Home LiteratureArticle Details
PMID: 12673016 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Two regions responsible for the actin binding of p57, a mammalian coronin family actin-binding protein.

Biological & pharmaceutical bulletin ·Vol. 26 ·No. 4 ·2003-04-00 ·Pages 409-16

Oku T, Itoh S, Okano M, Suzuki A, Suzuki K, Nakajin S, Tsuji T, Nauseef WM, Toyoshima S

Abstract

The actin-binding protein p57, a member of the coronin protein family, is expressed in a variety of immune cells. It has five WD repeats and a coiled-coil motif containing a leucine zipper, both of which are known to mediate protein-protein interactions. In order to identify the precise actin-binding regions in p57, and to assess the contribution of these structural motifs, we prepared various truncated p57 as fusion proteins with glutathione S-transferase (GST) and examined their actin-binding activity. A co-sedimentation assay demonstrated that p57(1-371) (C-terminal truncated p57) had the ability to bind F-actin, but p57(372-461) (a fragment containing the coiled-coil motif) did not. A segment consisting of the N-terminal 34 amino acids of p57 (p57(1-34)) was found to bind to F-actin in the co-sedimentation assay. Furthermore, fluorescence microscopic observation showed that p57(1-34) was co-localized with F-actin in COS-1 cells after the transfection with the p57(1-34) construct. Deletion of (10)KFRHVF(15), a sequence conserved among coronin-related proteins, from p57(1-34) abolished its actin-binding activity, suggesting that this sequence with basic and hydrophobic amino acids is crucial for p57 to bind to F-actin. However, the N-terminal deletion mutant p57(63-461) retained the binding ability to F-actin. This result suggests the presence of a second actin-binding region. Further deletion analysis revealed that p57(111-204), which includes the second and third WD repeats, also exhibited weak actin-binding activity in the co-sedimentation assay. Taken together, these data strongly suggest that at least two regions within Met-1 to Asp-34 and Ile-111 to Glu-204 of p57 are responsible for its binding to the actin cytoskeleton.

MeSH Terms
Actins/genetics,metabolism Amino Acid Sequence Animals Binding Sites COS Cells Chlorocebus aethiops Microfilament Proteins/genetics,metabolism Molecular Sequence Data Polypyrimidine Tract-Binding Protein/genetics,metabolism Protein Binding
Chemicals
Actins Microfilament Proteins Polypyrimidine Tract-Binding Protein coronin proteins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Oku Teruaki
Hoshi University School of Pharmacy and Pharmaceutical Sciences, Tokyo, Japan.
Itoh Saotomo
Okano Masamitsu
Suzuki Akiko
Suzuki Kensuke
Nakajin Shizuo
Tsuji Tsutomu
Nauseef William Michael
Toyoshima Satoshi
Article Info
Journal
Biological & pharmaceutical bulletin
Abbr.
Biol Pharm Bull
ISSN
0918-6158
Published
2003-04-00
Pages
409-16
Language
English
Region
Japan
NLM ID
9311984
Subset
IM
Grants
BLRD VA · I01 BX000513 · United States
NIAID NIH HHS · R01AI34879 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com