Near-UV Circular Dichroism Reveals Structural Transitions of Vimentin Subunits during Intermediate Filament Assembly

被引:22
作者
Georgakopoulou, Sofia [1 ]
Moeller, Dorothee [2 ]
Sachs, Nadine [2 ]
Herrmann, Harald [2 ]
Aebi, Ueli [1 ]
机构
[1] Univ Basel, Biozentrum, ME Muller Inst Struct Biol, CH-4056 Basel, Switzerland
[2] German Canc Res Ctr, Div Mol Genet, D-69120 Heidelberg, Germany
基金
瑞士国家科学基金会;
关键词
intermediate filaments; circular dichroism; unit-length filaments; vimentin; MOLECULAR ARCHITECTURE; MICROTUBULE PROTEIN; PURPLE BACTERIA; BOVINE BRAIN; CONFORMATION; SPECTRA; TUBULIN; CD; COMPLEXES; DESMIN;
D O I
10.1016/j.jmb.2008.12.053
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
In vitro assembly of vimentin intermediate filaments (IFs) proceeds from soluble, reconstituted tetrameric complexes to mature filaments in three distinct stages: (1) within the first seconds after initiation of assembly, tetramers laterally associate into unit-length filaments (ULFs), on average 17 nm wide; (2) for the next few minutes, ULFs grow by longitudinal annealing into short, immature filaments; (3) almost concomitant with elongation, these immature filaments begin to radially compact, yielding similar to 11-nm-wide IFs at around 15 min. The near-UV CD signal Of Soluble tetramers exhibits two main peaks at 285 and 278 nm, which do not change during ULF formation. In contrast, the CD signal of mature IFs exhibits two major changes: (1) the 278-nm band, denoting the transition of the tyrosines from the ground state to the first vibrational mode of the excited state, is lost; (2) a red-shifted band appears at 291 nm, indicating the emergence of a new electronic species. These changes take place independently and at different time scales. The 278-nm signal disappears within the first minute of assembly, compatible with increased rigidity of the tyrosines during elongation of the ULFs. The rise of the 291-nm band has a lifetime of similar to 13 min and denotes the generation of phenolates by deprotonation of the tyrosines' hydroxyl group after they relocalize into a negatively charged environment. The appearance of such tyrosine-binding "pockets" in the assembling filaments highlights an essential part of the molecular rearrangements characterizing the later stages of the assembly process, including the radial compaction. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:544 / 553
页数:10
相关论文
共 45 条
[1]   UNIFYING PRINCIPLES IN INTERMEDIATE FILAMENT (IF) STRUCTURE AND ASSEMBLY [J].
AEBI, U ;
HANER, M ;
TRONCOSO, J ;
EICHNER, R ;
ENGEL, A .
PROTOPLASMA, 1988, 145 (2-3) :73-81
[2]   The band spectra of carbon monoxide [J].
Birge, RT .
PHYSICAL REVIEW, 1926, 28 (06) :1157-1181
[3]   ORIGIN OF TYROSYL CIRCULAR-DICHROISM OF TROPOMYOSIN [J].
BULLARD, B ;
MERCOLA, DA ;
MOMMAERTS, WFHM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 434 (01) :90-99
[4]   CONFORMATION AND ASSEMBLY CHARACTERISTICS OF TUBULIN AND MICROTUBULE PROTEIN FROM BOVINE BRAIN [J].
CLARK, DC ;
MARTIN, SR ;
BAYLEY, PM .
BIOCHEMISTRY, 1981, 20 (07) :1924-1932
[5]   A STUDY OF TUBULIN DIMER CONFORMATION BY NEAR-UV CIRCULAR-DICHROISM [J].
CLARK, DC ;
MARTIN, SR ;
BAYLEY, PM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1980, 97 (02) :628-634
[6]   A theory of intensity distribution in band systems [J].
Condon, E .
PHYSICAL REVIEW, 1926, 28 (06) :1182-1201
[7]   THE EFFECT OF CONFORMATION ON THE CD OF INTERACTING HELICES - A THEORETICAL-STUDY OF TROPOMYOSIN [J].
COOPER, TM ;
WOODY, RW .
BIOPOLYMERS, 1990, 30 (7-8) :657-676
[8]   THE PACKING OF ALPHA-HELICES - SIMPLE COILED-COILS [J].
CRICK, FHC .
ACTA CRYSTALLOGRAPHICA, 1953, 6 (8-9) :689-697
[9]   Elementary processes of photochemical reactions. [J].
Franck, J .
TRANSACTIONS OF THE FARADAY SOCIETY, 1926, 21 (03) :0536-0542
[10]   PROTEIN-CHEMICAL CHARACTERIZATION OF 3 STRUCTURALLY DISTINCT DOMAINS ALONG THE PROTOFILAMENT UNIT OF DESMIN 10-NM FILAMENTS [J].
GEISLER, N ;
KAUFMANN, E ;
WEBER, K .
CELL, 1982, 30 (01) :277-286