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Suh, Pann-Ghill
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dc.citation.endPage 28260 -
dc.citation.number 30 -
dc.citation.startPage 28252 -
dc.citation.title JOURNAL OF BIOLOGICAL CHEMISTRY -
dc.citation.volume 276 -
dc.contributor.author Lee, Sukmook -
dc.contributor.author Park, Jong Bae -
dc.contributor.author Kim, Jong Hyun -
dc.contributor.author Kim, Yong -
dc.contributor.author Kim, Jung Hwan -
dc.contributor.author Shin, Kum-Joo -
dc.contributor.author Lee, Jun Sung -
dc.contributor.author Ha, Sang Hoon -
dc.contributor.author Suh, Pann-Ghill -
dc.contributor.author Ryu, Sung Ho -
dc.date.accessioned 2023-12-22T11:43:24Z -
dc.date.available 2023-12-22T11:43:24Z -
dc.date.created 2015-08-13 -
dc.date.issued 2001-07 -
dc.description.abstract Mammalian phospholipase D (PLD) plays a key role in several signal transduction pathways and is involved in many diverse functions. To elucidate the complex molecular regulation of PLD, we investigated PLD-binding proteins obtained from rat brain extract. Here we report that a 43-kDa protein in the rat brain, beta -actin, acts as a major PLD2 direct-binding protein as revealed by peptide mass fingerprinting in combination with matrix-assisted laser desorption ionization time-of-flight mass spectrometry. We also determined that the region between amino acids 613 and 723 of PLD2 is required for the direct binding of beta -actin, using bacterially expressed glutathione S-transferase fusion proteins of PLD2 fragments. Intriguingly, purified beta -actin potently inhibited both phosphaticlylinositol-4,5-bisphosphate and oleate-dependent PLD2 activities in a concentration-dependent manner (IC50 = 5 nM). In a previous paper, we reported that alpha -actinin inhibited PLD2 activity in an interaction-dependent and an ADP-ribosylation factor 1 (ARF1)-reversible manner (Park, J. B., Kim, J. H., Kim, Y., Ha, S. H., Kim, J. H., Yoo, J.-S., Du, G., Frohman, M. A., Sub, P.-G., and Ryu, S. H. (2000) J. Biol. Chem. 275, 21295-21301). In vitro binding analyses showed that beta -actin could displace alpha -actinin binding to PLD2, demonstrating independent interaction between cytoskeletal proteins and PLD2. Furthermore, ARF1 could steer the PLD2 activity in a positive direction regardless of the inhibitory effect of beta -actin on PLD2. We also observed that beta -actin regulates PLD1 and PLD2 with similar binding and inhibitory potencies. Immunocytochemical. and co-immunoprecipitation studies demonstrated the in vivo interaction between the two PLD isozymes and actin in cells. Taken together, these results suggest that the regulation of PLD by cytoskeletal proteins, beta -actin and a-actinin, and ARF1 may play an important role in cytoskeleton-related PLD functions -
dc.identifier.bibliographicCitation JOURNAL OF BIOLOGICAL CHEMISTRY, v.276, no.30, pp.28252 - 28260 -
dc.identifier.doi 10.1074/jbc.M008521200 -
dc.identifier.issn 0021-9258 -
dc.identifier.scopusid 2-s2.0-0035958955 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/16523 -
dc.identifier.url http://www.jbc.org/content/276/30/28252.long -
dc.identifier.wosid 000170093400069 -
dc.language 영어 -
dc.publisher AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC -
dc.title Actin directly interacts with phospholipase D, inhibiting its activity -
dc.type Article -
dc.description.journalRegisteredClass scopus -

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