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通过二维凝胶的计算机分析确定黑色素瘤分化过程中的蛋白质表达变化。

Changes in protein expression during melanoma differentiation determined by computer analysis of 2-D gels.

作者信息

Easty D, Hart I R, Patel K, Seymour C, Yacoub M, Domscheit A, Gunther S, Postel W, Gorg A, Dunn M J

机构信息

Imperial Cancer Research Fund, Lincoln's Inn Fields, London, U.K.

出版信息

Clin Exp Metastasis. 1991 May-Jun;9(3):221-30. doi: 10.1007/BF01753726.

Abstract

Cytodifferentiation in many melanocytic cells is regulated through the adenylate cyclase-cAMP pathway. To analyse the molecular changes associated with this process we have compared the proteins produced by two closely related cell lines which, though derived from a single cell line, respond very differently to modulation of this signalling pathway. The human melanoma cell line DX3 shows little change in in vitro characteristics following treatment with cAMP elevating agents; in contrast the more malignant DX3 LT5.1 variant, derived from the DX3 parental line, shows pronounced dendrification, decreased proliferation and a reduction in metastatic capacity after similar treatment. The two cell lines were treated with phosphodiesterase inhibitors for 5 days and then processed for two-dimensional gel characterization using an immobilized pH gradient for the IEF dimension. Proteins were detected by silver staining the gels and protein intensities were digitized using a laser densitometer. Two-dimensional gel patterns were edited, matched and a melanoma protein database of 637 spots constructed using PDQUEST software on an Orion 1/05 computer. Eleven proteins were lost and four new proteins were detected in both cell lines following treatment. Twenty-two proteins were present in DX3 LT5.1 after treatment but not in untreated lines or treated DX3. These differentially expressed proteins may be associated with the observed changes in differentiation patterns and metastasis. Our results illustrate the resolving power of this technique and suggest potential applications to the study of cellular differentiation.

摘要

许多黑素细胞中的细胞分化是通过腺苷酸环化酶 - cAMP途径来调节的。为了分析与此过程相关的分子变化,我们比较了两个密切相关的细胞系所产生的蛋白质,这两个细胞系虽然源自同一个细胞系,但对该信号通路的调节反应却非常不同。人黑色素瘤细胞系DX3在用提高cAMP的试剂处理后,其体外特性几乎没有变化;相反,源自DX3亲代系的恶性程度更高的DX3 LT5.1变体,在经过类似处理后,显示出明显的树突化、增殖减少和转移能力降低。将这两个细胞系用磷酸二酯酶抑制剂处理5天,然后使用固定化pH梯度进行等电聚焦(IEF)维度的二维凝胶表征。通过对凝胶进行银染来检测蛋白质,并使用激光密度计将蛋白质强度数字化。使用PDQUEST软件在Orion 1/05计算机上对二维凝胶图谱进行编辑、匹配,并构建了一个包含637个斑点的黑色素瘤蛋白质数据库。处理后,两个细胞系中均有11种蛋白质消失,4种新蛋白质被检测到。处理后的DX3 LT5.1中有22种蛋白质存在,但未处理的细胞系或处理后的DX3中没有。这些差异表达的蛋白质可能与观察到的分化模式和转移变化有关。我们的结果说明了该技术的分辨能力,并提示了其在细胞分化研究中的潜在应用。

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