Hydration of "Nonfouling" Functional Groups

被引:82
作者
Hower, Jason C. [1 ]
Bernards, Matthew T. [1 ]
Chen, Shengfu [1 ]
Tsao, Heng-Kwong [2 ]
Sheng, Yu-Jane [3 ]
Jiang, Shaoyi [1 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Natl Cent Univ, Dept Chem Engn, Chungli 320, Taiwan
[3] Natl Taiwan Univ, Dept Chem Engn, Taipei 106, Taiwan
基金
美国国家科学基金会;
关键词
SELF-ASSEMBLED MONOLAYERS; APPARENT MOLAL VOLUMES; PROTEIN ADSORPTION; ADIABATIC COMPRESSIBILITIES; MOLECULAR SIMULATION; SURFACE INTERACTIONS; AMINO-ACIDS; DYNAMICS; WATER; 25-DEGREES-C;
D O I
10.1021/jp8065713
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The prevention of nonspecific protein adsorption to synthetic materials and devices presents a major design challenge in the biomedical community. While some chemical groups can resist nonspecific protein adsorption from simple solutions for limited contact times, there remains a need for new nonfouling functional groups and surface coatings that prevent protein adsorption from complex media like blood or in harsh environments like seawater. Recent studies of the molecular mechanisms of nonfouling surfaces have identified a strong correlation between surface hydration and resistance to nonspecific protein adsorption. In this work, we describe a simple experimental method for evaluating the intrinsic hydration capacity of model surface coating functional groups based on the partial molal volume at infinite dilution. In order to evaluate a range of hydration capacity and nonfouling performance, solutes were selected from three classes: ethylene glycols, sugar alcohols, and glycine analogues. The number of hydrating water molecules bound to a solute was estimated by comparing the molecular volume at infinite dilution to the Solute van der Waals molecular volume. The number of water molecules associated with each solute was further validated by constant pressure and temperature molecular dynamics simulations. Finally, a size-normalized molecular volume was correlated to previously observed protein adsorption experiments to relate the intrinsic hydration capacity of functional groups to their known nonfouling abilities.
引用
收藏
页码:197 / 201
页数:5
相关论文
共 40 条
[1]  
Allen Tildesley D.J., 1987, Computer Simulation of Liquids
[2]   Theory of hydration forces between surfaces [J].
Besseling, NAM .
LANGMUIR, 1997, 13 (07) :2113-2122
[3]   Surface functionalization for self-referencing surface plasmon resonance (SPR) biosensors by multi-step self-assembly [J].
Boozer, C ;
Yu, QM ;
Chen, SF ;
Lee, CY ;
Homola, J ;
Yee, SS ;
Jiang, SY .
SENSORS AND ACTUATORS B-CHEMICAL, 2003, 90 (1-3) :22-30
[4]   CHARMM - A PROGRAM FOR MACROMOLECULAR ENERGY, MINIMIZATION, AND DYNAMICS CALCULATIONS [J].
BROOKS, BR ;
BRUCCOLERI, RE ;
OLAFSON, BD ;
STATES, DJ ;
SWAMINATHAN, S ;
KARPLUS, M .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1983, 4 (02) :187-217
[5]   INFLUENCE OF BASE COMPOSITION, BASE SEQUENCE, AND DUPLEX STRUCTURE ON DNA HYDRATION - APPARENT MOLAR VOLUMES AND APPARENT MOLAR ADIABATIC COMPRESSIBILITIES OF SYNTHETIC AND NATURAL DNA DUPLEXES AT 25-DEGREES-C [J].
CHALIKIAN, TV ;
SARVAZYAN, AP ;
PLUM, GE ;
BRESLAUER, KJ .
BIOCHEMISTRY, 1994, 33 (09) :2394-2401
[6]   Surveying for surfaces that resist the adsorption of proteins [J].
Chapman, RG ;
Ostuni, E ;
Takayama, S ;
Holmlin, RE ;
Yan, L ;
Whitesides, GM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (34) :8303-8304
[7]   A new avenue to nonfouling materials [J].
Chen, Shengfu ;
Jiang, Shaoyi .
ADVANCED MATERIALS, 2008, 20 (02) :335-+
[8]   Strong resistance of a thin crystalline layer of balanced charged groups to protein adsorption [J].
Chen, Shengfu ;
Yu, Fuchen ;
Yu, Qiuming ;
He, Yi ;
Jiang, Shaoyi .
LANGMUIR, 2006, 22 (19) :8186-8191
[9]   APPARENT MOLAL VOLUMES AND ADIABATIC COMPRESSIBILITIES OF ETHYLENE-GLYCOL DERIVATIVES IN WATER AT 5-DEGREES-C, 25-DEGREES-C, AND 45-DEGREES-C [J].
HARADA, S ;
NAKAJIMA, T ;
KOMATSU, T ;
NAKAGAWA, T .
JOURNAL OF SOLUTION CHEMISTRY, 1978, 7 (06) :463-474
[10]  
HORBETT TA, 1982, ADV CHEM SER, V199, P233