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Titlebook: Membrane Proteomics; Methods and Protocol Matthew J. Peirce,Robin Wait Book 2009 Humana Press 2009 Hydrophobicity.In silico.Lipid.Mammalian

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書目名稱Membrane Proteomics
副標(biāo)題Methods and Protocol
編輯Matthew J. Peirce,Robin Wait
視頻videohttp://file.papertrans.cn/631/630390/630390.mp4
概述Collects together in one volume the diverse practical approaches to analyzing membrane proteins.Includes both wet lab and in silico approaches.Includes protocols for the isolation of plasma membrane a
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Membrane Proteomics; Methods and Protocol Matthew J. Peirce,Robin Wait Book 2009 Humana Press 2009 Hydrophobicity.In silico.Lipid.Mammalian
描述The membranes surrounding cells and organelles constitute their interface with the local environment. The functions of membrane proteins include cell/cell and cell/extracellular matrix recognition, the reception and transduction of extracellular signals, and the tra- port of proteins, solutes and water molecules. Abnormal membrane protein expression has profound biological effects and may, for example, underlie phenotypic and functional differences between normal and tumour cells. Moreover the accessibility, particularly of plasma proteins traversing the plasma membrane of cells, makes them of particular ut- ity to the therapeutic intervention in disease. Indeed, it is estimated that of all currently licensed pharmaceuticals, approximately 70% target proteins resident in the plasma m- brane. In theory, unbiased technologies such as proteomics have the power to de?ne patterns of membrane protein expression characteristic of distinct states of cellular development, differentiation or disease, and thereby identify novel markers of, or targets for intervention in, disease. However, although about 25% of open reading frames in fully sequenced genomes are estimated to encode integral mem
出版日期Book 2009
關(guān)鍵詞Hydrophobicity; In silico; Lipid; Mammalian membrane proteins; Plant membrane proteins; Plasma and nuclea
版次1
doihttps://doi.org/10.1007/978-1-60327-310-7
isbn_softcover978-1-61737-889-8
isbn_ebook978-1-60327-310-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2009
The information of publication is updating

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Book 2009protein expression characteristic of distinct states of cellular development, differentiation or disease, and thereby identify novel markers of, or targets for intervention in, disease. However, although about 25% of open reading frames in fully sequenced genomes are estimated to encode integral mem
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Identification of Novel G Protein Coupled Receptorsmately 50% of marketed drugs are targeted toward a GPCR. Despite showing a high degree of structural homology, there is a large variance in sequence within the GPCR superfamily which has lead to difficulties in identifying and classifying potential new GPCR proteins. Here the various computational t
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Transcriptome-Based Identification of Candidate Membrane Proteinstic examination of the mammalian cell surfaces at the protein level is hampered by technical difficulties associated with proteomic analysis of so many membrane proteins and the large amounts of starting material required. The use of transcriptomic analyses avoids challenges associated with protein
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https://doi.org/10.1007/978-1-60327-310-7Hydrophobicity; In silico; Lipid; Mammalian membrane proteins; Plant membrane proteins; Plasma and nuclea
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