Polyanions and the proteome

被引:93
作者
Jones, LS [1 ]
Yazzie, B [1 ]
Middaugh, CR [1 ]
机构
[1] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66047 USA
关键词
D O I
10.1074/mcp.R400008-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The behavior of the proteome reflects spatial and temporal organization both within and without cells. We propose that various macromolecular entities possessing polyanionic character such as proteoglycans, lipid bilayer surfaces, microtubules, microfilaments, and polynucleotides may provide a functional network that mediates a variety of cellular phenomena. The interaction of proteins with this array of polyanions is characterized by a lower degree of specificity than seen with most commonly recognized macromolecular interactions. In this commentary, potential roles for this polyanion network in diverse functions such as protein/protein interactions, protein folding and stabilization, macromolecular transport, and various disease processes are all considered, as well as the use of polyanions as therapeutic agents. The role of small polyanions in the regulation of protein/polyanion interactions is also postulated. We provide preliminary experimental analysis of the extent to which proteins interact with polyanions inside cells using a combination of two-dimensional chromatographic and electrophoretic methods and antibody arrays. We conclude that many hundreds to thousands of such interactions are present in cells and argue that future understanding of the proteome will require that the "polyanion world" be taken into account.
引用
收藏
页码:746 / 769
页数:24
相关论文
共 173 条
[81]   Amyloid-specific heparan sulfate from human liver and spleen [J].
Lindahl, B ;
Lindahl, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26091-26094
[82]   Aberrant glycosylation modulates phosphorylation of tau by protein kinase A and dephosphorylation of tau by protein phosphatase 2A and 5 [J].
Liu, F ;
Zaidi, T ;
Iqbal, K ;
Grundke-Iqbal, I ;
Gong, CX .
NEUROSCIENCE, 2002, 115 (03) :829-837
[83]  
LUST G, 1992, AM J VET RES, V53, P1836
[84]   INTERACTION OF PARTIALLY STRUCTURED STATES OF ACIDIC FIBROBLAST GROWTH-FACTOR WITH PHOSPHOLIPID-MEMBRANES [J].
MACH, H ;
MIDDAUGH, CR .
BIOCHEMISTRY, 1995, 34 (31) :9913-9920
[85]   NATURE OF THE INTERACTION OF HEPARIN WITH ACIDIC FIBROBLAST GROWTH-FACTOR [J].
MACH, H ;
VOLKIN, DB ;
BURKE, CJ ;
MIDDAUGH, CR ;
LINHARDT, RJ ;
FROMM, JR ;
LOGANATHAN, D ;
MATTSSON, L .
BIOCHEMISTRY, 1993, 32 (20) :5480-5489
[86]   PARTIALLY STRUCTURED SELF-ASSOCIATING STATES OF ACIDIC FIBROBLAST GROWTH-FACTOR [J].
MACH, H ;
RYAN, JA ;
BURKE, CJ ;
VOLKIN, DB ;
MIDDAUGH, CR .
BIOCHEMISTRY, 1993, 32 (30) :7703-7711
[87]   PROBING THE AFFINITY OF POLYANIONS FOR ACIDIC FIBROBLAST GROWTH-FACTOR BY UNFOLDING KINETICS [J].
MACH, H ;
MIDDAUGH, CR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 309 (01) :36-42
[88]   Evidence for two distinct binding sites for tau on microtubules [J].
Makrides, V ;
Massie, MR ;
Feinstein, SC ;
Lew, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) :6746-6751
[89]   Chaperone-like activity of tubulin - Binding and reactivation of unfolded substrate enzymes [J].
Manna, T ;
Sarkar, T ;
Poddar, A ;
Roychowdhury, M ;
Das, KP ;
Bhattacharyya, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (43) :39742-39747
[90]   Specificity and stability in topology of protein networks [J].
Maslov, S ;
Sneppen, K .
SCIENCE, 2002, 296 (5569) :910-913