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. 2008 Jul 2;295(3):C661–C678. doi: 10.1152/ajpcell.90650.2007

Table 5.

Proteins of which abundance in DRM fractions changed in response to dDAVP as quantified by LC-MS/MS

Protein Name; Gene Symbol Abundance in DRMs n P RefSeq Accession No.
Myosin 4; Myh4 1.0 ± 0.3 6 0.022 NP_062198.1
Keratin 15; Krt15 0.9 ± 0.3 4 0.064 NP_001004022.1
Keratin 19; Krt19 0.6 ± 0.2 6 0.042 NP_955792.1
Flotillin-2 (Reggie-1, REG-1); Flot2 0.4 ± 0.2 5 0.089 NP_114018.1
Keratin 12; Krt12 0.3 ± 0.1 10 0.022 NP_001008761.1
α-Actin cardiac; Actc1 0.3 ± 0.2 24 0.089 NP_062056.1
Keratin 75; Krt75 0.3 ± 0.1 35 0.038 NP_001008828.1
AQP1 (aquaporin-CHIP); AQP1 0.3 ± 0.1 3 0.025 NP_036910.1
Ras-related protein Rab7; Rab7 0.3 ± 0.1 3 0.055 NP_076440.1
Annexin A2; Anxa2 0.2 ± 0.1 24 0.066 NP_063970.1
Keratin 14; Krt14 0.2 ± 0.1 26 0.045 NP_001008751.1
β-Actin cytoplasmic; Actb −0.2 ± 0.1 12 0.033 NP_112406.1
Prohibitin; Phb −0.2 ± 0.1 5 0.059 NP_114039.1
Keratin 10; Krt10 −0.2 ± 0.1 58 0.023 NP_001008804.1
Annexin A1; Anxa1 −0.3 ± 0.1 6 0.001 NP_037036.1

Values are means ± SE, expressed as log2 relative peptide abundance identified in DRM fractions (fractions 4-6) of vehicle- and dDAVP-treated IMCD cells; n, number of peptide elution profiles. P values are results of t-test to determine whether a given protein identification showed an increase or a decrease in association with the DRM fraction after dDAVP treatment. Several proteins did not show significant changes: AQP2, ATP synthase mitochondrial F1 complex α-subunit, ATP synthase mitochondrial F1 complex β-subunit, ATPase V1 complex B2 subunit, ATPase H+-transporting V0 complex subunit d1, ATPase Na+-K+-transporting α1-subunit, B-cell receptor-associated protein 37, crystallin αB, cytochrome c oxidase subunit IV isoform 1, cytochrome c oxidase subunit Va, heat shock-related 70-kDa protein 2, keratin 4, keratin 8, vesicle-associated membrane protein 2, syntaxin 7, and similar to SPFH domain family member 2. LC-MS/MS, tandem mass spectrometry.