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1.
All plant cells are provided with the necessary rigidity to withstand the turgor by an exterior cell wall. This wall is composed
of long crystalline cellulose microfibrils embedded in a matrix of other polysaccharides. The cellulose microfibrils are deposited
by mobile membrane bound protein complexes in remarkably ordered lamellar textures. The mechanism by which these ordered textures
arise, however, is still under debate. The geometrical model for cell wall deposition proposed by Emons and Mulder (Proc.
Natl. Acad. Sci. 95, 7215–7219, 1998) provides a detailed approach to the case of cell wall deposition in non-growing cells, where there is no evidence for the
direct influence of other cellular components such as microtubules. The model successfully reproduces even the so-called helicoidal
wall; the most intricate texture observed. However, a number of simplifying assumptions were made in the original calculations.
The present work addresses the issue of the robustness of the model to relaxation of these assumptions, by considering whether
the helicoidal solutions survive when three aspects of the model are varied. These are: (i) the shape of the insertion domain,
(ii) the distribution of lifetimes of individual CSCs, and (iii) fluctuations and overcrowding. Although details of the solutions
do change, we find that in all cases the overall character of the helicoidal solutions is preserved. 相似文献
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Pinkerton K. E.; Lewis J.; Mulder A. M.; Ikegami M.; Jobe A. H. 《Journal of applied physiology》1993,74(3):1240-1247
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Nataly Mancette Rijensky Netta R. Blondheim Shraga Eilon Barnea Nir Peled Eli Rosenbaum Aron Popovtzer Solomon M. Stemmer Alejandro Livoff Mark Shlapobersky Neta Moskovits Dafna Perry Eitan Rubin Itzhak Haviv Arie Admon 《Molecular & cellular proteomics : MCP》2020,19(8):1360-1374
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- •Sufficient tumor tissues are often unavailable large HLA peptidome discovery.
- •Using patient derived xenograft (PDX) tumors can overcome this limitation.
- •The large PDX HLA peptidomes expand significantly those of the original biopsies.
- •The HLA peptidomes of the PDX tumors included many tumor antigens.
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Chris J. van Koppen Marcel W. Hermanussen Kiek N. Verrijp Jaap F. Rodrigues de Miranda Arie J. Beld Jan-Willem J. Lammers Cees A. M. van Ginneken 《Life sciences》1987,40(26):2561-2570
Specific binding of [125I]-(−)-cyanopindolol to human tracheal smooth muscle membranes was saturable, stereo-selective and of high affinity (Kd=5.3±0.9 pmol/l and RT=78±7fmol/g tissue). The β1-selective antagonists atenolol and LK 203-030 inhibited specific [125I]-(−)-cyanopindolol binding according to a one binding site model with low affinity in nearly all subjects, pointing to a homogeneous β2-adrenoceptor population. In one subject using LK 203-030 a small β-adrenoceptor subpopulation could be demonstrated. The beta-mimetics isoprenaline, fenoterol, salbutamol and terbutaline recognized high and low affinity agonist binding sites. Isoprenaline's pKH- and pKL- values for the high and low affinity sites were 8.0±0.2 and 5.9±0.3 respectively. In functional experiments isoprenaline relaxed tracheal smooth muscle strips having intrinsic tone with a pD2-value of 6.63±0.19. 相似文献