Platinization: A novel technique to anchor photosystem I reaction centres onto a metal surface at biological temperature and pH

被引:20
作者
Lee, JW [1 ]
Lee, I [1 ]
Greenbaum, E [1 ]
机构
[1] OAK RIDGE NATL LAB,OAK RIDGE,TN 37831
关键词
platinum; photosynthesis; PSI-metal binding; STM; tunnelling I-IV; welding;
D O I
10.1016/0956-5663(96)82733-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Photosystem I (PSI) reaction centre core antenna complexes containing about 40 chlorophylls per P700 (PSI-40) are 6 nm biological photovoltaic devices. PSI particles carry positively-charged domain(s) and can therefore interact electrostatically with a negatively-charged surface. PSI particles were platinized by reduction of [PtCl6](-2) at neutral pH and 20 degrees C. The presence of metallic platinum on PSI particles was observed directly by scanning tunnelling microscopy (STM). The platinized PSI particles were larger than control PSIs (without platinization), due to the presence of metallic platinum. The electric properties of PSI and metallic platinum were characterized by STM tunnelling conductance (I-V) measurements. Diodic response was obtained in platinized PSI. Metallic platinum formed during the reduction of [PtCl6](2-) caused bonding between PSI particles and a gold metal surface. Using the technique of chemical platinization, PSI particles can be ''welded'' onto gold plates under biologically compatible conditions, resulting in a 2-dimensional spatial array of PSI particles anchored on the metal surface. Metallic platinum is not only a good conductor but also an active catalyst. This platinization ''welding'' technique is potentially important for both bioelectronics and biometallocatalysis.
引用
收藏
页码:375 / 387
页数:13
相关论文
共 36 条
[21]   SCANNING TUNNELING SPECTROSCOPY OF METAL-SURFACES [J].
KUK, Y ;
SILVERMAN, PJ .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1990, 8 (01) :289-292
[22]   MOLECULAR ELECTRONICS OF A SINGLE PHOTOSYSTEM-I REACTION-CENTER - STUDIES WITH SCANNING-TUNNELING-MICROSCOPY AND SPECTROSCOPY [J].
LEE, I ;
LEE, JW ;
WARMACK, RJ ;
ALLISON, DP ;
GREENBAUM, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) :1965-1969
[23]  
LEE I, 1995, BIOPHYS J, V69, P652
[24]   QUENCHING OF CHLOROPHYLL EXCITED-STATES IN PHOTOSYSTEM-I BY QUINONES - STERN-VOLMER ANALYSIS OF FLUORESCENCE AND PHOTOCHEMICAL YIELD [J].
LEE, JW ;
ZIPFEL, W ;
OWENS, TG .
JOURNAL OF LUMINESCENCE, 1992, 51 (1-3) :79-89
[25]   PHOTOSYNTHETIC WATER-SPLITTING - IN-SITU PHOTOPRECIPITATION OF METALLOCATALYSTS FOR PHOTOEVOLUTION OF HYDROGEN AND OXYGEN [J].
LEE, JW ;
TEVAULT, CV ;
BLANKINSHIP, SL ;
COLLINS, RT ;
GREENBAUM, E .
ENERGY & FUELS, 1994, 8 (03) :770-773
[26]  
LEE JW, 1993, THESIS CORNELL U ITH
[27]   EFFECT OF DETERGENTS ON THE RELIABILITY OF A CHEMICAL-ASSAY FOR P-700 [J].
MARKWELL, JP ;
THORNBER, JP ;
SKRDLA, MP .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 591 (02) :391-399
[28]  
MOSBACH K, 1987, METHOD ENZYMOL, V135, P1
[29]   ANTENNA SIZE DEPENDENCE OF FLUORESCENCE DECAY IN THE CORE ANTENNA OF PHOTOSYSTEM-I - ESTIMATES OF CHARGE SEPARATION AND ENERGY-TRANSFER RATES [J].
OWENS, TG ;
WEBB, SP ;
METS, L ;
ALBERTE, RS ;
FLEMING, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (06) :1532-1536
[30]  
Rao K. K., 1992, P135