Folding and Domain Interactions of Three Orthologs of Hsp90 Studied by Single-Molecule Force Spectroscopy

被引:33
|
作者
Jahn, Markus [1 ]
Tych, Katarzyna [1 ]
Girstmair, Hannah [2 ]
Steinmassl, Maximilian [1 ]
Hugel, Thorsten [3 ]
Buchner, Johannes [2 ]
Rief, Matthias [1 ]
机构
[1] Tech Univ Munich, Phys Dept E22, D-85748 Garching, Bavaria, Germany
[2] Tech Univ Munich, Chem Dept, Chair Biotechnol, D-85748 Garching, Bavaria, Germany
[3] Univ Freiburg, Inst Phys Chem, D-79104 Freiburg, Baden Wurttembe, Germany
关键词
ENDOPLASMIC-RETICULUM HSP90; PEPTIDE-BINDING-ACTIVITY; N-TERMINAL DOMAIN; CHARGED LINKER; CONFORMATIONAL-CHANGES; CHAPERONE MACHINERY; CO-CHAPERONES; ATPASE CYCLE; GRP94; PROTEINS;
D O I
10.1016/j.str.2017.11.023
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 heat-shock protein 90 (Hsp90) molecular chaperones are highly conserved across species. However, their dynamic properties can vary significantly from organism to organism. Here we used high-precision optical tweezers to analyze the mechanical properties and folding of different Hsp90 orthologs, namely bacterial Hsp90 (HtpG) and Hsp90 from the endoplasmic reticulum (ER) (Grp94), as well as from the cytosol of the eukaryotic cell (Hsp82). We find that the folding rates of Hsp82 and HtpG are similar, while the folding of Grp94 is slowed down by misfolding of the N-terminal domain. Furthermore, the domain interactions mediated by the charged linker, involved in the conformational cycles of all three orthologs, are much stronger for Grp94 than for Hsp82, keeping the N-terminal domain and the middle domain in close proximity. Thus, the ER resident Hsp90 ortholog differs from the cytosolic counterparts in basic functionally relevant structural properties.
引用
收藏
页码:96 / +
页数:14
相关论文
共 50 条
  • [1] Folding and assembly of the large molecular machine Hsp90 studied in single-molecule experiments
    Jahn, Markus
    Buchner, Johannes
    Hugel, Thorsten
    Rief, Matthias
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (05) : 1232 - 1237
  • [2] Single-Molecule Force Spectroscopy of Protein Folding
    Petrosyan, Rafayel
    Narayan, Abhishek
    Woodside, Michael T.
    JOURNAL OF MOLECULAR BIOLOGY, 2021, 433 (20)
  • [3] A folding nucleus and minimal ATP binding domain of Hsp70 identified by single-molecule force spectroscopy
    Bauer, Daniela
    Meinhold, Sarah
    Jakob, Roman P.
    Stigler, Johannes
    Merkel, Ulrich
    Maier, Timm
    Rief, Matthias
    Zoldak, Gabriel
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (18) : 4666 - 4671
  • [4] A folding nucleus and minimal ATP binding domain of Hsp70 identified by single-molecule force spectroscopy
    Zoldak, G.
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2019, 48 : S178 - S178
  • [5] A folding nucleus and minimal ATP binding domain of Hsp70 identified by single-molecule force spectroscopy
    Zoldak, G.
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2019, 48 : S60 - S60
  • [6] Single-Molecule Force Spectroscopy of Membrane Protein Folding
    Wijesinghe, W. C. Bhashini
    Min, Duyoung
    JOURNAL OF MOLECULAR BIOLOGY, 2023, 435 (11)
  • [7] Reconstructing Folding Energy Landscapes by Single-Molecule Force Spectroscopy
    Woodside, Michael T.
    Block, Steven M.
    ANNUAL REVIEW OF BIOPHYSICS, VOL 43, 2014, 43 : 19 - 39
  • [8] Quantifying the Chain Folding in Polymer Single Crystals by Single-Molecule Force Spectroscopy
    Ma, Ziwen
    Yang, Peng
    Zhang, Xiaoye
    Jiang, Ke
    Song, Yu
    Zhang, Wenke
    ACS MACRO LETTERS, 2019, 8 (09) : 1194 - 1199
  • [9] The Interactions of Spore-Coat Morphogenetic Proteins Studied by Single-Molecule Recognition Force Spectroscopy
    Qiao, Haiyan
    Krajcikova, Daniela
    Liu, Caisheng
    Li, Yongjun
    Wang, Hongda
    Barak, Imrich
    Tang, Jilin
    CHEMISTRY-AN ASIAN JOURNAL, 2012, 7 (04) : 725 - 731
  • [10] Hsp90 structure and function studied by NMR spectroscopy
    Didenko, Tatiana
    Duarte, Afonso M. S.
    Karagoz, G. Elif
    Rudiger, Stefan G. D.
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2012, 1823 (03): : 636 - 647