Base-dependent competitive adsorption of single-stranded DNA on gold

We characterize the room-temperature adsorption of single-stranded DNA homo-oligonucleotides from solution onto polycrystalline Au films, including competitive adsorption between all possible pairs of unmodified oligomers. Fourier transform infrared (FTIR) and X-ray photoelectron (XPS) spectroscopy analysis of the resulting films shows that oligonucleotides adsorb with a strongly base-dependent affinity, adenine (A) > cytosine (C) >/= guanine (G) > thymine (T). In competitive adsorption experiments on Au, oligo(dA) strongly dominates over the other oligonucleotides. The relative adsorption affinity of oligo(dA) is so great that it competes effectively against adsorption of thiolated oligomers and even causes hybridized oligo(dA).oligo(dT) duplexes to denature in the presence of Au.     

Encoding of polycyclic Si-containing molecules for determining species uniqueness in automated mechanism generation

Automated mechanism generation is an attractive way to understand the fundamental kinetics of complex reaction systems such as silicon hydride clustering chemistry. It relies on being able to tell molecules apart as they are generated. The graph theoretic foundation allows molecules to be identified using unique notations created from their connectivity. To apply this technique to silicon hydride clustering chemistry, a molecule canonicalization and encoding algorithm was developed to handle complex polycyclic, nonplanar species. The algorithm combines the concepts of extended connectivity and the idea of breaking ties to encode highly symmetric molecules. The connected components in the molecules are encoded separately and reassembled using a depth-first search method to obtain the correct string codes. A revised cycle-finding algorithm was also developed to properly select the cycles used for ring corrections when thermodynamic properties were calculated using group additivity. In this algorithm, the molecules are expressed explicitly as trees, and all linearly independent cycles of every size in the molecule are found. The cycles are then sorted according to their size and functionality, and the cycles with higher priorities will be used to include ring corrections. Applying this algorithm, more appropriate cycle selection and more accurate estimation of thermochemical properties of the molecules can be obtained.     

Noise and edge artifacts in maximum-likelihood reconstructions for emission tomography

Images produced in emission tomography with the expectation-maximization algorithm have been observed to become more noisy and to have large distortions near edges as iterations proceed and the images converge towards the maximum-likelihood estimate. It is our conclusion that these artifacts are fundamental to reconstructions based on maximum-likelihood estimation as it has been applied usually; they are not due to the use of the expectation-maximization algorithm, which is but one numerical approach for finding the maximum-likelihood estimate. In this paper, we develop a mathematical approach for suppressing both the noise and edge artifacts by modifying the maximum-likelihood approach to include constraints which the estimate must satisfy.     

Determination of emamectin benzoate in medicated fish feed: a multisite study

A new method was developed for the quantitation of emamectin benzoate in medicated fish feed at levels between 1 and 30 ppm. The new procedure, based on a previously reported assay, consists of a wet methanolic extraction of ground feed, followed by solid-phase extraction and injection onto a gradient liquid chromatographic system. A multisite study involving 3 laboratories (the developing laboratory and 2 independent laboratories) was performed to evaluate precision, recovery, linearity, and sensitivity. Mean recove;ries for triplicate analyses at 3 levels, performed by 2 analysts per laboratory, were between 89 and 97%, with coefficients of variation ranging from 1.6 to 8.6%. Coefficients of determination (r2) obtained from the plotted data were > or =0.993. The precision of the method, determined from 6 replicate preparations from the same batch of medicated feed assayed in 3 separate trials per laboratory, was between 0.6 and 5.8%. The quantitation limit was established at 0.5 ppm. Specificity and robustness studies were performed by the developing laboratory.     

抗人血小板单克隆抗体的研究——Ⅱ.抗血小板糖蛋白Ⅰ单克隆抗体——SZ-2

单克隆抗体SZ-2特异作用于人血小板和巨核细胞,测定10例正常人血小板SZ-2结合位点数为15200±4100/血小板,KD值0.66±0.33nM。SZ-2所识别的抗原对糜蛋白酶敏感,但对神经氨酸酶不敏感,亲和层析技术证明其为血小板糖蛋白Ib(GPIb)。SZ-2与其它抗GPIb单克隆抗体不同,它不仅抑制瑞斯托霉素诱导的血小板聚集,而且也抑制Ⅰ型胶原和血小板活化因子诱导的血小板聚集,并抑制上述诱导剂引起的血小板5-HT和βTG释放。     

Fast, long-range electron-transfer reactions of a "blue" copper protein coupled non-covalently to an electrode through a stilbenyl thiolate monolayer

A self-assembled monolayer (SAM), formed by the insitu saponification of a stilbenyl thioacetate on a gold electrode, yields fast electron transfer (ET)(the exchange rate at zero driving force exceeds 1600 s-1) with adsorbed molecules of the blue copper protein, azurin, over a distance exceeding 15 angstroms .