Identification of a 68 kDa protein which copurifies with type-1 protein phosphatase as albumin

AbstractProteins of 60–70 kDa copurify with some preparations of type-1 or type-2 phosphatases. In our system chromatography on polylysine-Affi-Gel 10 separates a 68 kDa protein from rabbit muscle glycogen particle phosphorylase phosphatase. The separation affects neither the activity nor the size of the phosphatase. The 68 kDa protein, although pure by SDS gel electrophoresis criteria, still displays phosphatase activity of approx. 6–8 Umg. However, rechromatography either on Bio-Gel A-0.5 m or on Blue Sepharose CL-6B followed by gel filtration shows that the activity is due to a contamination with phosphatases of type 1 and type 2, displaying a molecular mass of 35 kDa, which can be totally removed from the 68 kDa protein. The amino acid composition of the 68 kDa protein is identical to that of rabbit serum albumin, within the limits of variation of the method. Furthermore, the sequence of the 38 N-terminal amino acids is the same in the isolated 68 kDa protein and in rabbit serum albumin

Brief Report: Visuo-spatial Guidance of Movement during Gesture Imitation and Mirror Drawing in Children with Autism Spectrum Disorders

Thirteen autistic and 14 typically developing children (controls) imitated hand/arm gestures and performed mirror drawing; both tasks assessed ability to reorganize the relationship between spatial goals and the motor commands needed to acquire them. During imitation, children with autism were less accurate than controls in replicating hand shape, hand orientation, and number of constituent limb movements. During shape tracing, children with autism performed accurately with direct visual feedback, but when viewing their hand in a mirror, some children with autism generated fewer errors than controls whereas others performed much worse. Large mirror drawing errors correlated with hand orientation and hand shape errors in imitation, suggesting that visuospatial information processing deficits may contribute importantly to functional motor coordination deficits in autism

Construction of Parseval wavelets from redundant filter systems

We consider wavelets in L^2(R^d) which have generalized multiresolutions. This means that the initial resolution subspace V_0 in L^2(R^d) is not singly generated. As a result, the representation of the integer lattice Z^d restricted to V_0 has a nontrivial multiplicity function. We show how the corresponding analysis and synthesis for these wavelets can be understood in terms of unitary-matrix-valued functions on a torus acting on a certain vector bundle. Specifically, we show how the wavelet functions on R^d can be constructed directly from the generalized wavelet filters.Comment: 34 pages, AMS-LaTeX ("amsproc" document class) v2 changes minor typos in Sections 1 and 4, v3 adds a number of references on GMRA theory and wavelet multiplicity analysis; v4 adds material on pages 2, 3, 5 and 10, and two more reference

Initial Leakage Under Pit and Fissure Sealants Assessed by Neutron Activation

An improved neutron activation method and a model system were used to study microleakage associated with three pit and fissure sealants. Both the sealant and the etching procedure were evaluated on enamel surfaces as well as in prepared model pits. Leakage was reduced to 3 to 4 μg for all three materials, and the etching process was relatively ineffective in forming an initial seal.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66699/2/10.1177_00220345740530062501.pd

Sawja: Static Analysis Workshop for Java

Static analysis is a powerful technique for automatic verification of programs but raises major engineering challenges when developing a full-fledged analyzer for a realistic language such as Java. This paper describes the Sawja library: a static analysis framework fully compliant with Java 6 which provides OCaml modules for efficiently manipulating Java bytecode programs. We present the main features of the library, including (i) efficient functional data-structures for representing program with implicit sharing and lazy parsing, (ii) an intermediate stack-less representation, and (iii) fast computation and manipulation of complete programs

Identification of a 200 kDa polypeptide as type 3 phosphatidylinositol 4-kinase from bovine brain by partial protein and cDNA sequencing

AbstractTwo phosphatidylinositol 4-kinase isozymes, type 3 and type 2, have been separated on hydroxylapatite after solubilizing bovine brain microsomes with Triton X-114. Employing a newly developed renaturation procedure following SDS-PAGE, we demonstrate that a 200 kDa polypeptide carries the enzymic activity of this type 3 isoform. Chromatography on hydroxylapatite, Heparin-Sepharose, Superdex 200 and finally SDS-PAGE results in an approximately 30000-fold purification. Tryptic peptides generated from the 200 kDa polypeptide after SDS-PAGE have been sequenced and the obtained data have been used for constructing and synthesizing degenerated oligonucleotides. Polymerase chain reaction as well as screening of cDNA libraries allowed several clones to be isolated from which a 4.7 kb contiguous sequence can be built up. The open reading frame covers 4.4 kb with a 0.3 kb untranslated 3' end which yields a deduced amino acid sequence of 1,467 amino acids. The C-terminal part of ca. 300 amino acids represents the catalytic domain. Sequence alignment of this domain with the mammalian counterpart, the human type 2 phosphatidylinositol 4-kinase, the yeast kinases STT4 and PIK1, as well as with the catalytic domains of bovine, human, mouse and yeast phosphatidylinositol 3-kinases reveals a high degree of identity: 26 of these approximately 300 amino acids are invariable in all of these eight catalytic domains. Five motifs indicate nuclear localization and DNA binding properties of the enzyme. Two leucine zipper motifs (amino acids 358–386, 862–882) are detectable. Furthermore, a helix loop helix motif (amino acids 716–729) as well as two nuclear localization signals (amino acids 838–854, 345–349) indicate the presence of the type 3 isoform in the nucleus

Orthonormal sequences in L2(Rd)L^2(R^d) and time frequency localization

We study uncertainty principles for orthonormal bases and sequences in $L^2(\R^d)$. As in the classical Heisenberg inequality we focus on the product of the dispersions of a function and its Fourier transform. In particular we prove that there is no orthonormal basis for $L^2(\R)$ for which the time and frequency means as well as the product of dispersions are uniformly bounded. The problem is related to recent results of J. Benedetto, A. Powell, and Ph. Jaming. Our main tool is a time frequency localization inequality for orthonormal sequences in $L^2(\R^d)$. It has various other applications.Comment: 18 page

Pionic Atoms as Compound States in Nucleon-Nucleus Collisons: Status Report on the Cooler Experiment CE02

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

Measurement of the Total Cross Section for the Reaction p + p → p + p + pio

This research was sponsored by the National Science Foundation Grant NSF PHY-931478

Shear viscosity of the Quark-Gluon Plasma from a virial expansion

We calculate the shear viscosity $\eta$ in the quark-gluon plasma (QGP) phase within a virial expansion approach with particular interest in the ratio of $\eta$ to the entropy density $s$, i.e. $\eta/s$. The virial expansion approach allows us to include the interactions between the partons in the deconfined phase and to evaluate the corrections to a single-particle partition function. In the latter approach we start with an effective interaction with parameters fixed to reproduce thermodynamical quantities of QCD such as energy and/or entropy density. We also directly extract the effective coupling \ga_{\rm V} for the determination of $\eta$. Our numerical results give a ratio $\eta/s\approx 0.097$ at the critical temperature $T_{\rm c}$, which is very close to the theoretical bound of $1/(4\pi)$. Furthermore, for temperatures $T\leq 1.8 T_{\rm c}$ the ratio $\eta/s$ is in the range of the present experimental estimates $0.1-0.3$ at RHIC. When combining our results for $\eta/s$ in the deconfined phase with those from chiral perturbation theory or the resonance gas model in the confined phase we observe a pronounced minimum of $\eta/s$ close to the critical temperature $T_{\rm c}$.Comment: Published in Eur. Phys. J. C, 7 pages, 2 figures, 3 tabl