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Solution structure of a de novo helical protein by 2D-NMR spectroscopy.

The de novo design of proteins represents a critical test for our knowledge of protein structure. However, no structure of a successfully designed protein has yet been reported. This paper reports the design and the tertiary structure of a de novo 35-residue helix-loop-helix protein (ALIN), with helices arranged in an anti-parallel manner. For the helical region, we designed sequences that have high helicities even as isolated peptides. A flexible loop containing glycine residues was used to connect the two helices and the interhelical hydrophobic interaction was stabilized by the introduction of an SS-bridge. This arrangement of two consecutive helices bridged by a disulfide bond is not observed in any natural proteins. The protein is highly soluble and monomeric in aqueous solution. The structure of ALIN, determined by 1H-NMR and distance geometry calculation, agrees well with the design. In addition, the exchange rates of amide protons indicate the presence of stable hydrogen bonds in the helical region. ALIN is the first de novo designed protein with a stable tertiary fold confirmed by NMR.

Amino Acid Sequence↗

Enzyme-substrate interactions. Structure of human carbonic anhydrase I complexed with bicarbonate.

The structure of HCAI-HCO3- complex has been refined with 10-1.6A X-ray diffraction data to an R-value of 17.7%. The structure reveals monodentate binding of the HCO3- anion at an apical tetrahedral position to the zinc ion. The binding mode and interactions of HCO3- in HCAI differ from that in HCAII. The activity linked H2O/OH- group in the free HCAI is replaced by the hydroxyl group of the bicarbonate anion. This result rules out the rearrangement of the bound HCO3- advocated earlier to explain the microscopic reversibility of the catalysed reaction. From the geometry of the H-bonds between Glu106-Thr199 pair and Glu117-His119 couple, the glutamic acids are expected to be ionized and accept H-bonds from their partners. The product-inhibiton by HCO3- anion is explained on the basis of proton localization on His119 in the Glu117-His119 couple. These results are consistent with the hypothesis that Glu117-His119 tunes the ionicity of the Zn2+ and the binding strength of HCO3- anion. A pi hydrogen bond is observed between a water and phenyl ring of the Tyr114 residue.

Bicarbonates↗

Crystal structure of a pyrimidine dimer-specific excision repair enzyme from bacteriophage T4: refinement at 1.45 A and X-ray analysis of the three active site mutants.

Crystallographic study of bacteriophage T4 endonuclease V, which is involved in the initial step of the pyrimidine dimer-specific excision repair pathway, has been carried out with respect to the wild-type and three different mutant enzymes. This enzyme catalyzes the cleavage of the N-glycosyl bond at the 5'-side of the pyrimidine dimer, and subsequently incises the phosphodiester bond at the apyrimidinic site through a beta-elimination reaction. The structure of the wild-type enzyme refined at 1.45 A resolution reveals the detailed molecular architecture. The enzyme is composed of a single compact domain classified as an all-alpha structure. The molecule is stabilized mainly by three hydrophobic cores, two of which include many aromatic side-chain interactions. The structure has a unique folding motif, where the amino-terminal segment penetrates between two major alpha-helices and prevents their direct contact, and it is incompatible with the close-packing category of helices for protein folding. The concave surface, covered with many positive charges, implies an interface for DNA binding. The glycosylase catalytic center, which comprises Glu23 and the surrounding basic residues Arg3, Arg22 and Arg26, lie in this basic surface. The crystal structures of the three active-site mutants, in which Glu23 was replaced by Gln(E23Q) and Asp (E23D), respectively, and Arg3 by Gln (R3Q), have been determined at atomic resolution. The backbone structures of the E23Q and R3Q mutants were almost identical with that of the wild-type, while the E23D mutation induces a small, but significant, change in the backbone structure, such as an increase of the central kink of the H1 helix at Pro25. In the catalytic center of the glycosylase, however, these three mutations do not generate notable movements of protein atoms, except for significant shifts of some bound water molecules. Thus, the structural differences between the wild-type and each mutant are confined to the remarkably small region around their replaced chemical groups. Combined with the biochemical studies and the difference circular dichroism measurements, these results allow us to conclude that the negatively charged carboxyl group of Glu23 is essential for the cleavage of the N-glycosyl bond, and that the positively charged guanidino group of Arg3 is crucial to bind the substrate, a DNA duplex containing a pyrimidine dimer. The amino terminal alpha-amino group is located at a position approximately 4.4 A away from the carboxyl group of Glu23. These structural features are generally consistent with the reaction scheme proposed by Dodson and co-workers.

Amino Acid Sequence↗

Crystallisation of RNA-protein complexes. II. The application of protein engineering for crystallisation of the U1A protein-RNA complex.

The hairpin is one of the most commonly found structural motifs of RNA and is often a binding site for proteins. Crystallisation of U1A spliceosomal protein bound to a RNA hairpin, its natural binding site on U1snRNA, is described. RNA oligonucleotides were synthesised either chemically or by in vitro transcription using T7 RNA polymerase and purified to homogeneity by gel electrophoresis. Crystallisation trials with the wild-type protein sequence and RNA hairpins containing various stem sequences and overhanging nucleotides only resulted in a cubic crystal form which diffracted to 7-8 A resolution. A new crystal form was grown by using a protein variant containing mutations of two surface residues. The N-terminal sequence of the protein was also varied to reduce heterogeneity which was detected by protein mass spectrometry. A further crystallisation search using the double mutant protein and varying the RNA hairpins resulted in crystals diffracting to beyond 1.7 A. The methods and strategy described in this paper may be applicable to crystallisation of other RNA-protein complexes.

Amino Acid Sequence↗

Structural changes in actin-tropomyosin during muscle regulation: computer modelling of low-angle X-ray diffraction data.

The crystal structure of G-actin monomer has been used together with tropomyosin in a filament model to explain the low-angle X-ray diffraction data from relaxed and activated actin filaments. The four-subdomain actin monomer can be approximated quite well by a four-sphere unit. Orienting this unit and tropomyosin into a filament by searching for the best fit between the computed Fourier transform and the observed vertebrate skeletal muscle low-angle actin layer-lines from muscles at non-overlap sarcomere lengths produced models for the structural changes within the thin filaments (actin plus tropomyosin) between the resting state and the active states, which occur as a result of calcium-activation and independent of myosin interaction with actin. The models are very sensitive to changes in the positions of the centres of mass of the subdomains, but not to the exact shape of the objects used to represent them (e.g. spheres, ellipsoids etc.), as long as the volume is fixed, at the resolution here considered. It is concluded that, even with a four-subdomain structure for the actin molecules, the observed low-angle X-ray diffraction patterns cannot be explained without a substantial azimuthal swing of the tropomyosin strands when resting filaments are calcium-activated. The direction of this swing upon calcium-activation is away from a position close to the proposed major binding site of the myosin head on actin; a result consistent with the original "steric blocking model" of thin filament-based regulation in which the tropomyosin position on actin is crucial for regulation of the myosin crossbridge cycle on actin. Tropomyosin sterically hindering myosin attachment in the "off" state remains a possibility. However, even in the "on" state, the tropomyosin position is close enough to the myosin-binding site to have an effect, where it could regulate the transition of the head from a weak to a strong state. In addition to this tropomyosin movement there are small, but plausible, actin subdomain movements. A tropomyosin shift on its own will not explain the data. Allowance for possible movement of actin subdomain 2 along with the tropomyosin shift still does not explain the data. An additional small movement of subdomain 1; the main myosin-binding subdomain, is postulated.

Actin Cytoskeleton↗

MONSSTER: a method for folding globular proteins with a small number of distance restraints.

The MONSSTER (MOdeling of New Structures from Secondary and TEritary Restraints) method for folding of proteins using a small number of long-distance restraints (which can be up to seven times less than the total number of residues) and some knowledge of the secondary structure of regular fragments is described. The method employs a high-coordination lattice representation of the protein chain that incorporates a variety of potentials designed to produce protein-like behaviour. These include statistical preferences for secondary structure, side-chain burial interactions, and a hydrogen-bond potential. Using this algorithm, several globular proteins (1ctf, 2gbl, 2trx, 3fxn, 1mba, 1pcy and 6pti) have been folded to moderate-resolution, native-like compact states. For example, the 68 residue 1ctf molecule having ten loosely defined, long-range restraints was reproducibly obtained with a C alpha-backbone root-mean-square deviation (RMSD) from native of about 4. A. Flavodoxin with 35 restraints has been folded to structures whose average RMSD is 4.28 A. Furthermore, using just 20 restraints, myoglobin, which is a 146 residue helical protein, has been folded to structures whose average RMSD from native is 5.65 A. Plastocyanin with 25 long-range restraints adopts conformations whose average RMSD is 5.44 A. Possible applications of the proposed approach to the refinement of structures from NMR data, homology model-building and the determination of tertiary structure when the secondary structure and a small number of restraints are predicted are briefly discussed.

Algorithms↗

Three-dimensional reconstruction of icosahedral particles--the uncommon line.

The past few years have seen an explosion in the number of viral structures determined by icosahedral reconstruction from cryoelectron micrographs. The success of this work has depended upon a combination of the high-fidelity but low-contrast information contained in these images with efficient algorithms for determining particle orientation and three-dimensional structure. This review describes the principles behind the most commonly used method of reconstruction of the icosahedral particles and the method's implementation in an icosahedral reconstruction program suite.

Algorithms↗

Computer visualization of three-dimensional image data using IMOD.

We have developed a computer software package, IMOD, as a tool for analyzing and viewing three-dimensional biological image data. IMOD is useful for studying and modeling data from tomographic, serial section, and optical section reconstructions. The software allows image data to be visualized by several different methods. Models of the image data can be visualized by volume or contour surface rendering and can yield quantitative information.

Animals↗

Sterecon--three-dimensional reconstructions from stereoscopic contouring.

Sterecon is a system for making 3-D reconstructions or measurements by tracing from stereopair images. The stereopair images may come directly from a microscope, such as a transmission or scanning electron microscope. Alternatively, the images may be created from a stack of thin slices, such as a confocal light microscopy depth series, an electron tomographic volume, or a set of serial histological slices. When the structure to be studied is thick or complex, a serial stack of stereoscopic images can be used. Objects are traced within the images, and their coordinates are entered into a line or contour database. The contour database can be used for 3-D structure measurement, and the contours can be displayed as a reconstruction. Sterecon has interfaces from other software which can generate the input images and to other software for further display and analysis.

Animals↗

A flexible environment for the visualization of three-dimensional biological structures.

"Ducky" is a flexible and versatile software system for processing, rendering, and animating 3D datasets. The system is based on a powerful run-time interpreted language similar to C. The language includes many built-in functions for animation, rendering, shading, surface definition, and the creation of interactive menu and window-based visualization environments. Both volume and surface rendering methods are provided and may be combined in a single visualization. Ducky can create animations of a sequence of different views of a structure either within a 3D volume or across a series of volumes. Scripts implementing several common visualization tasks are provided. The system is readily extendible. Existing scripts can be modified or new scripts written to create additional interactive environments and processes.

Computer Graphics↗

A model-based approach for determining orientations of biological macromolecules imaged by cryoelectron microscopy.

A polar Fourier transform (PFT) method is described that facilitates determination and refinement of orientations of individual biological macromolecules imaged with cryoelectron microscopy techniques. A three-dimensional density map serves as a high signal-to-noise model from which a PFT database of different views is generated and against which the PFTs of individual images are correlated. The PFT produces rotation-invariant data particularly well-suited for rapid and accurate determination of orientation parameters. The method relies on accurate knowledge of the center of symmetry and radial scale of both model and image data but is insensitive to the relative contrast and background values of these data. Density maps may be derived from a variety of sources such as computer-generated models, X-ray crystallographic structures, and three-dimensional reconstructions computed from images. The PFT technique has been particularly useful for the analysis of particles with icosahedral symmetry and could be adapted for the analysis of single particles of any symmetry for which a crude model exists or can be produced.

Capsid↗

3-D TOP-A software package for the topological analysis of image sequences.

The software package 3-D TOP is a measurement software which has been developed to meet the needs of those who analyze mechanical serial sections in histology and optical sections in laser scanning microscopy. The semiautomatic definition of topological centerlines is the backbone of this software. The three basic advantages in using the concept of topology are (a) resolving ambiguities for surface rendering, (b) flexible definition of objects for automatic identification, labeling, and measurement, and (c) topological quantification of complex forms. A specific application of this software to lung research is demonstrated.

Animals↗

Extensible and object-oriented system Eos supplies a new environment for image analysis of electron micrographs of macromolecules.

To study macromolecular structure by electron microscopy, a highly extensible and object-oriented system has been developed for image analysis. This system is named "Eos" (Extensible and object-oriented system). The system described here supplies an environment with four types of supports: (i) a group of small tools for image analysis, (ii) tools for integration of small tools, such as "Display2," (iii) tools for development, such as "maketool," and (iv) object-oriented libraries for development of new tools. Using Eos, electron micrographs can be analyzed by small tools and integration tools. In addition, Eos can be used to develop new tools based on new ideas because development tool and object-oriented libraries are provided. The examples of implemented small tools for image analysis include three-dimensional reconstruction of objects with helical symmetry, cluster analysis, and contour expression.

Actins↗

Image analysis of helical objects: the Brandeis Helical Package.

Although the fundamental steps in Fourier-based image analysis of electron micrographs of helical structures have not changed significantly since the techniques were developed 30 years ago, there have been developments which aid both the analysis itself and the interpretation of results. Increases in computational resources have allowed the automation of many of the repetitive steps in image processing. We describe here a set of computer programs which have been developed at Brandeis University over the past 10 or more years. These programs, referred to as the Brandeis Helical Package, are designed to operate independently of each other with a simple and more uniform protocol for the flow of information between them. The programs are now easier to understand and to use and therefore represent a good tool for the analysis of helical structures.

Actins↗

Toward fully automated high-resolution electron tomography.

Electron tomography is a powerful tool in elucidating the three-dimensional architecture of large biological complexes and subcellular organelles. Its use can be expanded through the simplification of the tomographic procedure by automation of its tasks. In this paper, we describe our EMACT/EMCAT system, which automates both tomographic data collection and reconstruction.

Animals↗

Automated software package for icosahedral virus reconstruction.

The three-dimensional reconstruction of icosahedral viruses from electron micrograph images has become an important tool for understanding virus structure, function, and pathogenesis. We have developed an integrated suite of software programs to automate most of the operations involved in producing these reconstructions from EM images. Our package combines the analytical capabilities of preexisting algorithms together with approaches we have developed to produce an interactive working environment which enhances the efficiency and usefulness of this approach to the structural analysis of icosahedral viruses.

Algorithms↗

Quantitative fitting of atomic models into observed densities derived by electron microscopy.

A new methodology for fitting atomic models into density distributions is described. This approach is based on a global density correlation analysis that can be optionally supplemented by biochemical as well as biophysical data. The procedure is completely general and enables an objective evaluation of the resulting docking in the light of available biochemical and biophysical information as well as density correlation alone. In this paper we describe the implementation of the algorithm and its application to two biological systems. In both cases the procedure provided an interface model on the atomic level and located parts of the structure that were missing in the atomic model but present in the electron-microscopic construct. It also detected and quantified conformational changes in actomyosin complexes.

Actin Cytoskeleton↗

Situs: A package for docking crystal structures into low-resolution maps from electron microscopy.

Three-dimensional image reconstructions of large-scale protein aggregates are routinely determined by electron microscopy (EM). We combine low-resolution EM data with high-resolution structures of proteins determined by x-ray crystallography. A set of visualization and analysis procedures, termed the Situs package, has been developed to provide an efficient and robust method for the localization of protein subunits in low-resolution data. Topology-representing neural networks are employed to vector-quantize and to correlate features within the structural data sets. Microtubules decorated with kinesin-related ncd motors are used as model aggregates to demonstrate the utility of this package of routines. The precision of the docking has allowed for the extraction of unique conformations of the macromolecules and is limited only by the reliability of the underlying structural data.

Animals↗