A Rubber-Like Protein in Insect Cuticle

1960 ◽  
Vol 37 (4) ◽  
pp. 889-907 ◽  
Author(s):  
TORKEL WEIS-FOGH

1. A new type of hyaline, colourless cuticle, called rubber-like cuticle, is described and analysed qualitatively with respect to mechanical behaviour, structure and composition. Externally it is covered by ordinary thin epicuticle, but otherwise it represents the simplest type of cuticle known and consists only of thin continuous lamellae of chitin (0-2 µ) separated and glued together by an elastic protein, resilin, not hitherto described. There are only traces of water-soluble substances present and resilin sometimes occurs as pure, hyaline patches more than 100 µ thick and suitable for macroscopic experiments. 2. In all physical respects, resilin behaves like a swollen isotropic rubber but the rigid experimental proof is given elsewhere (Weis-Fogh, 1961). An outstanding feature is the complete lack of flow not paralleled by other natural or synthetic rubbers. 3. Resilin resembles elastin but it is devoid of colour and has a different and characteristic amino-acid composition (Bailey & Weis-Fogh, 1961). The nature of the cross-linkages is unknown at present but they are extremely stable, of a co-valent type and different from other known cross-linkages in proteins. This accounts for its insolubility and resistance to all agents which do not break the peptide backbone. 4. Resilin is a structure protein in which the primary chains show little or no tendency to form secondary structures; they are bound together in a uniform three-dimensional network (the tertiary structure) with no potential limits as to size.

2013 ◽  
Vol 69 (2) ◽  
pp. o172-o173 ◽  
Author(s):  
Irene Nehls ◽  
Olaf Hanebeck ◽  
Roland Becker ◽  
Franziska Emmerling

The title compound, {2-[(2-carbamoylethyl)amino]-3-methylpentanoic acid}, C9H18N2O3, is of interest with respect to its biological activity. It was formed during an addition reaction between acrylamide and the amino acid isoleucine. The crystal structure is a three-dimensional network built up by intermolecular N—H...O and O—H...N hydrogen bonds.


2004 ◽  
Vol 186 (21) ◽  
pp. 7420-7428 ◽  
Author(s):  
Beronda L. Montgomery ◽  
Elena Silva Casey ◽  
Arthur R. Grossman ◽  
David M. Kehoe

ABSTRACT All known phycobiliproteins have light-harvesting roles during photosynthesis and are found in water-soluble phycobilisomes, the light-harvesting complexes of cyanobacteria, cyanelles, and red algae. Phycobiliproteins are chromophore-bearing proteins that exist as heterodimers of α and β subunits, possess a number of highly conserved amino acid residues important for dimerization and chromophore binding, and are invariably 160 to 180 amino acids long. A new and unusual group of proteins that is most closely related to the allophycocyanin members of the phycobiliprotein superfamily has been identified. Each of these proteins, which have been named allophycocyanin-like (Apl) proteins, apparently contains a 28-amino-acid extension at its amino terminus relative to allophycocyanins. Apl family members possess the residues critical for chromophore interactions, but substitutions are present at positions implicated in maintaining the proper α-β subunit interactions and tertiary structure of phycobiliproteins, suggesting that Apl proteins are able to bind chromophores but fail to adopt typical allophycocyanin conformations. AplA isolated from the cyanobacterium Fremyella diplosiphon contained a covalently attached chromophore and, although present in the cell under a number of conditions, was not detected in phycobilisomes. Thus, Apl proteins are a new class of photoreceptors with a different cellular location and structure than any previously described members of the phycobiliprotein superfamily.


IUCrData ◽  
2017 ◽  
Vol 2 (7) ◽  
Author(s):  
Ana Karen Giron-Moreno ◽  
Nancy Lara-Sánchez ◽  
Gabriela Moreno-Martínez ◽  
Cándida Pastor-Ramírez ◽  
Eduardo Sánchez-Lara ◽  
...  

The heterometallic coordination compound [Cu(Lys)(phen)]2V4O12·4H2O (Lys is the amino acid lysine, C6H14N2O2, and phen is 1,10-phenanthroline, C12H8N2) lies across an inversion centre. Two [Cu(Lys)(phen)]2+ units coordinate to the cyclo-vanadate fragment and the formula unit is completed by four solvent water molecules. The lysine ligand is in the zwitterionic form and chelates the CuII atom via the α-NH2 and α-COO− donor groups, while the ∊-NH3 + group is involved in intramolecular hydrogen bonds with the central [V4O12]4− core and with solvent water molecules. In the crystal, N—H...O and O—H...O hydrogen bonds connect the components of the structure to form a three-dimensional network. The crystal structure is further stabilized by π–π interactions involving the phen ligands. The lysine group is disordered over two sets of sites with refined occupancies of 0.534 (11) and 0.466 (11).


1988 ◽  
Vol 53 (11) ◽  
pp. 2549-2573 ◽  
Author(s):  
Victor J. Hruby ◽  
Wayne L. Cody ◽  
Ana Maria de Lauro Castrucci ◽  
Mac E. Hadley

Conformational and biological analysis of the linear 4-11 fragment analogues, Ac-[Nle4]-α-MSH4-11-NH2 (II) and Ac-[Nle4, D-Phe7]-α-MSH4-11-NH2 (III) and related analogues have been undertaken. In solution, the peptide backbone is flexible, but in the case of D-Phe7 analogues an interaction of the His6, D-Phe7 and Arg8 amino acid side chain groups may be present based on the shielding patterns observed in the proton NMR and on comparison of NT1 values. The importance of the position 7 to the biological and conformational properties was further examined by substitution of either L- or D-phenylglycine (Pgl) or L- and D-1,2,3,4-tetrahydroisoquinoline carboxylic acid (Tic) for phenylalanine-7. Ac-[Nle4, Pgl7]-α-MSH4-11-NH2 (IV), Ac-[Nle4, D-Pgl7]-α-MSH4-11-NH2 (V), Ac-[Nle4, Tic7]-α-MSH4-11-NH2 (VI), and Ac-[Nle4, D-Tic7]-α-MSH4-11-NH2 (VII) were prepared. These substituted analogues were examined for their biological activities and conformational properties with emphasis on the three-dimensional orientation of the aromatic ring in the position 7, and the effects of the aromatic ring on adjacent amino acids, and on biological activities. The relative potencies of the analogues in the frog skin assay system were: II (1·00); III (118); IV (82·4); V (0·18); VI (0·18); and VII (0·14); and in the lizard skin bioassay they were: II (1·00); III (10·0); IV (0·14); V (0·005); VI (0·00025); and VII (0·01). On the basis of the NMR studies the L-phenylglycine substitution results in an enhanced ring stacking interaction between the phenyl ring of Pgl7 and the indole ring of Trp9. The 1,2,3,4-tetrahydroisoquinoline carboxylic acid (Tic) substitution leads to significant backbone restriction and an interaction of the alpha proton of His6 with the carbonyl of Glu5. The possible relationships of these effects to biological activity are discussed.


1979 ◽  
Vol 34 (9) ◽  
pp. 1234-1236 ◽  
Author(s):  
Axel Czybulka ◽  
Hans-Uwe Schuster

Abstract The ternary compound Li3Ce5Ge4 has been prepared and structurally characterized. It crystallizes orthorhombically (a = 1885 pm, b = 694.7 pm, c = 447.6 pm, space group B 2 mm). The structure shows germanium chains in a three-dimensional network of metal atoms.


Functional studies on interferon would be helped by a three-dimensional structure for the molecule. However, it may be several years before the structure of the protein is determined by X-ray crystallography. We have therefore used available methods for predicting the secondary - and the tertiary - structure of a protein from its amino acid sequence to propose a tertiary model involving the packing of four a-helices. Details of this work have been published elsewhere (Sternberg & Cohen 1982).


2015 ◽  
Vol 71 (3) ◽  
pp. 185-187 ◽  
Author(s):  
Annaliese E. Thuijs ◽  
George Christou ◽  
Khalil A. Abboud

The title dodecanuclear Mn complex, namely dodeca-μ2-acetato-κ24O:O′-tetraaquatetra-μ2-nitrato-κ8O:O′-tetra-μ4-oxido-octa-μ3-oxido-tetramanganese(IV)octamanganese(III) nitromethane tetrasolvate, [Mn12(CH3COO)12(NO3)4O12(H2O)4]·4CH3NO2, was synthesized by the reaction of Mn2+and Ce4+sources in nitromethane with an excess of acetic acid. This compound is distinct from the previously known single-molecule magnet [Mn12O12(O2CMe)16(H2O)4], synthesized by Lis [Acta Cryst.(1980), B36, 2042–2044]. It is the first Mn12-type molecule containing nitrate ligands to be directly synthesized without the use of a preformed cluster. Additionally, this molecule is distinct from all other known Mn12complexes due to intermolecular hydrogen bonds between the nitrate and water ligands, which give rise to a three-dimensional network. The complex is compared to other known Mn12molecules in terms of its structural parameters and symmetry.


2017 ◽  
Vol 15 (03) ◽  
pp. 1750009 ◽  
Author(s):  
Bruno Grisci ◽  
Márcio Dorn

The development of computational methods to accurately model three-dimensional protein structures from sequences of amino acid residues is becoming increasingly important to the structural biology field. This paper addresses the challenge of predicting the tertiary structure of a given amino acid sequence, which has been reported to belong to the NP-Complete class of problems. We present a new method, namely NEAT–FLEX, based on NeuroEvolution of Augmenting Topologies (NEAT) to extract structural features from (ABS) proteins that are determined experimentally. The proposed method manipulates structural information from the Protein Data Bank (PDB) and predicts the conformational flexibility (FLEX) of residues of a target amino acid sequence. This information may be used in three-dimensional structure prediction approaches as a way to reduce the conformational search space. The proposed method was tested with 24 different amino acid sequences. Evolving neural networks were compared against a traditional error back-propagation algorithm; results show that the proposed method is a powerful way to extract and represent structural information from protein molecules that are determined experimentally.


2020 ◽  
Vol 20 (4) ◽  
pp. 175-205
Author(s):  
Aigul S. Istomina ◽  
◽  
Olga V. Bushkova ◽  

The second part of the review describes the prospects of using alternative polymer binders for composite electrodes of lithium electrochemical systems. Possible options having been taken into account, the most popular commercially-available synthetic polymers with functional group (the ones forming aqueous solutions or dispersions predominantly) and water-soluble polymers of natural origin are considered. The versatility of such materials is their distinctive feature. The availability of salt forms for natural and synthetic polymers, many of which are polyelectrolytes, makes it possible to significantly affect the ion transfer in the composite electrode mass, reducing the polarization of the electrodes and improving the power characteristics of batteries. The ability to form “artificial SEI” and / or form a three-dimensional network with self-healing cross-links between macromolecules allows long-term safe cycling, the latter being especially important for active materials with very large volume changes during lithium intercalation / deintercalation (e.g. silicon).


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