Cornelis W. Hilbers

Lipid transfer proteins enhance cell wall extension in tobacco

Plant cells are enclosed by a rigid cell wall that counteracts the internal osmotic pressure of the vacuole and limits the rate and direction of cell enlargement. When developmental or physiological cues induce cell extension, plant cells increase wall plasticity by a process called loosening. It was demonstrated previously that a class of proteins known as expansins are mediators of wall loosening. Here, we report a type of cell wall–loosening protein that does not share any homology with expansins but is a member of the lipid transfer proteins (LTPs). LTPs are known to bind a large range of lipid molecules to their hydrophobic cavity, and we show here that this cavity is essential for the cell wall–loosening activity of LTP. Furthermore, we show that LTP-enhanced wall extension can be described by a logarithmic time function. We hypothesize that LTP associates with hydrophobic wall compounds, causing nonhydrolytic disruption of the cell wall and subsequently facilitating wall extension.

Floating stereospecific assignment revisited: Application to an 18 kDa protein and comparison with J-coupling data

We report a floating chirality procedure to treat nonstereospecifically assigned methylene orisopropyl groups in the calculation of protein structures from NMR data using restrainedmolecular dynamics and simulated annealing. The protocol makes use of two strategies toinduce the proper conformation of the prochiral centres: explicit atom ‘swapping’ followingan evaluation of the NOE energy term, and atom ‘floating’ by reducing the angle andimproper force constants that enforce a defined chirality at the prochiral centre. The individualcontributions of both approaches have been investigated. In addition, the effects of accuracyand precision of the interproton distance restraints were studied. The model system employedis the 18 kDa single-stranded DNA binding protein encoded by Pseudomonas bacteriophagePf3. Floating chirality was applied to all methylene and isopropyl groups that give rise to non-degenerate NMR signals, and the results for 34 of these groups were compared to J-couplingdata. We conclude that floating stereospecific assignment is a reliable tool in protein structurecalculation. Its use is beneficial because it allows the distance restraints to be extracteddirectly from the measured peak volumes without the need for averaging or addingpseudoatom corrections. As a result, the calculated structures are of a quality almostcomparable to that obtained with stereospecific assignments. As floating chirality furthermoreis the only approach treating prochiral centres that ensures a consistent assignment of the twoproton frequencies in a single structure, it seems to be preferable over using pseudoatoms or(R-6) averaging.

Solution structure of the pseudoknot of SRV-1 RNA, involved in ribosomal frameshifting

Abstract RNA pseudoknots play important roles in many biological processes. In the simian retrovirus type-1 (SRV-1) a pseudoknot together with a heptanucleotide slippery sequence are responsible for programmed ribosomal frameshifting, a translational recoding mechanism used to control expression of the Gag-Pol polyprotein from overlapping gag and pol open reading frames. Here we present the three-dimensional structure of the SRV-1 pseudoknot determined by NMR. The structure has a classical H-type fold and forms a triple helix by interactions between loop 2 and the minor groove of stem 1 involving base-base and base-sugar interactions and a ribose zipper motif, not identified in pseudoknots so far. Further stabilization is provided by a stack of five adenine bases and a uracil in loop 2, enforcing a cytidine to bulge. The two stems of the pseudoknot stack upon each other, demonstrating that a pseudoknot without an intercalated base at the junction can induce efficient frameshifting. Results of mutagenesis data are explained in context with the present three-dimensional structure. The two base-pairs at the junction of stem 1 and 2 have a helical twist of approximately 49°, allowing proper alignment and close approach of the three different strands at the junction. In addition to the overwound junction the structure is somewhat kinked between stem 1 and 2, assisting the single adenosine in spanning the major groove of stem 2. Geometrical models are presented that reveal the importance of the magnitude of the helical twist at the junction in determining the overall architecture of classical pseudoknots, in particular related to the opening of the minor groove of stem 1 and the orientation of stem 2, which determines the number of loop 1 nucleotides that span its major groove.

Essential spaces defined by NMR structure ensembles and molecular dynamics simulation show significant overlap

Large concerted motions of proteins which span its “essential space,” are an important component of protein dynamics. We investigate to what extent structure ensembles generated with standard structure calculation techniques such as simulated annealing can capture these motions by comparing them to long‐time molecular dynamics (MD) trajectories. The motions are analyzed by principal component analysis and compared using inner products of eigenvectors of the respective covariance matrices. Two very different systems are studied, the β‐spectrin PH domain and the single‐stranded DNA binding protein (ssDBP) from the filamentous phage Pf3. A comparison of the ensembles from NMR and MD shows significant overlap of the essential spaces, which in the case of ssDBP is extraordinarily high. The influence of variations in the specifications of distance restraints is investigated. We also study the influence of the selection criterion for the final structure ensemble on the definition of mobility. The results suggest a modified criterion that improves conformational sampling in terms of amplitudes of correlated motion. Proteins 31:370–382, 1998.

Tryptophan mediated photoreduction of disulfide bond causes unusual fluorescence behaviour of Fusarium solani pisi cutinase

The fluorescence signal of the single tryptophan residue (Trp69) of Fusarium solani pisi cutinase is highly quenched. However, prolonged irradiation of the enzyme in the tryptophan absorption band causes an increase of the tryptophan fluorescence quantum yield by an order of magnitude. By using a combination of NMR spectroscopy and chemical detection of free thiol groups with a sulfhydryl reagent we could unambiguously show that the unusual fluorescence behaviour of Trp69 in cutinase is caused by the breaking of the disulfide bond between Cys31 and Cys109 upon irradiation, while the amide‐aromatic hydrogen bond between Ala32 and Trp69 remains intact. This is the first example of tryptophan mediated photoreduction of a disulfide bond in proteins.

Improving the quality of protein structures derived by NMR spectroscopy

Biomolecular structures provide the basis for many studies in several research areas such as homology modelling, structure-based drug design and functional genomics. It is an important prerequisite that the structure is reliable in terms of accurate description of the experimental data, and in terms of good quality of local- and overall geometry. Recent surveys indicate that structures solved by NMR-spectroscopy normally are of lower precision than high-resolution X-ray structures. Here, we present a refinement protocol that improves the quality of protein structures determined by NMR-spectroscopy to the level of those determined by high resolution X-ray crystallography in terms of local geometry. The protocol was tested on experimental data of the proteins IL4 and Ubiquitin and on simulated data of the protein Crambin. In almost all aspects, the protocol yielded better results in terms of accuracy and precision. Independent validation of the results for Ubiquitin, using residual dipolar couplings, indicates that the ensemble of NMR structure is substantially improved by the protocol.

New developments in structure determination of pseudoknots

Recently, several high‐resolution structures of RNA pseudoknots have become available. Here we review the progress in this area. The majority of the structures obtained belong to the classical or H‐type pseudoknot family. The most complicated pseudoknot structure elucidated so far is the Hepatitis Delta Virus ribozyme, which forms a nested double pseudoknot. In particular, the structure–function relationships of the H‐type pseudoknots involved in translational frameshifting have received much attention. All molecules considered show interesting new structural motifs.

Heteronuclear scalar couplings in the bases and sugar rings of nucleic acids: Their determination and application in assignment and conformational analysis

The scalar coupling constants in uniformly isotope‐enriched [13C, 15N] nucleotide 5′‐monophosphates (5′‐NMPs) and in various non‐labelled cyclic nucleotides were investigated. These model compounds yielded an almost complete set of homonuclear and heteronuclear coupling constants in ribonucleotides, the knowledge of which is useful in designing novel heteronuclear NMR experiments and opens up new possibilities in the structure determination of larger nucleic acids. Three sets of heteronuclear coupling constants were obtained: (1) conformation‐independent 1H–13C, 1H–15N, 13C–15N, 13C–13C and 15N–15N coupling constants in the base, knowledge of which is essential in optimizing and designing new NMR experiments, which use the coherent transfer of magnetization via the J‐coupling network in the nucleic acid base and sugar; (2) 1H–13C coupling constants, 3JH1′C4/2 and 3JH1′C8/6, monitoring the glycosidic torsion angle χ, give important information on the rotamer distribution around the χ angle; a new parameterization of the Karplus equations is presented; and (3) conformation‐dependent one‐bond and multiple bond 1H–13C coupling constants in the ribose sugar. Conformationally rigid, cyclic, nucleotides were used to determine multiple bond 1H–13C coupling constants in pure N‐type and pure S‐type sugar rings. Equations were derived for the determination of the fraction S‐type sugar, pS, from the three‐bond JCH couplings 3JH3′C1′, 3JH2′C4′, 3JH1′C3′ and 3JH4′C2′. Their values for pure N‐ and S‐type sugar conformations were used to derive Karplus equations, which describe the dependence of these coupling constants on the phase angle, P.

The structure of the lantibiotic lacticin 481 produced by Lactococcus lactis : location of the thioether bridges

The lantibiotic lacticin 481 is a bacteriocin produced by Lactococcus lactis ssp. lactis. This polypeptide contains 27 amino acids, including the unusual residues dehydrobutyrine and the thioether‐bridging lanthionine and 3‐methyllanthionine. Lacticin 481 belongs to a structurally distinct group of lantibiotics, which also include streptococcin A‐FF22, salivaricin A and variacin. Here we report the first complete structure of this type of lantibiotic. The exact location of the thioether bridges in lacticin 481 was determined by a combination of peptide chemistry, mass spectrometry and NMR spectroscopy, showing connections between residues 9 and 14, 11 and 25, and 18 and 26.

Nuclear magnetic resonance studies on yeast tRNAPhe. III. Assignments of the iminoproton resonances of the tertiary structure by means of nuclear Overhauser effect experiments at 500 MHz

Resonances of the water exchangeable iminoprotons of the tertiary structure of yeast tRNAPhe were studied by experiments involving Nuclear Overhauser Effects (NOEs). Direct NOE evidence is presented for the assignment of all resonances of iminoprotons participating in tertiary basepairing (except that of G19C56 which was assigned by an elimination procedure). The present results in conjunction with our previous assignment of secondary iminoprotons constitute for the first time a complete spectral assignment of all iminoprotons participating in basepairing in yeast tRNAPhe. In addition we have been able to assign the non(internally) hydrogen bonded N1 proton of psi 55 as well as the N3 proton of this residue, which is one of the two iminoprotons hydrogen bonded to a phosphate group according to X-ray results. No evidence could be obtained for the existence in solution of the other iminoproton-phosphate interaction: that between U33 N3H and P36 located in the anticodon loop. Remarkable is the assignment of a resonance at 12.4 - 12.5 ppm to the iminoproton of the tertiary basepair T54m1A58. The resonance positions obtained for the iminoprotons of G18 (9.8 ppm) and m2(2)G26 (10.4 ppm) are surprisingly far upfield considering that these protons are involved in hydrogen bonds according to X-ray diffraction results. As far as reported by changes in chemical shifts of iminoproton resonances the main structural event induced by Mg++ ions takes place near the tertiary interactions U8A14 and G22m7G46.