Conformation of polypyrimidine tract binding protein in solution

被引:55
作者
Petoukhov, Maxim V.
Monie, Tom P.
Allain, Frederic H. -T.
Matthews, Stephen
Curry, Stephen
Svergun, Dmitri I.
机构
[1] Hamburg Outstn, European Mol Biol Lab, D-22603 Hamburg, Germany
[2] Russian Acad Sci, Inst Crystallog, Moscow 117333, Russia
[3] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Biol, London SW7 2AZ, England
[4] Univ London Imperial Coll Sci Technol & Med, Div Mol Biosci, London SW7 2AZ, England
[5] ETH Honggerberg, Swiss Fed Inst Technol, Dept Biol, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
基金
英国惠康基金;
关键词
D O I
10.1016/j.str.2006.04.005
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
The polypyrimidine tract binding protein (PTB) is an RNA binding protein that normally functions as a regulator of alternative splicing but can also be recruited to stimulate translation initiation by certain picornaviruses. High-resolution structures of the four RNA recognition motifs (RRMs) that make up PTB have previously been determined by NMR. Here, we have used small-angle X-ray scattering to determine the low-resolution structure of the entire protein. Scattering patterns from full-length PTB and deletion mutants containing all possible sequential combinations of the RRMs were collected. All constructs were found to be monomeric in solution. Ab initio analysis and rigid-body modeling utilizing the high-resolution models of the RRMs yielded a consistent low-resolution model of the spatial organization of domains in PTB. Domains 3 and 4 were found to be in close contact, whereas domains 2 and especially 1 had loose contacts with the rest of the protein.
引用
收藏
页码:1021 / 1027
页数:7
相关论文
共 39 条
[1]   Exon repression by polypyrimidine tract binding protein [J].
Amir-Ahmady, B ;
Boutz, PL ;
Markovtsov, V ;
Phillips, ML ;
Black, DL .
RNA, 2005, 11 (05) :699-716
[2]   DATA ACQUISITION-SYSTEMS FOR LINEAR AND AREA X-RAY-DETECTORS USING DELAY-LINE READOUT [J].
BOULIN, CJ ;
KEMPF, R ;
GABRIEL, A ;
KOCH, MHJ .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 1988, 269 (01) :312-320
[3]   The polypyrimidine tract binding protein binds upstream of neural cell-specific c-src exon N1 to repress the splicing of the intron downstream [J].
Chan, RCC ;
Black, DL .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (08) :4667-4676
[4]   Multisite RNA binding and release of polypyrimidine tract binding protein during the regulation of c-src neural-specific splicing [J].
Chou, MY ;
Underwood, JG ;
Nikolic, J ;
Luu, MHT ;
Black, DL .
MOLECULAR CELL, 2000, 5 (06) :949-957
[5]   Structure of tandem RNA recognition motifs from polypyrimidine tract binding protein reveals novel features of the RRM fold [J].
Conte, MR ;
Grüne, T ;
Ghuman, J ;
Kelly, G ;
Ladas, A ;
Matthews, S ;
Curry, S .
EMBO JOURNAL, 2000, 19 (12) :3132-3141
[6]   A Xenopus protein related to hnRNP I has a role in cytoplasmic RNA localization [J].
Cote, CA ;
Gautreau, D ;
Denegre, JM ;
Kress, TL ;
Terry, NA ;
Mowry, KL .
MOLECULAR CELL, 1999, 4 (03) :431-437
[7]   40LoVe interacts with Vg1RBP/Vera and hnRNP I in binding the Vg1-Localization Element [J].
Czaplinski, K ;
Mattaj, IW .
RNA, 2006, 12 (02) :213-222
[8]  
Feigin L., 1987, STRUCTURE ANAL SMALL
[9]   THE LOCALIZATION METHOD USED AT EMBL [J].
GABRIEL, A ;
DAUVERGNE, F .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH, 1982, 201 (01) :223-224
[10]  
Guinier A., 1939, Ann Phys, V12, P161, DOI DOI 10.1051/ANPHYS/193911120161