepared human FXII variants lacking the Arg353 cleavage site required for conversion to αFXIIa (FXII-R353A), or lacking the 3 known cleavage sites at Arg334, Arg343, and Arg353 (FXII-T, for “triple” mutant), and compared their properties to wild-type αFXIIa. In the absence of a surface, FXII-R353A and FXII-T activate prekallikrein and cleave the tripeptide S-2302, demonstrating proteolytic activity. The activity is several orders of magnitude weaker than that of αFXIIa. Polyphosphate, an inducer of contact activation, enhances PK activation by FXII-T, and facilitates FXII-T activation of FXII and FXI. In plasma, FXII-T and FXII-R353A, but not FXII lacking the active site serine residue (FXII-S544A), shortened the clotting time of FXII-deficient plasma and enhanced thrombin generation in a surface-dependent manner. The effect was not as strong as for wild-type FXII. Our results support a model for induction of contact activation in which activity intrinsic to single-chain FXII initiates αFXIIa and α-kallikrein formation on a surface. αFXIIa, with support from α-kallikrein, subsequently accelerates contact activation and is responsible for the full procoagulant activity of FXII. American Society of Hematology 2017-03-16 Article PeerReviewed Ivanov, Ivan, Matafonov, Anton, Sun, Mao-fu, Cheng, Qiufang, Dickeson, S. Kent, Verhamme, Ingrid M., Emsley, Jonas and Gailani, David (2017) Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation. Blood, 129 . pp. 1527-1537. ISSN 1528-0020 http://www.bloodjournal.org/content/129/11/1527 doi:10.1182/blood-2016-10-744110 doi:10.1182/blood-2016-10-744110
spellingShingle Ivanov, Ivan
Matafonov, Anton
Sun, Mao-fu
Cheng, Qiufang
Dickeson, S. Kent
Verhamme, Ingrid M.
Emsley, Jonas
Gailani, David
Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation
title Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation
title_full Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation
title_fullStr Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation
title_full_unstemmed Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation
title_short Proteolytic properties of single-chain factor XII: a mechanism for triggering contact activation
title_sort proteolytic properties of single-chain factor xii: a mechanism for triggering contact activation
url https://eprints.nottingham.ac.uk/44922/
https://eprints.nottingham.ac.uk/44922/
https://eprints.nottingham.ac.uk/44922/