Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis (CF) is a common lethal genetic disease that manifests itself in airway and other epithelial cells as defective chloride ion absorption and secretion, resulting at least in part from a defect in a cyclic AMP-regulated, outwardly-rectifying Cl- channel in the apical surface. The gene responsible for CF has been identified and predicted to encode a membrane protein termed the CF transmembrane conductance regulator (CFTR). Identification of a cryptic bacterial promoter within the CFTR coding sequence led us to construct a complementary DNA in a low-copy-number plasmid, thereby avoiding the deleterious effects of CFTR expression on Escherischia coli. We have used this cDNA to express CFTR in vitro and in vivo. Here we demonstrate that CFTR is a membrane-associated glycoprotein that can be phosporylated in vitro by cAMP-dependent protein kinase. Polyclonal and monoclonal antibodies directed against distinct domains of the protein immunoprecipitated recombinant CFTR as well as the endogenous CFTR in nonrecombinant T84 cells. Partial proteolysis fingerprinting showed that the recombinant and non-recombinant proteins are indistinguishable. These data, which establish several characteristics of the protein responsible for CF, will now enable CFTR function to be studied and will provide a basis for diagnosis and therapy.     

Cloning of a cDNA encoding a non-isopeptide-selective subtype of the endothelin receptor

Endothelin-1 was initially identified as a 21-residue potent vasoconstrictor peptide produced by vascular endothelial cells, but was subsequently found to have many effects on both vascular and non-vascular tissues. The discovery of three isopeptides of the endothelin family, ET-1, ET-2 and ET-3, each possessing a diverse set of pharmacological activities of different potency, suggested the existence of several different endothelin receptor subtypes. Endothelins may elicit biological responses by various signal-transduction mechanisms, including the G protein-coupled activation of phospholipase C and the activation of voltage-dependent Ca2+ channels. Thus, different subtypes of the endothelin receptor may use different signal-transduction mechanisms. Here we report the cloning of a complementary DNA encoding one subtype belonging to the superfamily of G protein-coupled receptors. COS-7 cells transfected with the cDNA express specific and high-affinity binding sites for endothelins, responding to binding by the production of inositol phosphates and a transient increase in the concentration of intracellular free Ca2+. The three endothelin isopeptides are roughly equipotent in displacing 125I-labelled ET-1 binding and causing Ca2+ mobilization. A messenger RNA corresponding to the cDNA is detected in many rat tissues including the brain, kidney and lung but not in vascular smooth muscle cells. These results indicate that this cDNA encodes a 'nonselective' subtype of the receptor which is different from the vascular smooth muscle receptor.     

Molecular cloning of the microtubule-associated mechanochemical enzyme dynamin reveals homology with a new family of GTP-binding proteins

A complementary DNA encoding the D100 polypeptide of rat brain dynamin--a force-producing, microtubule-activated nucleotide triphosphatase--has been cloned and sequenced. The predicted amino acid sequence includes a guanine nucleotide-binding domain that is homologous with those of a family of antiviral factors, inducible by interferon and known as Mx proteins, and with the product of the essential yeast vacuolar protein sorting gene VPS1. These relationships imply the existence of a new family of GTPases with physiological roles that may include microtubule-based motility and protein sorting.     

s-单式环的交换性定理(英文)

本文将文献[3]的引理1推广到s-单式环上,并用迭代技术给出文献[4]的定理2一个简易的证明,将若干有1环的交换性定理推广到s-单式环上。     

溅射用铁电陶瓷靶的烧结与显微结构分析

探讨了溅射用铁电陶瓷靶（ＰＺＴ，ＰＬＺＴ）的烧结工艺，并对其显微结构进行了分析。结果表明，采用新的烧结工艺（含保护措施），可以有效地抑制ＰｂＯ的挥发，制备出组织结构及成分均匀、ＰｂＯ含量正常、致密度较高、不变形的符合磁控溅射要求的铁电陶瓷烧结靶。     

时间序列AR模型参数的积分求解法

基于对时间序列实质的分析，提出了旨在减少序列的随机误差影响以及提高拟合精度的ＡＲ模型参数的积分求解法．重点讨论了ＡＲ（１）模型及ＡＲ（ｐ）模型参数的积分求解法，并与最小二乘法在计算机上进行了仿真比较．结果表明，采用积分求解法所得的ＡＲ模型参数的估计精度比最小二乘法的高．     

剩余静校正的小波包预处理方法

强反射层追踪与相对时差拾取中的“多值”现象严重影响剩余静校正的效果，为此提出的小波包预处理方法，可以实现地震道噪声与信号及不同强反射层的分离，从而能自动识别并提取“纯”的强反射层，提高强反射层追踪的可靠性和相对时差的拾取精度．     

PWM逆变电源抗冲击负荷电路研究

对几种逆变电源的抗冲击性负荷电路进行分析，给出了一种便于实现且效果很好的电路，实验证明此电路对各种冲击负荷甚至输出短路都能进行很好的限流，可以彻底解决逆变电源在负载冲击下频繁停机的问题。