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Binding of βγ subunits of heterotrimeric G proteins to the PH domain of Bruton tyrosine kinase

Tsukada, Satoshi and Simon, Melvin I. and Witte, Owen N. and Katz, Arieh (1994) Binding of βγ subunits of heterotrimeric G proteins to the PH domain of Bruton tyrosine kinase. Proceedings of the National Academy of Sciences of the United States of America, 91 (23). pp. 11256-11260. ISSN 0027-8424. http://resolver.caltech.edu/CaltechAUTHORS:20120221-155117939

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Abstract

Bruton tyrosine kinase (Btk) has been implicated as the defective gene in both human and murine B-cell deficiencies. The identification of molecules that interact with Btk may shed light on critical processes in lymphocyte development. The N-terminal unique region of Btk contains a pleckstrin homology domain. This domain is found in a broad array of signaling molecules and implicated to function in protein-protein interactions. By using an in vitro binding assay and an in vivo competition assay, the pleckstrin homology domain of Btk was shown to interact with the βγ dimer of heterotrimeric guanine nucleotide-binding proteins (G proteins). A highly conserved tryptophan residue in subdomain 6 of the pleckstrin homology domain was shown to play a critical role in the binding. The interaction of Btk with βγ suggests the existence of a unique connection between cytoplasmic tyrosine kinases and G proteins in cellular signal transduction.


Item Type:Article
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http://www.pnas.org/content/91/23/11256PublisherUNSPECIFIED
Additional Information:© 1994 National Academy of Sciences. Contributed by Melvin I. Simon, July 25, 1994. We thank Yuko Kawakami and Toshiaki Kawakami for helpful discussions. We thank Dr. Robert J. Lefkowitz for his generous gift of the DNA construct encoding the C-terminal 222 aa of βARK1 fused to GST and Julia Shimaoka for preparation of the manuscript. O.N.W. is an Investigator with the Howard Hughes Medical Institute. This work was supported by the Howard Hughes Medical Institute and National Institutes of Health Grant CA12800 to O.N.W. and by National Institutes of Health Grant GM 34236 to M.I.S. The publication costs of this article were defrayed in part by page charge payment. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.
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Funding AgencyGrant Number
Howard Hughes Medical Institute (HHMI)UNSPECIFIED
NIHCA12800
NIHGM 34236
Record Number:CaltechAUTHORS:20120221-155117939
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:20120221-155117939
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:29399
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:22 Feb 2012 00:19
Last Modified:26 Dec 2012 14:52

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