不完全伽玛函数在描述乳牛泌乳曲线中的应用

论述了不完全伽玛函数拟合奶牛的沁乳曲线,推导了泌乳曲线的数学方程,实例检验的效果良好,就如何应用进行了讨论。     

POLYPEPTIDE CHAINS OF RABBIT GAMMAGLOBULIN

Rabbit gamma globulin has been extensively reduced, and its polypeptide chains separated by gel filtration on Sephadex G-200 in SM guanidine hydrochloride. The larger H (or A) chains make up two-thirds of the molecule and have a molecular weight of approximately 55,000 each. The smaller L (or B) chains account for the other one-third and have a molecular weight of approximately 25,000 each. The data are consistent with a model of the gamma globulin molecule that has two H and two L chains.     

Inv(1) allotype: effect of immunoglobulin G heavy chain subtype on its expression

More protein is required to detect the Inv(1) antigen carried in the light chain of immunoglobulin G molecules when the light chain is combined with a gamma2 heavy chain than when it is combined with a gamma1 or gamma3 heavy chain. One of the four gamma2 heavy chains used in the experiment, however, was as efficient as the gamma1 and gamma3 chains, indicating that there may be two subtypes of gamma2. Inv(1) was more easily detected in one of the two light chains used in the experiment. This difference may be associated with the subtypes of the kappa chain derived from studies of the variable portion of the chain.     

加速重离子辐射对玉米的诱变效应

用不同剂量的3种高传能线密度的加速重离子氖—20、氩—40及铁—56,与低传能线密度的钴—60γ射线分别照射具标志基因(Lw_1/Iw_1)的玉米干种子,以当代植株叶片黄白条纹产生频率为指标,比较其诱发效应。结果表明:在所用剂量范围内,此4种辐射的剂量—效应关系曲线为直线。氖—20、氩—40及铁—56重离子束对应于钴—60γ射线的相对生物学效应分别为2.02、8.31和12.45。叶片具黄白条纹的植株自交,后代仍有黄白条纹。光学显微镜及透射电子显微镜观察发现黄白条纹部位的叶肉细胞及其内的叶绿体形态结构明显不同于正常绿叶。     

重离子辐射诱导水稻花粉母细胞染色体畸变的研究

分别用高能重离子４０Ａｒ，５６Ｆｅ，与６０Ｃｏ－γ射线照射水稻边皮占干种子，观察Ｍ１，Ｍ２的发长发充及花粉母细胞减数分裂各时期出现的染色体畸变。结果表明Ｍ１结实率与染色体畸变率均与辐射剂量显著相关。重离子辐射比γ射线更有效减少结实率及诱导染色体畸变，Ｍ１成苗率与结实率及Ｍ１，Ｍ２花粉母细胞染色体畸变率的相对生物学效应值均大于１。Ｍ２花粉母细胞染色体畸变率较低，但仍与剂量呈线性关系，且γ射线诱导畸变     

山羊板皮辐射灭菌

 报道了山羊板皮辐射灭菌工艺的技术指标。研究结果表明：炭疽杆菌芽孢的辐照致死剂量为8KGY。根据不同菌种、株的辐射抗力测定结果，提出了在灭菌工艺中应用无毒指标菌的不同监测标准：短小杆菌“E601”的阴性培养率达到85%即可；蜡状杆菌“4001”则要求达95%；而枯草杆菌黑色变种“8017”则要求不得检出。研究表明，辐照30KGY剂量的山羊板皮对品质无影响。试验还对山羊板皮出口标准包对剂量减弱情况进行了测量，提供了灭菌工艺中的剂量控制参数。     

Molecular weight of human gamma interferon is similar to that of other human interferons

The molecular weight (as determined by molecular sieve chromatography) of human gamma interferon, formerly referred to as immune or type II interferon, is between 40,000 and 70,000. On sodium dodecyl sulfate-polyacrylamide gel electrophoresis, gamma interferon activity was recovered mainly from two regions of the gels corresponding to molecular weights of 20,000 and 25,000. The results suggest that in native form human gamma interferon may be aggregated.     

Immunochemical proof that a novel rearranging gene encodes the T cell receptor delta subunit

The T cell receptor (TCR) delta protein is expressed as part of a heterodimer with TCR gamma, in association with the CD3 polypeptides on a subset of functional peripheral blood T lymphocytes, thymocytes, and certain leukemic T cell lines. A monoclonal antibody directed against TCR delta was produced that binds specifically to the surface of several TCR gamma delta cell lines and immunoprecipitates the TCR gamma delta as a heterodimer from Triton X-100 detergent lysates and also immunoprecipitates the TCR delta subunit alone after chain separation. A candidate human TCR delta complementary DNA clone (IDP2 O-240/38), reported in a companion paper, was isolated by the subtractive library approach from a TCR gamma delta cell line. This complementary DNA clone was used to direct the synthesis of a polypeptide that is specifically recognized by the monoclonal antibody to TCR delta. This complementary DNA clone thus corresponds to the gene that encodes the TCR delta subunit.     

Cytological effects of different mutagens in soybean [Glycine max (L.) Merrill]

The effect of gamma rays, ethyl methane sulphonate, and their three combinations on various cytological parameters in M1 generation was studied in two soybean cultivars, Pusa-16 and PK-1042. Combined treatments exhibited high meiotic abnormalities in Pusa-16 as compared with the individual treatments of ethyl methane sulphonate and gamma rays. In PK-1042 the highest frequency of meiotic abnormalities was exhibited by gamma rays, while in Pusa-16 the frequencies of univalents were high as compared with other meiotic abnormalities. Fragments/bridges, laggards, ring and rod bivalents were other types of meiotic abnormalities that were noticed in both the cultivars. The frequencies of irregular cells in the two cultivars were high in combined treatments followed by ethyl methane sulphonate and gamma rays. The highest percentage of pollen sterility was exhibited by the combined treatments and the lowest was exhibited by gamma rays. In Pusa-16, the increase in doses of gamma rays and ethyl methane sulphonate increased the pollen sterility percentage, while in the combined treatments, the increase was noticed up to the intermediate dose and then gradually decreased at higher doses. On the other hand, in PK-1042 the increase in ethyl methane sulphonate dose increased sterility percentage, while no definite trend was noticed in gamma rays and combined treatments.     

Detection of pulsed gamma rays above 100 GeV from the Crab pulsar

We report the detection of pulsed gamma rays from the Crab pulsar at energies above 100 giga-electron volts (GeV) with the Very Energetic Radiation Imaging Telescope Array System (VERITAS) array of atmospheric Cherenkov telescopes. The detection cannot be explained on the basis of current pulsar models. The photon spectrum of pulsed emission between 100 mega-electron volts and 400 GeV is described by a broken power law that is statistically preferred over a power law with an exponential cutoff. It is unlikely that the observation can be explained by invoking curvature radiation as the origin of the observed gamma rays above 100 GeV. Our findings require that these gamma rays be produced more than 10 stellar radii from the neutron star.     

Type-specific regulation of adenylyl cyclase by G protein beta gamma subunits

Heterotrimeric guanine nucleotide-binding regulatory proteins (G proteins) dissociate into guanosine triphosphate (GTP)-bound alpha subunits and a complex of beta and gamma subunits after interaction with receptors. The GTP-alpha subunit complex activates appropriate effectors, such as adenylyl cyclase, retinal phosphodiesterase, phospholipase C, and ion channels. G protein beta gamma subunits have been found to have regulatory effects on certain types of adenylyl cyclase. In the presence of Gs alpha, the alpha subunit of the G protein that activates adenylyl cyclase, one form of adenylyl cyclase was inhibited by beta gamma, some forms were activated by beta gamma, and some forms were not affected by beta gamma. These interactions suggest mechanisms for communication between distinct signal-transducing pathways.     

Activation of gamma delta T cells in the primary immune response to Mycobacterium tuberculosis

Although the immunologic role of T cells bearing the conventional alpha beta T cell receptor (TCR) has been well characterized, little is known about the function of the population of T cells bearing the gamma delta TCR. Therefore, the role of gamma delta T cells in the immune response to Mycobacterium tuberculosis (MT) was investigated. The number of TCR gamma delta cells in the draining lymph nodes of mice immunized with MT was greatly increased in comparison with the number of TCR alpha beta cells. Three biochemically distinct gamma delta TCRs were detected. Analyses of cell cycle, of interleukin-2 receptor expression, and of interleukin-2 responsiveness showed that a large proportion of the gamma delta T cells were activated in vivo. TCR gamma delta cells responded to solubilized MT antigens in vitro but, in contrast to MT-specific alpha beta T cells, the response of gamma delta T cells to MT did not require major histocompatability complex class II recognition. These results provide an example of antigen-specific activation of gamma delta T cells in vivo and indicate that gamma delta T cells may have a distinct role in generating a primary immune response to certain microorganisms.     

Activation of muscarinic potassium currents by ATP gamma S in atrial cells

Intracellular perfusion of atrial myocytes with adenosine 5'-(gamma-thio) triphosphate (ATP gamma S), an ATP analog, elicits a progressive increase of the muscarinic potassium channel current, IK(M), in the absence of agonists. In this respect, ATP gamma S mimics the actions of guanosine triphosphate (GTP) analogs, which produce direct, persistent activation of the guanyl nucleotide-binding (G) protein controlling the K+(M) channel. The effect of ATP gamma S on IK(M), however, differs from that produced by GTP analogs in two aspects: it requires relatively large ATP gamma S concentrations, and it appears after a considerable delay, suggesting a rate-limiting step not present in similar experiments performed with guanosine 5'-(gamma-thio) triphosphate (GTP gamma S). Incubation of atrial homogenates with [35S]ATP gamma S leads to formation of significant amounts of [35S]GTP gamma S, suggesting that activation of IK(M) by ATP gamma S arises indirectly through its conversion into GTP gamma S by cellular enzymes. ATP gamma S is often used to demonstrate the involvement of protein phosphorylation in the control of various cellular processes. The finding that cytosolic application of ATP gamma S can also lead to G-protein activation implies that experiments with ATP gamma S must be interpreted with caution.     

Radioresistance of cooperative function of carrier-specific lymphocytes in antihapten antibody responses

Transfer of lymphoid cells from strain-2 guinea pigs immunized to bovine gamma globulin into syngeneic recipients immunized with dinitrophenyl ovalbumin markedly enhances the secondary antidinitrophenyl response of the recipient to challenge with dinitrophenyl-bovine gamma globulin. This function of the carrier bovine gamma globulin-specific cells is resistant to irradiation with up to 5000 rads, although the capacity of the irradiated cell population to transfer immunologic memory for bovine gamma globulins or to be stimulated by antigen to synthesize DNA in vitro is abolished by this treatment.     

Characterization of T cell receptor gamma chain expression in a subset of murine thymocytes

While much information exists about the structure and function of the clonally distributed T cell receptor (TCR) alpha beta heterodimer, little is known about the gamma protein, the product of a third rearranging TCR gene. An antiserum to a carboxyl-terminal peptide common to several of the murine gamma chain constant regions and a monoclonal antibody to the murine T3 complex were used to identify products of this TCR gene family in a subpopulation of Lyt2-, L3T4- thymocytes. This subpopulation does not express TCR alpha or full-length TCR beta messenger RNA. The gamma chain is a 35-kilodalton (kD) protein that is disulfide-bonded to a 45-kD partner and is associated with the T3 complex. Analysis of the glycosylation pattern of this thymic gamma chain revealed that the major variable region gamma (V gamma) gene transcribed in activated peripheral T cells is absent from this subpopulation. The cells that bear this second T cell receptor may therefore represent a distinct lineage differentiating within the thymus.     

Saturation of cubic optical nonlinearity in long-chain polyene oligomers

The scaling of the cubic nonlinearity gamma with chain length in polyenic molecules has received considerable theoretical attention. Earlier experimental investigations have been restricted to oligomers with fewer than 20 double bonds because of problems associated with the synthesis and solubility of conjugated molecules. These synthetic difficulties have been overcome in the present study by the use of modern living polymerization techniques. Solution measurements of gamma as a function of chain length in long-chain (up to 240 double bonds) model polyene oligomers are reported. A saturation of the increase of gamma with chain length is observed, and the onset of this saturation occurs for chain lengths considerably longer than predicted from theory.     

Binding of SH2 domains of phospholipase C gamma 1, GAP, and Src to activated growth factor receptors

Phospholipase C gamma 1 (PLC gamma 1) and p21ras guanosine triphosphatase (GTPase) activating protein (GAP) bind to and are phosphorylated by activated growth factor receptors. Both PLC gamma 1 and GAP contain two adjacent copies of the noncatalytic Src homology 2 (SH2) domain. The SH2 domains of PLC gamma 1 synthesized individually in bacteria formed high affinity complexes with the epidermal growth factor (EGF)- or platelet derived growth factor (PDGF)-receptors in cell lysates, and bound synergistically to activated receptors when expressed together as one bacterial protein. In vitro complex formation was dependent on prior growth factor stimulation and was competed by intracellular PLC gamma 1. Similar results were obtained for binding of GAP SH2 domains to the PDGF-receptor. The isolated SH2 domains of other signaling proteins, such as p60src and Crk, also bound activated PDGF-receptors in vitro. SH2 domains, therefore, provide a common mechanism by which enzymatically diverse regulatory proteins can physically associate with the same activated receptors and thereby couple growth factor stimulation to intracellular signal transduction pathways.