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Conformation array

Figure 1 In the array-of-arrays conformation a standard microscope slide is divided into 80 subarrays with a diameter identical to that of a 384-well-microtiter-plate reaction well, schematically illustrated to the left in the image. Up to 200 oligonucleotide spots can be printed per subarray at a center-to-center distance of 200 pm. With the possibility to analyze 80 samples in parallel, up to 16,000 genotypes per slide can be generated. Fluorescence images of four reaction wells, where the minisequencing reaction have been performed are shown to the right. Figure 1 In the array-of-arrays conformation a standard microscope slide is divided into 80 subarrays with a diameter identical to that of a 384-well-microtiter-plate reaction well, schematically illustrated to the left in the image. Up to 200 oligonucleotide spots can be printed per subarray at a center-to-center distance of 200 pm. With the possibility to analyze 80 samples in parallel, up to 16,000 genotypes per slide can be generated. Fluorescence images of four reaction wells, where the minisequencing reaction have been performed are shown to the right.
Here each entry denotes a subarray and is shown accordingly in bold type. Thus, the vector x is partitioned here into two subvectors, and the matrix A is partitioned into six submatrices. The submatrix Ahk contains the coefficients in the row subset h for the elements of the subvector Xk, thus, these arrays conform for multiplication in the order written. [Pg.180]

J. I. Simon, Impedance Properties of Periodic Linear Arrays Conformal to a Dielectric-Clad Infinite PEC Cylinder, Ph.D. Dissertation, Ohio State University, Department of Electrical Engineering, Columbus, OH, 1989. [Pg.389]

The Diels-Alder cycloaddition is one example of a pencyclic reaction, which is a one step reaction that proceeds through a cyclic transition state Bond formation occurs at both ends of the diene system and the Diels-Alder transition state involves a cyclic array of six carbons and six tt electrons The diene must adopt the s cis conformation m the transition state... [Pg.409]

Richmond and collaborators (Figure 12.30). The octamer (Figure 12.29) has surface landmarks that guide the course of the DNA around the octamer 146 bp of B-DNA in a flat, left-handed superhelical conformation make 1.65 turns around the histone core (Figure 12.30), which itself is a protein superhelix consisting of a spiral array of the four histone dimers. Histone 1, a three-domain protein, serves to seal the ends of the DNA turns to the nucleosome core and to organize the additional 40 to 60 bp of DNA that link consecutive nucleo-... [Pg.380]

Recent advances of the Seeman group led to the construction of a nanomechanical device from DNA [89]. In this molecular apparatus, the ion-dependent transition of B-DNA into the Z-conformation is used to alter the distance between two DNA DX domains attached to the switchable double helix. Atomic displacements of about 2-6 nm were attained. Ionic switching of nanoparticles by means of DNA supercoiling has also been reported [53]. Additional advances regarding the use of DNA is nanomechanical devices have been reported by Fritz et al., who showed that an array of cantilevers can be used to... [Pg.410]

Sarcoplasmic reticulum vesicles prepared from rabbit skeletal muscle were crystallized in a medium of 0.1 M KCl, lOmM imidazole (pH 8), and 5mM MgCl2 by the addition of either CaCl2 (100/rM) or lanthanide ions (1-8 M) that stabilize the E conformation of the Ca -ATPase [119]. After incubation at 2°C for 5-48 hours, crystalline arrays were observed on the surface of about 10 20% of the vesicles in sarcoplasmic reticulum preparations obtained from fast-twitch rabbit skeletal muscles. [Pg.73]

Molecules of the simpUcity of ethane or the complexity of proteins and DNA adopt different conformations. In the case of ethane this gives rise to the notion of a staggered and eclipsed bond, whereas proteins form an array of complex structural elements and DNA - the famous double hehx. The understanding of the conformational properties of small molecules is an important factor in computational approaches contributing to drug discovery. [Pg.183]

Historically, research on polypeptide structure, whether by experimental or computational means, has focused on the folded state only. This is because an array of methods exist for detailed investigation of the folded state of a polypeptide, and because the folded state is commonly the functionally active one. There are, however, two scenarios in which a full characterization of the unfolded state becomes as essential as the determination of the folded conformation. The first is in the study of... [Pg.364]

N,A -bis(2-phyidylmethyl)pyrazine-2,3-dicarboxamide was crystallized in two orthorhombic forms, which differ from each other in the conformational arrangements of the compound [44], A new polymorph of 2-bromo-5-hydroxybenzaldehyde has been reported where a pair of hydrogen bonds linked molecules related by a center of inversion [45], One of the intermediates important in the synthesis of an antituberculosis drug, methyl p-aminobenzoate, was found to crystallize in a new monoclinic polymorph where molecules were arranged in head-to-tail linear ribbon arrays [46]. [Pg.269]

Traditional methods for fabricating nano-scaled arrays are usually based on lithographic techniques. Alternative new approaches rely on the use of self-organizing templates. Due to their intrinsic ability to adopt complex and flexible conformations, proteins have been used to control the size and shape, and also to form ordered two-dimensional arrays of nanopartides. The following examples focus on the use of helical protein templates, such as gelatin and collagen, and protein cages such as ferritin-based molecules. [Pg.174]


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