Cartilage acidic protein 1, a new member of the beta-propeller protein family with amyloid propensity

被引:19
作者
Anjos, Liliana [1 ,3 ]
Morgado, Isabel [1 ,3 ]
Guerreiro, Marta [1 ]
Cardoso, Joao C. R. [1 ]
Melo, Eduardo P. [2 ]
Power, Deborah M. [1 ,3 ]
机构
[1] Univ Algarve, Comparat Endocrinol & Integrat Biol Grp CEIB, Ctr Ciencias Mar CCMAR, Campus Gambelas, P-8005139 Faro, Portugal
[2] Univ Algarve, Ctr Biomed Res, Campus Gambelas, P-8005139 Faro, Portugal
[3] Boston Univ, Sch Med, Dept Physiol & Biophys, Boston, MA 02118 USA
关键词
cartilage acidic protein; extracellular matrix; teleost fish; protein evolution; amyloid; EPIDERMAL-GROWTH-FACTOR; MULTIPLE-SCLEROSIS; CONNECTIVITY PREDICTION; OLFACTOMEDIN DOMAIN; CRYSTAL-STRUCTURE; GENE-EXPRESSION; SEQUENCE; AGGREGATION; BIOMARKERS; MYOCILIN;
D O I
10.1002/prot.25210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cartilage acidic protein1 (CRTAC1) is an extracellular matrix protein of chondrogenic tissue in humans and its presence in bacteria indicate it is of ancient origin. Structural modeling of piscine CRTAC1 reveals it belongs to the large family of beta-propeller proteins that in mammals have been associated with diseases, including amyloid diseases such as Alzheimer's. In order to characterize the structure/function evolution of this new member of the beta-propeller family we exploited the unique characteristics of piscine duplicate genes Crtac1a and Crtac1b and compared their structural and biochemical modifications with human recombinant CRTAC1. We demonstrate that CRTAC1 has a beta-propeller structure that has been conserved during evolution and easily forms high molecular weight thermo-stable aggregates. We reveal for the first time the propensity of CRTAC1 to form amyloid-like structures, and hypothesize that the aggregating property of CRTAC1 may be related to its disease-association. We further contribute to the general understating of CRTAC1's and beta-propeller family evolution and function. Proteins 2017; 85:242-255. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:242 / 255
页数:14
相关论文
共 57 条
[1]   Disordered Flanks Prevent Peptide Aggregation [J].
Abeln, Sanne ;
Frenkel, Daan .
PLOS COMPUTATIONAL BIOLOGY, 2008, 4 (12)
[2]   Cartilage Acidic Protein 2 a hyperthermostable, high affinity calcium-binding protein [J].
Anjos, Liliana ;
Gomes, Ana S. ;
Melo, Eduardo P. ;
Canario, Adelino V. ;
Power, Deborah M. .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2013, 1834 (03) :642-650
[3]   Glomus Tumors in Neurofibromatosis Type 1: Genetic, Functional, and Clinical Evidence of a Novel Association [J].
Brems, Hilde ;
Park, Caroline ;
Maertens, Ophelia ;
Pemov, Alexander ;
Messia, Ludwine ;
Upadhyaya, Meena ;
Claes, Kathleen ;
Beert, Eline ;
Peeters, Kristel ;
Mautner, Victor ;
Sloan, Jennifer L. ;
Yao, Lawrence ;
Lee, Chyi-Chia Richard ;
Sciot, Raf ;
De Smet, Luc ;
Legius, Eric ;
Stewart, Douglas R. .
CANCER RESEARCH, 2009, 69 (18) :7393-7401
[4]   DISULFIND: a disulfide bonding state and cysteine connectivity prediction server [J].
Ceroni, Alessio ;
Passerini, Andrea ;
Vullo, Alessandro ;
Frasconi, Paolo .
NUCLEIC ACIDS RESEARCH, 2006, 34 :W177-W181
[5]   The many blades of the β-propeller proteins: conserved but versatile [J].
Chen, Cammy K. -M. ;
Chan, Nei-Li ;
Wang, Andrew H. -J. .
TRENDS IN BIOCHEMICAL SCIENCES, 2011, 36 (10) :553-561
[6]   Protein misfolding, functional amyloid, and human disease [J].
Chiti, Fabrizio ;
Dobson, Christopher M. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :333-366
[7]   β-propeller crystal structure of Psathyrella velutina lectin:: An integrin-like fungal protein interacting [J].
Cioci, G ;
Mitchell, EP ;
Chazalet, V ;
Debray, H ;
Oscarson, S ;
Lahmann, M ;
Gautier, C ;
Breton, C ;
Perez, S ;
Imberty, A .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 357 (05) :1575-1591
[8]   THE SOLUTION STRUCTURE OF HUMAN EPIDERMAL GROWTH-FACTOR [J].
COOKE, RM ;
WILKINSON, AJ ;
BARON, M ;
PASTORE, A ;
TAPPIN, MJ ;
CAMPBELL, ID ;
GREGORY, H ;
SHEARD, B .
NATURE, 1987, 327 (6120) :339-341
[9]   Solution structure of a pair of calcium-binding epidermal growth factor-like domains: Implications for the Marfan syndrome and other genetic disorders [J].
Downing, AK ;
Knott, V ;
Werner, JM ;
Cardy, CM ;
Campbell, ID ;
Handford, PA .
CELL, 1996, 85 (04) :597-605
[10]   DiANNA:: a web server for disulfide connectivity prediction [J].
Ferrè, F ;
Clote, P .
NUCLEIC ACIDS RESEARCH, 2005, 33 :W230-W232