Advances of the technologies in large-scale membrane proteome identification
Received date: 2019-09-08
Revised date: 2019-09-14
Online published: 2019-09-16
Supported by
Supported by the National Natural Science Foundation of China No(31670234)
Membrane proteins play important functions not only as receptors and transporters, but also in many other important intracellular functions such as photosynthetic and respiratory electron transport. Identification of membrane proteins is a necessary step to understand their functions. Membrane proteins are generally highly hydrophobic and difficult to be resolved by aqueous solutions, and large-scale proteomic identification of membrane proteins has been a great technical challenge. Significant efforts have been invested in the field to improve the solubility of membrane proteins in aqueous solutions that are compatible for mass spectrometry analysis. This review summarizes the main technological achievements in the field of membrane proteomics particularly for the improvement of membrane protein identification, and uses the photosynthetic model cyanobacterium Synechocystis sp. PCC6803 as an example to illustrate how technology advances push forward the field in terms of the increased coverage of membrane proteome identification.
Key words: membrane protein; proteomics; hydrophobicity; cyanobacterium
Dandan Lv,Yuanya Zhang,Haitao Ge,Xiahe Huang,Yingchun Wang . Advances of the technologies in large-scale membrane proteome identification[J]. Hereditas(Beijing), 2019 , 41(9) : 863 -874 . DOI: 10.16288/j.yczz.19-275
| [1] | Paulsen IT, Sliwinski MK, Nelissen B, Goffeau A, Saier MH Jr . Unified inventory of established and putative transporters encoded within the complete genome of Saccharomyces cerevisiae. FEBS Lett, 1998,430(1-2):116-125. | |||
| [2] | Wallin E, von Heijne G . Genome-wide analysis of integral membrane proteins from eubacterial, archaean, and eukaryotic organisms. Protein Sci, 1998,7(4):1029-1038. | |||
| [3] | Persson B, Argos P . Prediction of transmembrane segments in proteins utilising multiple sequence alignments. J Mol Biol, 1994,237(2):182-192. | |||
| [4] | Persson B, Argos P . Prediction of membrane protein topology utilizing multiple sequence alignments. J Protein Chem, 1997,16(5):453-457. | |||
| [5] | Brown DA, London E . Functions of lipid rafts in biological membranes. Annu Rev Cell Dev Biol, 1998,14:111-136. | |||
| [6] | Harder T, Simons K. Caveolae , DIGs, the dynamics of sphingolipid-cholesterol microdomains. Curr Opin Cell Biol, 1997,9(4):534-542. | |||
| [7] | Krogh A, Larsson B, von Heijne G, Sonnhammer , ELL . Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol, 2001,305(3):567-580. | |||
| [8] | Kyte J, Doolittle RF . A simple method for displaying the hydropathic character of a protein. J Mol Biol, 1982,157(1):105-132. | |||
| [9] | Erde J, Loo RR, Loo JA. Enhanced FASP (eFASP) to increase proteome coverage and sample recovery for quantitative proteomic experiments. J Proteome Res, 2014,13(4):1885-1895. | |||
| [10] | Fujiki Y, Hubbard AL, Fowler S, Lazarow PB . Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum. J Cell Biol, 1982,93(1):97-102. | |||
| [11] | Kieselbach T, Hagman, Andersson B, Schr?Der WP. The thylakoid lumen of chloroplasts. Isolation and characterization. J Bio Chem, 1998,273(12):6710-6716. | |||
| [12] | Liebler DC, Ham AJ . Spin filter-based sample preparation for shotgun proteomics. Nat Methods, 2009,6(11):785-786. | |||
| [13] | Ma F, Liu F, Xu W, Li L . Surfactant and chaotropic agent assisted sequential extraction/on-pellet digestion (SCAD) for enhanced proteomics. J Proteome Res, 2018,17(8):2744-2754. | |||
| [14] | Wu CC, Maccoss MJ, Howell KE, Yates JR . A method for the comprehensive proteomic analysis of membrane proteins. Nat Biotechnol, 2003,21(5):532-538. | |||
| [15] | Yu Y, Bekele S, Pieper R . Quick 96FASP for high throughput quantitative proteome analysis. J Proteomics, 2017,166:1-7. | |||
| [16] | Gao L, Ge H, Huang X, Liu K, Zhang Y, Xu W, Wang Y . System
/
|