Insight into self-assembly of malonate-based copper(II) phenanthroline complexes: Syntheses, crystal structures and properties

Polyhedron ◽  
2014 ◽  
Vol 68 ◽  
pp. 324-333 ◽  
Author(s):  
Yue-Qing Zheng ◽  
Xiang-Sheng Zhai ◽  
Ling Jin ◽  
Hong-Lin Zhu ◽  
Jian-Li Lin ◽  
...  
IUCrJ ◽  
2018 ◽  
Vol 5 (6) ◽  
pp. 765-779 ◽  
Author(s):  
Patricia Casino ◽  
Roberto Gozalbo-Rovira ◽  
Jesús Rodríguez-Díaz ◽  
Sreedatta Banerjee ◽  
Ariel Boutaud ◽  
...  

Basement membranes are extracellular structures of epithelia and endothelia that have collagen IV scaffolds of triple α-chain helical protomers that associate end-to-end, forming networks. The molecular mechanisms by which the noncollagenous C-terminal domains of α-chains direct the selection and assembly of the α1α2α1 and α3α4α5 hetero-oligomers found in vivo remain obscure. Autoantibodies against the noncollagenous domains of the α3α4α5 hexamer or mutations therein cause Goodpasture's or Alport's syndromes, respectively. To gain further insight into oligomer-assembly mechanisms as well as into Goodpasture's and Alport's syndromes, crystal structures of noncollagenous domains produced by recombinant methods were determined. The spontaneous formation of canonical homohexamers (dimers of trimers) of these domains of the α1, α3 and α5 chains was shown and the components of the Goodpasture's disease epitopes were viewed. Crystal structures of the α2 and α4 noncollagenous domains generated by recombinant methods were also determined. These domains spontaneously form homo-oligomers that deviate from the canonical architectures since they have a higher number of subunits (dimers of tetramers and of hexamers, respectively). Six flexible structural motifs largely explain the architectural variations. These findings provide insight into noncollagenous domain folding, while supporting the in vivo operation of extrinsic mechanisms for restricting the self-assembly of noncollagenous domains. Intriguingly, Alport's syndrome missense mutations concentrate within the core that nucleates the folding of the noncollagenous domain, suggesting that this syndrome, when owing to missense changes, is a folding disorder that is potentially amenable to pharmacochaperone therapy.


2009 ◽  
Vol 113 (13) ◽  
pp. 3088-3095 ◽  
Author(s):  
B. B. Koleva ◽  
T. Kolev ◽  
R. W. Seidel ◽  
M. Spiteller ◽  
H. Mayer-Figge ◽  
...  

Polyhedron ◽  
2006 ◽  
Vol 25 (15) ◽  
pp. 2967-2975 ◽  
Author(s):  
Stefania Tanase ◽  
Martin van Son ◽  
Gerard A. van Albada ◽  
René de Gelder ◽  
Elisabeth Bouwman ◽  
...  

2012 ◽  
Vol 41 (9) ◽  
pp. 2639 ◽  
Author(s):  
Yi-Xia Ren ◽  
Shan-Shan Xiao ◽  
Xiang-Jun Zheng ◽  
Li-Cun Li ◽  
Lin-Pei Jin

RSC Advances ◽  
2015 ◽  
Vol 5 (37) ◽  
pp. 29362-29369 ◽  
Author(s):  
Gaoshan Yang ◽  
Huiliang Wen ◽  
Chongbo Liu ◽  
Julianne Robbins ◽  
Yunhan Wen ◽  
...  

Three new inorganic–organic frameworks based on 3,4,5-tris(carboxymethoxy)benzoic acid and polynuclear metal-hydroxyl clusters were assembled. Photoluminescent and magnetic properties are investigated.


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