Unfoldomics of human diseases: linking protein intrinsic disorder with diseases

被引:214
作者
Uversky, Vladimir N. [1 ,2 ,3 ]
Oldfield, Christopher J. [1 ]
Midic, Uros [4 ]
Xie, Hongbo [4 ]
Xue, Bin [1 ,2 ]
Vucetic, Slobodan [4 ]
Iakoucheva, Lilia M. [5 ]
Obradovic, Zoran [4 ]
Dunker, A. Keith [1 ]
机构
[1] Indiana Univ, Sch Med, Ctr Computat Biol & Bioinformat, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Inst Intrinsically Disordered Prot Res, Indianapolis, IN 46202 USA
[3] Russian Acad Sci, Inst Biol Instrumentat, Pushchino 142290, Moscow Region, Russia
[4] Temple Univ, Ctr Informat Sci & Technol, Philadelphia, PA 19122 USA
[5] Rockefeller Univ, Lab Stat Genet, New York, NY 10065 USA
来源
BMC GENOMICS | 2009年 / 10卷
关键词
NATIVELY UNFOLDED PROTEINS; MOLTEN GLOBULE STATE; RNA-BINDING PROTEIN; UNSTRUCTURED PROTEINS; ALPHA-SYNUCLEIN; FUNCTIONAL ANTHOLOGY; PARKINSONS-DISEASE; HUB PROTEINS; NEURODEGENERATIVE DISEASES; STRUCTURE PREDICTION;
D O I
10.1186/1471-2164-10-S1-S7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Intrinsically disordered proteins (IDPs) and intrinsically disordered regions (IDRs) lack stable tertiary and/or secondary structure yet fulfills key biological functions. The recent recognition of IDPs and IDRs is leading to an entire field aimed at their systematic structural characterization and at determination of their mechanisms of action. Bioinformatics studies showed that IDPs and IDRs are highly abundant in different proteomes and carry out mostly regulatory functions related to molecular recognition and signal transduction. These activities complement the functions of structured proteins. IDPs and IDRs were shown to participate in both one-to-many and many-to-one signaling. Alternative splicing and posttranslational modifications are frequently used to tune the IDP functionality. Several individual IDPs were shown to be associated with human diseases, such as cancer, cardiovascular disease, amyloidoses, diabetes, neurodegenerative diseases, and others. This raises questions regarding the involvement of IDPs and IDRs in various diseases. Results: IDPs and IDRs were shown to be highly abundant in proteins associated with various human maladies. As the number of IDPs related to various diseases was found to be very large, the concepts of the disease-related unfoldome and unfoldomics were introduced. Novel bioinformatics tools were proposed to populate and characterize the disease-associated unfoldome. Structural characterization of the members of the disease-related unfoldome requires specialized experimental approaches. IDPs possess a number of unique structural and functional features that determine their broad involvement into the pathogenesis of various diseases. Conclusion: Proteins associated with various human diseases are enriched in intrinsic disorder. These disease-associated IDPs and IDRs are real, abundant, diversified, vital, and dynamic. These proteins and regions comprise the disease-related unfoldome, which covers a significant part of the human proteome. Profound association between intrinsic disorder and various human diseases is determined by a set of unique structural and functional characteristics of IDPs and IDRs. Unfoldomics of human diseases utilizes unrivaled bioinformatics and experimental techniques, paves the road for better understanding of human diseases, their pathogenesis and molecular mechanisms, and helps develop new strategies for the analysis of disease-related proteins.
引用
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页数:17
相关论文
共 117 条
[51]   The PSIPRED protein structure prediction server [J].
McGuffin, LJ ;
Bryson, K ;
Jones, DT .
BIOINFORMATICS, 2000, 16 (04) :404-405
[52]  
McMeekin T., 1952, Journal of Food Protection, V15, P57
[53]   Protein disorder in the human diseasome: unfoldomics of human genetic diseases [J].
Midic, Uros ;
Oldfield, Christopher J. ;
Dunker, A. Keith ;
Obradovic, Zoran ;
Uversky, Vladimir N. .
BMC GENOMICS, 2009, 10
[54]   On the structure of native, denatured, and coagulated proteins [J].
Mirsky, AE ;
Pauling, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1936, 22 :439-447
[55]   Predicting intrinsic disorder from amino acid sequence [J].
Obradovic, Z ;
Peng, K ;
Vucetic, S ;
Radivojac, P ;
Brown, CJ ;
Dunker, AK .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 2003, 53 (06) :566-572
[56]   Exploiting heterogeneous sequence properties improves prediction of protein disorder [J].
Obradovic, Z ;
Peng, K ;
Vucetic, S ;
Radivojac, P ;
Dunker, AK .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2005, 61 :176-182
[57]   Flexible nets: disorder and induced fit in the associations of p53 and 14-3-3 with their partners [J].
Oldfield, Christopher J. ;
Meng, Jingwei ;
Yang, Jack Y. ;
Yang, Mary Qu ;
Uversky, Vladimir N. ;
Dunker, A. Keith .
BMC GENOMICS, 2008, 9 (Suppl 1)
[58]   Coupled folding and binding with α-helix-forming molecular recognition elements [J].
Oldfield, CJ ;
Cheng, YG ;
Cortese, MS ;
Romero, P ;
Uversky, VN ;
Dunker, AK .
BIOCHEMISTRY, 2005, 44 (37) :12454-12470
[59]   Comparing and combining predictors of mostly disordered proteins [J].
Oldfield, CJ ;
Cheng, Y ;
Cortese, MS ;
Brown, CJ ;
Uversky, VN ;
Dunker, AK .
BIOCHEMISTRY, 2005, 44 (06) :1989-2000
[60]   ONCOPROTEIN MDM2 CONCEALS THE ACTIVATION DOMAIN OF TUMOR SUPPRESSOR-P53 [J].
OLINER, JD ;
PIETENPOL, JA ;
THIAGALINGAM, S ;
GVURIS, J ;
KINZLER, KW ;
VOGELSTEIN, B .
NATURE, 1993, 362 (6423) :857-860