Karol Maskos

Probing the interface in a human co-chaperonin heptamer: residues disrupting oligomeric unfolded state identified.

BackgroundThe co-chaperonin protein 10 (cpn10) assists cpn60 in the folding of nonnative polypeptides in a wide range of organisms. All known cpn10 molecules are heptamers of seven identical subunits that are linked together by β-strand interactions at a large and flexible interface. Unfolding of human mitochondrial cpn10 in urea results in an unfolded heptameric state whereas GuHCl additions result in unfolded monomers. To address the role of specific interface residues in the assembly of cpn10 we prepared two point-mutated variants, in each case removing a hydrophobic residue positioned at the subunit-subunit interface.ResultsReplacing valine-100 with a glycine (Val100Gly cpn10) results in a wild-type-like protein with seven-fold symmetry although the thermodynamic stability is decreased and the unfolding processes in urea and GuHCl both result in unfolded monomers. In sharp contrast, replacing phenylalanine-8 with a glycine (Phe8Gly cpn10) results in a protein that has lost the ability to assemble. Instead, this protein exists mostly as unfolded monomers.ConclusionsWe conclude that valine-100 is a residue important to adopt an oligomeric unfolded state but it does not affect the ability to assemble in the folded state. In contrast, phenylalanine-8 is required for both heptamer assembly and monomer folding and therefore this mutation results in unfolded monomers at physiological conditions. Despite the plasticity and large size of the cpn10 interface, our observations show that isolated interface residues can be crucial for both the retention of a heptameric unfolded structure and for subunit folding.

Identification of the bright-greenish-yellow-fluorescence (BGY-F) compound on cotton lint associated with aflatoxin contamination in cottonseed

In order to characterize the structure of the bright-greenish-yellow-fluorescence (BGY-F) compound on cotton lint associated with aflatoxin contamination in cotton seed, various in vitro and in vivo natural BGY-F reaction products were prepared. Under similar high pressure liquid chromatography separation with variable wavelength and programmable fluorescence detection (HPLC-UV/FL), combined with atmospheric pressure ionization and mass spectral determinations it was found that the BGY-F reaction products prepared from three preparations: (a) kojic acid (KA) + peroxidase (soybean peroxide or horseradish type VI and type II) + H2O2, or (b) detached fresh cotton locules + KA + H2O2, or (c) attached field cotton locules that were treated with a spore suspension of aflatoxigenic Aspergillus flavus, all resulted in identical chromatographic characteristics, and all exhibited a molecular weight of 282. Further characterization of the BGY-F reaction product with 1H- and 13C-NMR spectroscopic analysis revealed that it was a dehydrogenator dimer of 2 KA, linked through the C-6 positions.

The physical and NMR characterizations of allyl‐ and crotylcelluloses

Tri-O-allylcellulose (degree of polymerization, DP ∼112) was prepared in ∼91% yield, and tri-O-crotylcellulose (DP ∼138) was prepared in ∼56% yield from microcrystalline cellulose (DP ∼172, and polydispersity index, PDI ∼1.95) using modified literature methods. Number-average molecular weight (Mn = 31,600), weight-average molecular weight (Mw = 191,800), and PDI = 6.07 data suggested that tri-O-allylcellulose may be crosslinking in air to generate branched chains. The polymer was stabilized with 100 ppm butylated hydroxy toluene (BHT). The material without BHT experienced glass transition (Tg, differential-scanning calorimetry, DSC) between −2 and +3 °C, crosslinked beyond 100 °C, and degraded at 298.6 °C (by thermogravimetric analysis, TGA). Mn (45,100), Mw (118,200), PDI (2.62), and thermal data (Tg − 5 to +3 °C, melting point 185.8 °C, recrystallization 168.9 °C, and degradation 343.6 °C) on tri-O-crotylcellulose suggested that the polymer was formed with about the same polydispersity as the starting material and is heat stable. While allylcellulose generated continuous flexible yellow films by solution casting, crotylcellulose precipitated from solution as brittle white flakes. Dynamic mechanical analysis (DMA) data on allylcellulose films (Tg − 29.1 °C, Youngs modulus 5.81 × 108 Pa) suggest that the material is tough and flexible at room temperature. All 1H and 13C resonances in the NMR spectra were identified and assigned using the following methods: Double-quantum filter correlation spectroscopy (DQF COSY) was used to assign the network of seven protons in the anhydroglucose portion of the repeat unit. The proton assignments were verified and confirmed by total correlation spectroscopy (TOCSY). A combination of heteronuclear single-quantum coherence (HSQC) and 13C spectroscopies were used to identify all bonded carbon–hydrogen pairs in the anhydroglucose portion of the repeat unit, and assign the carbon nuclei chemical shift values. Heteronuclear multiple bond correlation (HMBC) spectroscopy was used to connect the resonances of methines and methylenes at positions 2, 3, and 6 to the methylene resonances of the allyl ethers. TOCSY was used again to identify the fifteen 1H resonances in the three pendant allyl groups. Finally, a combination of HSQC, HMBC, and 13C spectroscopies were used to identify each carbon in the allyl pendants at 2, 3, and 6. Because of line broadening and signal overlap, we were unable to identify the conformational arrangement about the C5 and C6 bond in tri-O-allyl- and tri-O-crotylcelluloses.

Characterization of tri-o-methylcellulose by one- and two-dimensional NMR methods†

Tri-O-methylcellulose was prepared from partially O-methylated cellulose and its chemical shifts ( 1 H and 13 C), and proton coupling constants were assigned using the following NMR methods: (1) One-dimensional 1 H and 13 C spectra of the title compound were used to assign functional groups and to compare with literature data; (2) double quantum filtered proton-proton correlation spectroscopy ( 1 H, 1 H DQF-COSY) was used to assign the chemical shifts of the network of 7 protons in the anhydroglucose portion of the repeat unit; (3) the heteronuclear single-quantum coherence (HSQC) spectrum was used to establish connectivities between the bonded protons and carbons; (4) the heteronuclear multiple-bond correlation (HMBC) spectrum was used to connect the hydrogens of the methyl ethers to their respective sugar carbons; (5) the combination of HSQC and HMBC spectra was used to assign the 13 C shifts of the methyl ethers; (6) all spectra were used in combination to verify the assigned chemical shifts; (7) first-order proton coupling constants data (J H,H in Hz) were obtained from the resolution-enhanced proton spectra. The NMR spectra of tri-O-methylcellulose and other cellulose ethers do not resemble the spectra of similarly substituted cellobioses. Although the 1 H and 13 C shifts and coupling constants of 2,3,6-tri-O-methylcellulose closely resemble those of methyl tetra-O-methyl-β-D-glucoside, there are differences with regard to the chemical shifts and the order of appearances of the resonating nuclei of the methyl ether appendages and the proton at position 4 in the pyranose ring. H4 in tri-O-methylcellulose is deshielded by the acetal system comprising the β-1→4 linkage, and it resonates downfield. H4 in the permethylated glucoside is not as deshielded by the equitorial O-methyl group at C4, and it resonates upfield. The order of appearance of the 1 H and 13 C resonances in the spectra of the tri-O-methylcellulose repeat unit (from upfield to downfield) are H2 < H3 < H5 < H6a < H3a < H2a < pro R H6B < H4 < pro S H6A « H1 and C6a < C3a < C2a < C6 < C5 < C4 < C2 < C3 « C1, respectively. Close examination of the pyranose ring coupling constants of the repeat unit in tri-O-methylcellulose supports the 4 C 1 arrangement of the glucopyranose ring. Examination of the proton coupling constants about the C5-C6 bond (J 5,6A and J 5,6B ) in the nuclear Overhauser effect difference spectra revealed that the C6 O-methyl group is predominantly in the gauche gauche conformation about the C5-C6 bond for the polymer in solution.

Selective conversion of O-succinimidyl carbamates to N-(O-carbamoyl)-succinmonoamides and ureas

N-Monoalkyl-O-succinimidyl carbamates reacted with primary and secondary amines to produce ureas. However, N,N-dialkyl-O-succinimidyl carbamates reacted with primary and secondary amines, via succinimide ring opening, to afford N-(O-carbamoyl)-succinmonoamide derivatives. This ring-opening trend was also true with hydroxy and alkoxy nucleophiles. Herein, general methods for the synthesis and NMR characterization of N-(O-carbamoyl)-succinmonoamides are reported.