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棘阿米巴吞噬溶酶体的体外融合。II 通过改进的电子显微镜和新的光学显微镜技术对体外液泡融合进行定量表征。

In vitro fusion of Acanthamoeba phagolysosomes. II Quantitative characterization of in vitro vacuole fusion by improved electron microscope and new light microscope techniques.

作者信息

Oates P J, Touster O

出版信息

J Cell Biol. 1978 Oct;79(1):217-34. doi: 10.1083/jcb.79.1.217.

Abstract

To investigate the properties of phagolysosome (PL) fusion in Acanthamoeba homogenates, it was necessary to develop reliable methods for measuring in vitro PL fusion. The need to distinguish PL fusion from PL adhesion was met by the development of a quantitative electron microscope assay. Initial characterization of the fusion reaction by this method was followed by the development of a more rapid light microscope assay. Results obtained by the two methods were found to be in close agreement. By use of these new techniques, the in vitro PL fusion reaction was demonstrated to occur in a quantitatively reproducible manner. Under the present conditions employed, PL breakdown was not detected at any time during the in vitro incubation, while PL fusion was observed to proceed linearly for approximately 10 min, at which time the reaction ceased. Incubation of mixtures of two distinct PL types resulted in increases in hybrid PL types that were paralleled by decreases in nonhybrid PL types. The relative changes in PL concentrations observed were quantitatively consistent with PL fusion occurring randomly with respect to PL type. PL fusion was strongly inhibited by low concentrations of KF (50% inhibition at 2.7 mM), and by approximately tenfold higher concentrations of KCl, while KCN and 2,4-dinitrophenol (2,4-DNP) had little effect. In addition to further defining the nature of the PL fusion reaction in this system, these results demonstrate that, by use of the techniques described, quantitative study of the biochemical properties of this reaction is now possible.

摘要

为了研究棘阿米巴匀浆中吞噬溶酶体(PL)融合的特性,有必要开发可靠的体外PL融合测量方法。通过开发一种定量电子显微镜检测方法,满足了区分PL融合与PL黏附的需求。在通过该方法对融合反应进行初步表征之后,又开发了一种更快的光学显微镜检测方法。发现这两种方法获得的结果非常一致。通过使用这些新技术,证明体外PL融合反应以定量可重复的方式发生。在目前采用的条件下,体外孵育过程中任何时候都未检测到PL分解,而观察到PL融合线性进行约10分钟,此时反应停止。两种不同PL类型的混合物孵育导致杂交PL类型增加,同时非杂交PL类型减少。观察到的PL浓度的相对变化在数量上与PL类型随机发生的PL融合一致。低浓度KF(2.7 mM时50%抑制)和大约高十倍浓度的KCl强烈抑制PL融合,而KCN和2,4-二硝基苯酚(2,4-DNP)影响很小。除了进一步确定该系统中PL融合反应的性质外,这些结果还表明,通过使用所述技术,现在可以对该反应的生化特性进行定量研究。

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Transmembrane flux of K42 in Acanthamoeba sp.棘阿米巴属中K42的跨膜通量
J Cell Comp Physiol. 1959 Apr;53:241-58. doi: 10.1002/jcp.1030530207.
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Improvements in epoxy resin embedding methods.环氧树脂包埋方法的改进。
J Biophys Biochem Cytol. 1961 Feb;9(2):409-14. doi: 10.1083/jcb.9.2.409.
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Membrane fusion.膜融合
Biochim Biophys Acta. 1973 Dec 28;300(4):421-65. doi: 10.1016/0304-4157(73)90015-4.

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