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971.
Topology of MDR1-P-glycoprotein as indicated by epitope mapping of monoclonal antibodies to human MDR cells 总被引:1,自引:0,他引:1
Maurizio Cianfriglia Francesca Poloni Claudia Signoretti Giulia Romagnoli Marina Tombesi Franco Felici 《Cytotechnology》1996,19(3):247-251
The MDR1-P-glycoprotein binding sites of three different murine monoclonal antibodies (MM4.17, MM6.15 and MC57), directed towards living, intact human multidrug-resistant cells were investigated in order to study P-glycoprotein topology. By using synthetic peptide scanning, we demonstrated that well-defined regions localized on the predicted first, fourth and sixth extracellular loops are external. On the basis of the structure of MM6.15 epitope, which is distributed on the above three different extracellular loops (and thus is discontinuous), P-glycoprotein molecules result to be differently organized in the lipid bilayer. Moreover, the outcome of the MC57 and MM4.17 epitopes localization experiments, obtained through the use of phage-displayed peptide libraries, represent an additional challenge to the classical 12-transmembrane domain model of P-glycoprotein, since they agree with the novel topography of the molecule (10-transmembrane domain), which was recently proposed on the basis of biochemical and expression studies. 相似文献
972.
An overview of the status of the human obesity gene map up to October 1995 is presented. The evidence is drawn from several lines of clinical and experimental research. First, 12 loci linked to Mendelian disorders exhibiting obesity as one clinical feature are reviewed. Second, six loci causing obesity in rodent models of the disease are considered. Third, eight chromosomal regions where quantitative trait loci, identified by crossbreeding experiments with informative strains of mice, are defined. Fourth, 10 candidate genes exhibiting a statistical association with BMI or body fat are introduced. Fifth, nine loci found to be linked to a relevant phenotype are listed and the four cases for which the evidence for linkage is strongest are emphasized. The latter are mapped to 2p25, 6p21.3, 7q33 and 20q12-13.11. Finally, the studies that have concluded that there was no association or linkage with a marker or gene are also reviewed. It is recommended that a system be developed by the obesity research community to ensure that an accurate and easily accessible computerized version of the human obesity gene map becomes available in the near future. 相似文献
973.
Nikolai Friesen Nikolai Borisjuk Ted H. M. Mes Manfred Klaas Peter Hanelt 《Plant Systematics and Evolution》1997,206(1-4):317-335
The tetraploidAllium altyncolicum (2n = 4x = 32) is considered to be of hybrid origin, because most of its morphological characters are intermediate between those of its putative parents,A. schoenoprasum andA. ledebourianum. In the present work an attempt has been made to ascertain its parentage by several methods: Giemsa C-banding, genomic in situ hybridization (GISH), PCR-RFLP of cpDNA, restriction enzyme mapping of the rDNA, and RAPDs. C-banding and GISH indicates clearly thatA. altyncolicum is a segmental allopolyploid.Allium schoenoprasum andA. ledebourianum are the most likely the parental species and the larger part of the genome ofA. altyncolicum (26 chromosomes) is derived fromA. schoenoprasum. The low genetic divergence between these three species was confirmed by the lack of sequence variation in the ITS sequences of nuclear rRNA genes and of the plastid rbcL-atpB intergenic spacer. Both parental species andA. altyncolicum could be distinguished by RFLP of the rDNA repeats. The geographic origin of the putative parental species was investigated using RAPDs.Dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday 相似文献
974.
光敏核不育水稻农垦58S与正常品种“农垦58”在pmsl区段无育性基因分离 总被引:1,自引:0,他引:1
光敏核不育水稻农垦58S系由正常品种“农垦58”(Oryza sativa L.ssp.japonica)自然突变产生。为弄清该突变基因在染色体上的位置,曾用覆盖整个水稻基因组的300余个RFLP探针对农垦58S和“农垦58”进行了对比分析,得到了7个具多态性的探针,其中2个探针RG30和RZ626正好落在第7染色体上以前定位的光敏核不育基因pmsl所在的区段。以这两个标记对农垦58S/“农垦58”组合F_2随机群体140单株进行了RFLP分析,按RFLP基因型分组对育性作方差分析,结果表明,这2个标记位点与此群体中引起育性分离的位点无连锁关系。说明由正常“农垦58”变为光敏核不育农垦58S的突变基因不在pmsl区段。 相似文献
975.
Constantinos Sakarellos Vassilios Tsikaris Eugenia Panou-Pomonis Charalampos Alexopoulos Maria Sakarellos-Daitsiotis Constantinos Petrovas Panayiotis G. Vlachoyiannopoulos Haralampos M. Moutsopoulos 《Letters in Peptide Science》1997,4(4-6):447-454
The PPGMRPP sequence, found in several copies in the Sm and U1RNPautoantigens, is the main target of anti-Sm and anti-U1RNP antibodies insystemic lupus erythematosus (SLE) and mixed connective tissue disease(MCTD) patient's sera. It is also recognized, to a lower extent, byanti-Ro/SSA and anti-La/SSB specificities. The PPGMRPP-NH2peptide amide and the PPGMRPP peptide, which is bound to a pentamericsequential oligopeptide carrier (SOC5), were examined by1H-NMR spectroscopy and ELISA assays, using sera from patientswith autoimmune rheumatic diseases. Among the three main conformers foundfor the free PPGMRPP, the extended one was also identified for PPGMRPP-NH2 and (PPGMRPP)5-SOC5.This can be attributed to the absence of ionic interactions between theArg-guanidinium and the carboxylate group in the amide andSOC5-bound forms of the peptide. Immunoassays using sera fromvarious specificities showed an enhanced anti-Sm and anti-U1RNP recognitionof PPGMRPP-NH2 and(PPGMRPP)5-SOC5, and lowering of the anti-Ro/SSAand anti-La/SSB reactivity. The presence of multiple conformers of freePPGMRPP may explain the unexpected cross-reactivity to the anti-Ro/Lapositive sera, while the prevalence of the extended conformation inPPGMRPP-NH2 and (PPGMRPP)5-SOC5is mainly responsible for the enhanced recognition from the anti-Sm andanti-U1RNP autoantibodies. It is concluded that the antigenic specificity ofPPGMRPP-NH2 and (PPGMRPP)5-SOC5 ismainly induced by conformational changes resulting from the conversion ofthe C-terminal carboxylate group to the amide form. 相似文献
976.
The counterreceptor binding site of human CD2 exhibits an extended surface patch with multiple conformations fluctuating with millisecond to microsecond motions. 总被引:3,自引:1,他引:2 下载免费PDF全文
D. F. Wyss K. T. Dayie G. Wagner 《Protein science : a publication of the Protein Society》1997,6(3):534-542
We have used 15N NMR relaxation experiments to probe, for the glycosylated human CD2 adhesion domain, the overall molecular motion, as well as very fast nanosecond-picosecond (ns-ps) and slow millisecond-microsecond (ms-microsecond) internal motions. Using a novel analysis method that considers all residues, we obtained a correlation time for the overall motion of 9.5 +/- 0.3 ns. Surprisingly, we found a large contiguous patch of residues in the counterreceptor (CD58) binding site of human CD2 exhibiting slow conformational exchange motions (ms-microsecond). On the other hand, almost none of the residues of the CD58 binding side display fast (ns-ps) internal motions of amplitudes larger than what is seen for well-ordered regions of the structure. Residues close to the N-glycosylation site, and the first N-acetylglucosamine of the high mannose glycan are as rigid as the protein core. Residues conserved in the immunoglobulin superfamily V-set domain are generally very rigid. 相似文献
977.
978.
Validation of the Greater Hunter Native Vegetation Mapping as it pertains to the Upper Hunter region of New South Wales 下载免费PDF全文
John T. Hunter 《Ecological Management & Restoration》2016,17(1):40-46
Reliable vegetation maps are an important component of any long‐term landscape planning initiatives. A number of approaches are available but one, in particular, pattern recognition (segmentation) combined with modelling from floristic site data, is currently being used to map vegetation across NSW. An independent assessment of this approach based on a review of the Greater Hunter Native Vegetation Mapping (GHM_v4) was undertaken in order to assess its ability to cater for regional, local, strategic and landscape planning. The validation process tested 2151 locations across the Upper Hunter Valley region of New South Wales (NSW), Australia. The results suggest that mapping at the coarsest level of NSW vegetation classification, the Formation, is generally poor, with only Dry Sclerophyll Forest and Woodland modelled with some level of reliability. The modelled mapping of individual plant community types (PCTs) was found to be highly inaccurate with only 17% of validation points attributed as ‘correct’ and a further 13% ‘essentially correct’. Therefore, a majority of PCTs were mapped with an accuracy of less than 30%. The results of this validation suggest that the GHM_v4 is of such a low level of accuracy within the upper Hunter as to be inherently unusable for broad‐scale regional and local landscape planning or environmental assessment, including locating compensatory offsets for the loss of native vegetation due to developments. The GHM_v4 methods of pattern recognition of mainly SPOT5 satellite imagery combined with modelling from plot data have not produced reliable vegetation maps of plant community types. Yet this mapping programme is extending across NSW and could be misused for environmental decisions or as a regulation. 相似文献
979.
Structural analysis of nested neutralizing and non‐neutralizing B cell epitopes on ricin toxin's enzymatic subunit 下载免费PDF全文
Michael J. Rudolph David J. Vance Michael S. Cassidy Yinghui Rong Charles B. Shoemaker Nicholas J. Mantis 《Proteins》2016,84(8):1162-1172
In this report, we describe the X‐ray crystal structures of two single domain camelid antibodies (VHH), F5 and F8, each in complex with ricin toxin's enzymatic subunit (RTA). F5 has potent toxin‐neutralizing activity, while F8 has weak neutralizing activity. F5 buried a total of 1760 Å2 in complex with RTA and made contact with three prominent secondary structural elements: α‐helix B (Residues 98–106), β‐strand h (Residues 113–117), and the C‐terminus of α‐helix D (Residues 154–156). F8 buried 1103 Å2 in complex with RTA that was centered primarily on β‐strand h. As such, the structural epitope of F8 is essentially nested within that of F5. All three of the F5 complementarity determining regions CDRs were involved in RTA contact, whereas F8 interactions were almost entirely mediated by CDR3, which essentially formed a seventh β‐strand within RTA's centrally located β‐sheet. A comparison of the two structures reported here to several previously reported (RTA‐VHH) structures identifies putative contact sites on RTA, particularly α‐helix B, associated with potent toxin‐neutralizing activity. This information has implications for rational design of RTA‐based subunit vaccines for biodefense. Proteins 2016; 84:1162–1172. © 2016 Wiley Periodicals, Inc. 相似文献
980.
Transcriptome‐based profiling of yolk sac‐derived macrophages reveals a role for Irf8 in macrophage maturation 下载免费PDF全文