Useful Tools for Biomolecule Isolation, Detection, and Identification: Acylhydrazone-Based Cleavable Linkers

被引:65
作者
Park, Ki Duk [1 ]
Liu, Rihe [1 ,2 ]
Kohn, Harold [1 ,3 ]
机构
[1] Univ N Carolina, Eshelman Sch Pharm, Div Med Chem & Nat Prod, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Carolina Ctr Genome Sci, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
来源
CHEMISTRY & BIOLOGY | 2009年 / 16卷 / 07期
关键词
BIOTIN-BINDING; STREPTAVIDIN INTERACTION; AFFINITY-CHROMATOGRAPHY; NUCLEOPHILIC CATALYSIS; AVIDIN; PROTEINS; IMMOBILIZATION; PURIFICATION; NUCLEOTIDE; STABILITY;
D O I
10.1016/j.chembiol.2009.06.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteomic searches using affinity-based chromatography (e.g., biotin-[strept]avidin) have been severely hampered by low protein recovery yields, protein destruction and denaturation, and the release of background proteins from the support. These limitations confound protein identification. A new acylhydrazone-based cleavable linker was developed to permit the efficient isolation of proteins with a traceable tag allowing detection and identification under mild conditions. The utility of the acylhydrazone linker was validated in a proteomic search wherein aldehyde dehydrogenase-1 was selectively captured and isolated from the mouse soluble liver proteome without interfering background proteins. The use of acylhydrazone linkers is expected to be generalized, allowing for the selective release of tagged molecules from noncovalent and covalently tagged supports.
引用
收藏
页码:763 / 772
页数:10
相关论文
共 52 条
[41]   NMR study of conformation and isomerization of aryl- and heteroarylaldehyde 4-tert-butylphenoxyacetylhydrazones [J].
Syakaev, Victor V. ;
Podyachev, Sergey N. ;
Buzykin, Boris I. ;
Latypov, Shamil K. ;
Habicher, Wolf D. ;
Konovalov, Alexander I. .
JOURNAL OF MOLECULAR STRUCTURE, 2006, 788 (1-3) :55-62
[42]   PHOTOCLEAVABLE BIOTINYLATED LIGANDS FOR AFFINITY-CHROMATOGRAPHY [J].
THIELE, C ;
FAHRENHOLZ, F .
ANALYTICAL BIOCHEMISTRY, 1994, 218 (02) :330-337
[43]   SOLID-PHASE METHOD FOR THE PURIFICATION OF DNA SEQUENCING REACTIONS [J].
TONG, XC ;
SMITH, LM .
ANALYTICAL CHEMISTRY, 1992, 64 (22) :2672-2677
[44]   Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides [J].
Tornoe, CW ;
Christensen, C ;
Meldal, M .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (09) :3057-3064
[45]   Development of a novel chemical probe for the selective enrichment of phosphorylated serine- and threonine-containing peptides [J].
van der Veken, P ;
Dirksen, EHC ;
Ruijter, E ;
Elgersma, RC ;
Heck, AJR ;
Rijkers, DTS ;
Slijper, M ;
Liskamp, RMJ .
CHEMBIOCHEM, 2005, 6 (12) :2271-2280
[46]   A mild chemically cleavable linker system for functional proteomic applications [J].
Verhelst, Steven H. L. ;
Fonovic, Marko ;
Bogyo, Matthew .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (08) :1284-1286
[47]   Chemical genetics [J].
Walsh, Daniel P. ;
Chang, Young-Tae .
CHEMICAL REVIEWS, 2006, 106 (06) :2476-2530
[48]   Reaction of aldehydes and pyrazolones in the presence of sodium dodecyl sulfate in aqueous media [J].
Wang, W ;
Wang, SX ;
Qin, XY ;
Li, JT .
SYNTHETIC COMMUNICATIONS, 2005, 35 (09) :1263-1269
[49]   Disparate proteome reactivity profiles of carbon electrophiles [J].
Weerapana, Eranthie ;
Simon, Gabriel M. ;
Cravatt, Benjamin F. .
NATURE CHEMICAL BIOLOGY, 2008, 4 (07) :405-407
[50]  
WILCHEK M, 1990, METHOD ENZYMOL, V184, P14