Literature DB >> 10353705

A new concept in polytopic membrane proteins following from the study of band 3 protein.

N Hamasaki1, H Kuma, K Ota, M Sakaguchi, K Mihara.   

Abstract

In the present communication, we introduce a novel concept in multispanning polytopic membrane proteins revealed by the study of the band 3 protein. The transmembrane domain of such proteins can be divided into three categories, that is, hydrophilic loops connecting transmembrane peptides (category 1), portions embedded by peptide-peptide interactions (category 2), and portions embedded by peptide-lipid interactions (category 3). Category 2 peptides of polytopic membrane proteins were found to stably reside in the lipid bilayer without peptide-lipid interactions that had been thought to be essential for transmembrane segments. Category 3 peptides are equivalent to single-spanning segments of bitopic membrane proteins. Three different experiments, namely proteolytic digestion, chemical modification of the band 3 protein, and cell free transcription and translation, were used to categorize the transmembrane peptides.

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Year:  1998        PMID: 10353705     DOI: 10.1139/bcb-76-5-729

Source DB:  PubMed          Journal:  Biochem Cell Biol        ISSN: 0829-8211            Impact factor:   3.626


  3 in total

1.  The role of band 3 protein in oxygen delivery by red blood cells.

Authors:  N Hamasaki
Journal:  Indian J Clin Biochem       Date:  1999-01

2.  Topology of transmembrane segments 1-4 in the human chloride/bicarbonate anion exchanger 1 (AE1) by scanning N-glycosylation mutagenesis.

Authors:  Joanne C Cheung; Jing Li; Reinhart A F Reithmeier
Journal:  Biochem J       Date:  2005-08-15       Impact factor: 3.857

Review 3.  Cell physiology and molecular mechanism of anion transport by erythrocyte band 3/AE1.

Authors:  Michael L Jennings
Journal:  Am J Physiol Cell Physiol       Date:  2021-10-20       Impact factor: 4.249

  3 in total

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