Strategies of loop recombination in ciliates

The concept of breakpoint graph, known from the theory of sorting by reversal, has been successfully applied in the theory of gene assembly in ciliates. We further investigate its usage for gene assembly, and show that the graph allows for an efficient characterization of the possible orders of loop recombination operations (one of the three types of molecular operations that accomplish gene assembly) for a given gene during gene assembly. The characterization is based on spanning trees within a graph built upon the connected components in the breakpoint graph. We work in the abstract and more general setting of so-called legal strings.     

Application of pulsed-magnetic field enhances non-viral gene delivery in primary cells from different origins

Primary cell lines are more difficult to transfect when compared to immortalized/transformed cell lines, and hence new techniques are required to enhance the transfection efficiency in these cells. We isolated and established primary cultures of synoviocytes, chondrocytes, osteoblasts, melanocytes, macrophages, lung fibroblasts, and embryonic fibroblasts. These cells differed in several properties, and hence were a good representative sample of cells that would be targeted for expression and delivery of therapeutic genes in vivo. The efficiency of gene delivery in all these cells was enhanced using polyethylenimine-coated polyMAG magnetic nanoparticles, and the rates (17–84.2%) surpassed those previously achieved using other methods, especially in cells that are difficult to transfect. The application of permanent and pulsating magnetic fields significantly enhanced the transfection efficiencies in synoviocytes, chondrocytes, osteoblasts, melanocytes and lung fibroblasts, within 5 min of exposure to these magnetic fields. This is an added advantage for future in vivo applications, where rapid gene delivery is required before systemic clearance or filtration of the gene vectors occurs.     

A two-dimensional matrix Padé-type approximation in the inner product space

By introducing a bivariate matrix-valued linear functional on the scalar polynomial space, a general two-dimensional (2-D) matrix Padé-type approximant (BMPTA) in the inner product space is defined in this paper. The coefficients of its denominator polynomials are determined by taking the direct inner product of matrices. The remainder formula is developed and an algorithm for the numerator polynomials is presented when the generating polynomials are given in advance. By means of the Hankel-like coefficient matrix, a determinantal expression of BMPTA is presented. Moreover, to avoid the computation of the determinants, two efficient recursive algorithms are proposed. At the end the method of BMPTA is applied to partial realization problems of 2-D linear systems.     

An exact and polynomial distance-based algorithm to reconstruct single copy tandem duplication trees

The problem of reconstructing the duplication tree of a set of tandemly repeated sequences which are supposed to have arisen by unequal recombination, was first introduced by Fitch (1977), and has recently received a lot of attention. In this paper, we place ourselves in a distance framework and deal with the restricted problem of reconstructing single copy duplication trees. We describe an exact and polynomial distance based algorithm for solving this problem, the parsimony version of which has previously been shown to be NP-hard (like most evolutionary tree reconstruction problems). This algorithm is based on the minimum evolution principle, and thus involves selecting the shortest tree as being the correct duplication tree. After presenting the underlying mathematical concepts behind the minimum evolution principle, and some of its benefits (such as statistical consistency), we provide a new recurrence formula to estimate the tree length using ordinary least-squares, given a matrix of pairwise distances between the copies. We then show how this formula naturally forms the dynamic programming framework on which our algorithm is based, and provide an implementation in O(n³) time and O(n²) space, where n is the number of copies.     

对称常微分算子的两种自伴延拓形式之间的联系

建立了对称常微分算子von N eum ann自伴延拓与以边条件形式表达的自伴延拓之间的对应关系,给出了相互转换的方法.     

损伤材料裂纹尖端附近的应力场

本文导出了损伤材料的全量理论,导出了全量公式中H的渐近表达式;最后得到损伤材料平面应变条件下的裂纹尖端的应力应变场。     

Indirect ultrasonication for protein quantification and peptide mass mapping through mass spectrometry-based techniques

We report in this work a fast protocol for protein quantification and for peptide mass mapping that rely on ¹⁸O isotopic labeling through the decoupling procedure. It is demonstrated that the purity and source of trypsin do not compromise the labeling degree and efficiency of the decoupled labeling reaction, and that the pH of the labeling reaction is a critical factor to obtain a significant ¹⁸O double labeling. We also show that the same calibration curve can be used for MALDI protein quantification during several days maintaining a reasonable accuracy, thus simplifying the handling of the quantification process. In addition we demonstrate that ¹⁸O isotopic labeling through the decoupling procedure can be successfully used to elaborate peptide mass maps. BSA was successfully quantified using the same calibration curve in different days and plasma from a freshwater fish, Cyprinus carpio, was used to elaborate the peptide mass maps.     

Trace LC/MS/MS quantitation of 17β‐estradiol as a biomarker for selective estrogen receptor modulator activity in the rat brain

A sensitive LC/MS/MS method has been developed by derivatization of 17β‐estradiol (E2) with dansyl chloride to quantitate 17β‐E2 in female rat serum. The use of E2‐d₅ minimized interferences from endogenous 17β‐E2 in order to achieve a limit of quantitation (LOQ) of 2.5 pg/ml using 150 µl of female rat serum. The recovery of the dansyl derivative was 95% or greater in quality control samples. The intra and interday assay precision was better than 8.2 and 6.2%, respectively, with accuracies ranging from 97 to 101% in the quality control samples. The assay was used for the quantitation of serum E2 as a biomarker for the estrogen receptor (ER) antagonist activity of small molecule SERMs (selective estrogen receptor modulators) in the female rat brain. The study revealed that a statistically significant upregulation of serum 17β‐E2 occurred for rats dosed with SERMs that are known to penetrate the brain and disrupt the hypothalamic‐pituitary‐ovarian (HPO) axis. Variations in 17β‐E2 in ascending dose studies also correlated with the corresponding trends in CYP17a1 levels, an mRNA biomarker for ovarian hyperstimulation. This biomarker assay has provided a useful screen for medicinal chemistry optimization to produce SERMs that do not interfere with negative feedback of estrogens on the brain and for biological hypothesis testing. Copyright © 2009 John Wiley & Sons, Ltd.