A Common Amino Acid Sequence in 190-kDa Microtubule-associated Protein and Tau for the Promotion of Microtubule Assembly
Previously we reported that chymotryptic fragments of bovine adrenal 190-kDa microtubule-associated proteins (27-kDa fragment) and bovine brain tau (14-kDa fragment) contained microtubule-binding domain (Aizawa, H., Murofushi, H., Kotani, Hisanaga, S., Hirokawa, N., and Sakai, H. (1987) J. Biol. Che...
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description | Previously we reported that chymotryptic fragments of bovine adrenal 190-kDa microtubule-associated proteins (27-kDa fragment) and bovine brain tau (14-kDa fragment) contained microtubule-binding domain (Aizawa, H., Murofushi, H., Kotani, Hisanaga, S., Hirokawa, N., and Sakai, H. (1987) J. Biol. Chem. 262, 3782–3787; Aizawa, H., Kawasaki, H., Murofushi, H., Kotani, S., Suzuki, K., and Sakai, H. (1988) J. Biol. Chem. 263, 7703–7707). In order to study the structure of microtubule-binding domain of the two microtubule-associated proteins, we analyzed the amino acid sequence of the 27-kDa fragment and compared the sequence with that of the 14-kDa fragment. This revealed that 190-kDa microtubule-associated protein and tau contained at least one common sequence of 20 amino acid residues in their microtubule-binding domains. A synthetic polypeptide corresponding to the common sequence (Lys-Asn-Val-Arg-Ser-Lys-Val-Gly-Ser-Thr-Glu-Asn-Ile-Lys- His-Gln-Pro-Gly-Gly-Gly-Arg-Ala-Lys) was bound to microtubules competitively with the 190-kDa MAP. The apparent dissociation constant (KD) for the binding of the polypeptide to microtubules was estimated to be 1.8 × 10−4M, and the maximum binding reached 1.2 mol of the synthetic polypeptide/mol of tubulin dimer. This synthetic polypeptide increased the rate and extent of tubulin polymerization and decreased the critical concentration of tubulin for polymerization. The polypeptide-induced tubulin polymers were morphologically normal microtubules and were disassembled by cold treatment. The common sequence (termed assembly-promoting sequence) was thus identified as the active site of 190-kDa microtubule-associated protein and tau for the promotion of microtubule assembly. The reconstitution system of microtubules with this synthetic polypeptide with assembly-promoting sequence may be useful to elucidate detailed molecular mechanism of the promotion of microtubule assembly by microtubule-associated proteins. |
doi_str_mv | 10.1016/S0021-9258(18)83632-8 |
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(1987) J. Biol. Chem. 262, 3782–3787; Aizawa, H., Kawasaki, H., Murofushi, H., Kotani, S., Suzuki, K., and Sakai, H. (1988) J. Biol. Chem. 263, 7703–7707). In order to study the structure of microtubule-binding domain of the two microtubule-associated proteins, we analyzed the amino acid sequence of the 27-kDa fragment and compared the sequence with that of the 14-kDa fragment. This revealed that 190-kDa microtubule-associated protein and tau contained at least one common sequence of 20 amino acid residues in their microtubule-binding domains. A synthetic polypeptide corresponding to the common sequence (Lys-Asn-Val-Arg-Ser-Lys-Val-Gly-Ser-Thr-Glu-Asn-Ile-Lys- His-Gln-Pro-Gly-Gly-Gly-Arg-Ala-Lys) was bound to microtubules competitively with the 190-kDa MAP. The apparent dissociation constant (KD) for the binding of the polypeptide to microtubules was estimated to be 1.8 × 10−4M, and the maximum binding reached 1.2 mol of the synthetic polypeptide/mol of tubulin dimer. This synthetic polypeptide increased the rate and extent of tubulin polymerization and decreased the critical concentration of tubulin for polymerization. The polypeptide-induced tubulin polymers were morphologically normal microtubules and were disassembled by cold treatment. The common sequence (termed assembly-promoting sequence) was thus identified as the active site of 190-kDa microtubule-associated protein and tau for the promotion of microtubule assembly. The reconstitution system of microtubules with this synthetic polypeptide with assembly-promoting sequence may be useful to elucidate detailed molecular mechanism of the promotion of microtubule assembly by microtubule-associated proteins.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(18)83632-8</identifier><identifier>PMID: 2494169</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Adrenal Glands - metabolism ; Amino Acid Sequence ; Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; Brain - metabolism ; Cattle ; Fundamental and applied biological sciences. Psychology ; Holoproteins ; Microtubule-Associated Proteins - genetics ; Microtubule-Associated Proteins - metabolism ; microtubules ; Microtubules - metabolism ; Microtubules - ultrastructure ; Molecular Sequence Data ; Molecular Weight ; Nerve Tissue Proteins - genetics ; Other proteins ; Peptide Fragments - isolation & purification ; Peptide Fragments - metabolism ; Proteins ; tau Proteins</subject><ispartof>The Journal of biological chemistry, 1989-04, Vol.264 (10), p.5885-5890</ispartof><rights>1989 © 1989 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c561t-d8f59d89707c2d60e02d879e030efee05e5c6a9fa8e2a8e7ec8ad4a787e7cd6c3</citedby><cites>FETCH-LOGICAL-c561t-d8f59d89707c2d60e02d879e030efee05e5c6a9fa8e2a8e7ec8ad4a787e7cd6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7311716$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2494169$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aizawa, H</creatorcontrib><creatorcontrib>Kawasaki, H</creatorcontrib><creatorcontrib>Murofushi, H</creatorcontrib><creatorcontrib>Kotani, S</creatorcontrib><creatorcontrib>Suzuki, K</creatorcontrib><creatorcontrib>Sakai, H</creatorcontrib><title>A Common Amino Acid Sequence in 190-kDa Microtubule-associated Protein and Tau for the Promotion of Microtubule Assembly</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Previously we reported that chymotryptic fragments of bovine adrenal 190-kDa microtubule-associated proteins (27-kDa fragment) and bovine brain tau (14-kDa fragment) contained microtubule-binding domain (Aizawa, H., Murofushi, H., Kotani, Hisanaga, S., Hirokawa, N., and Sakai, H. (1987) J. Biol. Chem. 262, 3782–3787; Aizawa, H., Kawasaki, H., Murofushi, H., Kotani, S., Suzuki, K., and Sakai, H. (1988) J. Biol. Chem. 263, 7703–7707). In order to study the structure of microtubule-binding domain of the two microtubule-associated proteins, we analyzed the amino acid sequence of the 27-kDa fragment and compared the sequence with that of the 14-kDa fragment. This revealed that 190-kDa microtubule-associated protein and tau contained at least one common sequence of 20 amino acid residues in their microtubule-binding domains. A synthetic polypeptide corresponding to the common sequence (Lys-Asn-Val-Arg-Ser-Lys-Val-Gly-Ser-Thr-Glu-Asn-Ile-Lys- His-Gln-Pro-Gly-Gly-Gly-Arg-Ala-Lys) was bound to microtubules competitively with the 190-kDa MAP. The apparent dissociation constant (KD) for the binding of the polypeptide to microtubules was estimated to be 1.8 × 10−4M, and the maximum binding reached 1.2 mol of the synthetic polypeptide/mol of tubulin dimer. This synthetic polypeptide increased the rate and extent of tubulin polymerization and decreased the critical concentration of tubulin for polymerization. The polypeptide-induced tubulin polymers were morphologically normal microtubules and were disassembled by cold treatment. The common sequence (termed assembly-promoting sequence) was thus identified as the active site of 190-kDa microtubule-associated protein and tau for the promotion of microtubule assembly. The reconstitution system of microtubules with this synthetic polypeptide with assembly-promoting sequence may be useful to elucidate detailed molecular mechanism of the promotion of microtubule assembly by microtubule-associated proteins.</description><subject>Adrenal Glands - metabolism</subject><subject>Amino Acid Sequence</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - metabolism</subject><subject>Cattle</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Holoproteins</subject><subject>Microtubule-Associated Proteins - genetics</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>microtubules</subject><subject>Microtubules - metabolism</subject><subject>Microtubules - ultrastructure</subject><subject>Molecular Sequence Data</subject><subject>Molecular Weight</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Other proteins</subject><subject>Peptide Fragments - isolation & purification</subject><subject>Peptide Fragments - metabolism</subject><subject>Proteins</subject><subject>tau Proteins</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkW1rFDEQx4Mo9Xr6EQoBRfTFarLZPL0qy_kIFYVW8F3IJbNedHdTk11rv73Z3nH4roFkYOY3k5n5I3RGyWtKqHhzSUhNK11z9ZKqV4oJVlfqAVpRoljFOP3-EK2OyGN0mvNPUk6j6Qk6qRvdUKFX6G-LN3EY4ojbIYwRty54fAm_Zxgd4DBiqkn1663Fn4NLcZq3cw-VzTm6YCfw-GtxQsHs6PGVnXEXE552sPiHOIVSN3b_5-I2Zxi2_e0T9KizfYanB7tG396_u9p8rC6-fPi0aS8qxwWdKq86rr3SkkhXe0GA1F5JDYQR6AAIB-6E1Z1VUJcrwSnrGyuVBOm8cGyNXuzrXqdYpsqTGUJ20Pd2hDhnI5Uq1VVzL0g5q5kWrIB8D5ahck7QmesUBptuDSVmkcbcSWOWvRuqzJ005V2js8MH83YAf8w6aFHizw9xm53tu2RHF_IRk4xSSUXBnu2xXfixuwkJzDZEt4PB1KJZWuBK8UKd7ykou_0TIJnswqKpLxluMj6Ge9r9B1vptsw</recordid><startdate>19890405</startdate><enddate>19890405</enddate><creator>Aizawa, H</creator><creator>Kawasaki, H</creator><creator>Murofushi, H</creator><creator>Kotani, S</creator><creator>Suzuki, K</creator><creator>Sakai, H</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M81</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19890405</creationdate><title>A Common Amino Acid Sequence in 190-kDa Microtubule-associated Protein and Tau for the Promotion of Microtubule Assembly</title><author>Aizawa, H ; Kawasaki, H ; Murofushi, H ; Kotani, S ; Suzuki, K ; Sakai, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c561t-d8f59d89707c2d60e02d879e030efee05e5c6a9fa8e2a8e7ec8ad4a787e7cd6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adrenal Glands - metabolism</topic><topic>Amino Acid Sequence</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - metabolism</topic><topic>Cattle</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Holoproteins</topic><topic>Microtubule-Associated Proteins - genetics</topic><topic>Microtubule-Associated Proteins - metabolism</topic><topic>microtubules</topic><topic>Microtubules - metabolism</topic><topic>Microtubules - ultrastructure</topic><topic>Molecular Sequence Data</topic><topic>Molecular Weight</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Other proteins</topic><topic>Peptide Fragments - isolation & purification</topic><topic>Peptide Fragments - metabolism</topic><topic>Proteins</topic><topic>tau Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aizawa, H</creatorcontrib><creatorcontrib>Kawasaki, H</creatorcontrib><creatorcontrib>Murofushi, H</creatorcontrib><creatorcontrib>Kotani, S</creatorcontrib><creatorcontrib>Suzuki, K</creatorcontrib><creatorcontrib>Sakai, H</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 3</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aizawa, H</au><au>Kawasaki, H</au><au>Murofushi, H</au><au>Kotani, S</au><au>Suzuki, K</au><au>Sakai, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Common Amino Acid Sequence in 190-kDa Microtubule-associated Protein and Tau for the Promotion of Microtubule Assembly</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1989-04-05</date><risdate>1989</risdate><volume>264</volume><issue>10</issue><spage>5885</spage><epage>5890</epage><pages>5885-5890</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>Previously we reported that chymotryptic fragments of bovine adrenal 190-kDa microtubule-associated proteins (27-kDa fragment) and bovine brain tau (14-kDa fragment) contained microtubule-binding domain (Aizawa, H., Murofushi, H., Kotani, Hisanaga, S., Hirokawa, N., and Sakai, H. (1987) J. Biol. Chem. 262, 3782–3787; Aizawa, H., Kawasaki, H., Murofushi, H., Kotani, S., Suzuki, K., and Sakai, H. (1988) J. Biol. Chem. 263, 7703–7707). In order to study the structure of microtubule-binding domain of the two microtubule-associated proteins, we analyzed the amino acid sequence of the 27-kDa fragment and compared the sequence with that of the 14-kDa fragment. This revealed that 190-kDa microtubule-associated protein and tau contained at least one common sequence of 20 amino acid residues in their microtubule-binding domains. A synthetic polypeptide corresponding to the common sequence (Lys-Asn-Val-Arg-Ser-Lys-Val-Gly-Ser-Thr-Glu-Asn-Ile-Lys- His-Gln-Pro-Gly-Gly-Gly-Arg-Ala-Lys) was bound to microtubules competitively with the 190-kDa MAP. The apparent dissociation constant (KD) for the binding of the polypeptide to microtubules was estimated to be 1.8 × 10−4M, and the maximum binding reached 1.2 mol of the synthetic polypeptide/mol of tubulin dimer. This synthetic polypeptide increased the rate and extent of tubulin polymerization and decreased the critical concentration of tubulin for polymerization. The polypeptide-induced tubulin polymers were morphologically normal microtubules and were disassembled by cold treatment. The common sequence (termed assembly-promoting sequence) was thus identified as the active site of 190-kDa microtubule-associated protein and tau for the promotion of microtubule assembly. The reconstitution system of microtubules with this synthetic polypeptide with assembly-promoting sequence may be useful to elucidate detailed molecular mechanism of the promotion of microtubule assembly by microtubule-associated proteins.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>2494169</pmid><doi>10.1016/S0021-9258(18)83632-8</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal Glands - metabolism Amino Acid Sequence Analytical, structural and metabolic biochemistry Animals Biological and medical sciences Brain - metabolism Cattle Fundamental and applied biological sciences. Psychology Holoproteins Microtubule-Associated Proteins - genetics Microtubule-Associated Proteins - metabolism microtubules Microtubules - metabolism Microtubules - ultrastructure Molecular Sequence Data Molecular Weight Nerve Tissue Proteins - genetics Other proteins Peptide Fragments - isolation & purification Peptide Fragments - metabolism Proteins tau Proteins |
title | A Common Amino Acid Sequence in 190-kDa Microtubule-associated Protein and Tau for the Promotion of Microtubule Assembly |
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