165 related articles for article (PubMed ID: 28528950)
1. Effects of cataract-causing mutations W59C and W151C on βB2-crystallin structure, stability and folding.
Zhao WJ; Xu J; Chen XJ; Liu HH; Yao K; Yan YB
Int J Biol Macromol; 2017 Oct; 103():764-770. PubMed ID: 28528950
[TBL] [Abstract][Full Text] [Related]
2. Introduction of an extra tryptophan fluorophore by cataract-associating mutations destabilizes βB2-crystallin and promotes aggregation.
Xu J; Zhao WJ; Chen XJ; Yao K; Yan YB
Biochem Biophys Res Commun; 2018 Oct; 504(4):851-856. PubMed ID: 30219234
[TBL] [Abstract][Full Text] [Related]
3. The importance of the last strand at the C-terminus in βB2-crystallin stability and assembly.
Zhang K; Zhao WJ; Leng XY; Wang S; Yao K; Yan YB
Biochim Biophys Acta; 2014 Jan; 1842(1):44-55. PubMed ID: 24120835
[TBL] [Abstract][Full Text] [Related]
4. A missense mutation in CRYBB2 leads to progressive congenital membranous cataract by impacting the solubility and function of βB2-crystallin.
Chen W; Chen X; Hu Z; Lin H; Zhou F; Luo L; Zhang X; Zhong X; Yang Y; Wu C; Lin Z; Ye S; Liu Y;
PLoS One; 2013; 8(11):e81290. PubMed ID: 24312286
[TBL] [Abstract][Full Text] [Related]
5. Association of partially folded lens betaB2-crystallins with the alpha-crystallin molecular chaperone.
Evans P; Slingsby C; Wallace BA
Biochem J; 2008 Feb; 409(3):691-9. PubMed ID: 17937660
[TBL] [Abstract][Full Text] [Related]
6. Cataract-linked mutation R188H promotes βB2-crystallin aggregation and fibrillization during acid denaturation.
Xi YB; Zhang K; Dai AB; Ji SR; Yao K; Yan YB
Biochem Biophys Res Commun; 2014 May; 447(2):244-9. PubMed ID: 24704203
[TBL] [Abstract][Full Text] [Related]
7. Cataract-causing mutation S228P promotes βB1-crystallin aggregation and degradation by separating two interacting loops in C-terminal domain.
Qi LB; Hu LD; Liu H; Li HY; Leng XY; Yan YB
Protein Cell; 2016 Jul; 7(7):501-15. PubMed ID: 27318838
[TBL] [Abstract][Full Text] [Related]
8. Congenital microcornea-cataract syndrome-causing mutation X253R increases βB1-crystallin hydrophobicity to promote aggregate formation.
Leng XY; Li HY; Wang J; Qi LB; Xi YB; Yan YB
Biochem J; 2016 Jul; 473(14):2087-96. PubMed ID: 27208166
[TBL] [Abstract][Full Text] [Related]
9. The congenital cataract-linked A2V mutation impairs tetramer formation and promotes aggregation of βB2-crystallin.
Xu J; Wang S; Zhao WJ; Xi YB; Yan YB; Yao K
PLoS One; 2012; 7(12):e51200. PubMed ID: 23236454
[TBL] [Abstract][Full Text] [Related]
10. Characterization of βB2-crystallin tryptophan mutants reveals two different folding states in solution.
Sun J; Morishima K; Inoue R; Sugiyama M; Takata T
Protein Sci; 2024 Jul; 33(7):e5092. PubMed ID: 38924206
[TBL] [Abstract][Full Text] [Related]
11. Creation of a new eye lens crystallin (Gambeta) through structure-guided mutagenic grafting of the surface of betaB2 crystallin onto the hydrophobic core of gammaB crystallin.
Kapoor D; Singh B; Subramanian K; Guptasarma P
FEBS J; 2009 Jun; 276(12):3341-53. PubMed ID: 19438717
[TBL] [Abstract][Full Text] [Related]
12. Unfolding of human lens recombinant betaB2- and gammaC-crystallins.
Fu L; Liang JJ
J Struct Biol; 2002 Sep; 139(3):191-8. PubMed ID: 12457849
[TBL] [Abstract][Full Text] [Related]
13. Congenital cataract-causing mutation βB1-L116P is prone to amyloid fibrils aggregation and protease degradation with low structural stability.
Liu J; Xu W; Wang K; Chen F; Ren L; Xu J; Yao K; Chen X
Int J Biol Macromol; 2022 Jan; 195():475-482. PubMed ID: 34896472
[TBL] [Abstract][Full Text] [Related]
14. BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons.
Dulle JE; Rübsam A; Garnai SJ; Pawar HS; Fort PE
Exp Eye Res; 2017 Feb; 155():85-90. PubMed ID: 28131617
[TBL] [Abstract][Full Text] [Related]
15. The cataract-related S39C variant increases γS-crystallin sensitivity to environmental stress by destroying the intermolecular disulfide cross-links.
Yang X; Xu J; Fu C; Jia Z; Yao K; Chen X
Biochem Biophys Res Commun; 2020 May; 526(2):459-465. PubMed ID: 32234236
[TBL] [Abstract][Full Text] [Related]
16. The cataract-causing mutation G75V promotes γS-crystallin aggregation by modifying and destabilizing the native structure.
Zhu S; Xi XB; Duan TL; Zhai Y; Li J; Yan YB; Yao K
Int J Biol Macromol; 2018 Oct; 117():807-814. PubMed ID: 29857103
[TBL] [Abstract][Full Text] [Related]
17. Deamidation in human lens betaB2-crystallin destabilizes the dimer.
Lampi KJ; Amyx KK; Ahmann P; Steel EA
Biochemistry; 2006 Mar; 45(10):3146-53. PubMed ID: 16519509
[TBL] [Abstract][Full Text] [Related]
18. Cataract-causing G91del mutant destabilised βA3 heteromers formation linking with structural stability and cellular viability.
Wang H; Tian Q; Xu J; Xu W; Yao K; Chen X
Br J Ophthalmol; 2022 Oct; 106(10):1473-1478. PubMed ID: 34489339
[TBL] [Abstract][Full Text] [Related]
19. Simultaneous stereoinversion and isomerization at the Asp-4 residue in βB2-crystallin from the aged human eye lenses.
Fujii N; Kawaguchi T; Sasaki H; Fujii N
Biochemistry; 2011 Oct; 50(40):8628-35. PubMed ID: 21877723
[TBL] [Abstract][Full Text] [Related]
20. Insight into Pathogenic Mechanism Underlying the Hereditary Cataract Caused by βB2-G149V Mutation.
Wu J; Chen S; Xu J; Xu W; Zheng S; Tian Q; Luo C; Chen X; Shentu X
Biomolecules; 2023 May; 13(5):. PubMed ID: 37238733
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
