NMR studies of BPTI aggregation by using paramagnetic relaxation reagents

被引:13
作者
Bernini, Andrea
Spiga, Ottavia
Clutti, Arianna
Venditti, Vincenzo
Prischi, Filippo
Governatori, Mariangela
Bracci, Luisa
Lelli, Barbara
Pileri, Silvia
Botta, Mauro
Barge, Alessandro
Laschi, Franco
Niccolai, Neri
机构
[1] Univ Siena, Biomol Struct Res Ctr, I-53100 Siena, Italy
[2] Univ Siena, Dipartimento Biol Mol, I-53100 Siena, Italy
[3] SienaBioGrafiX Srl, I-53100 Siena, Italy
[4] Univ Piemonte Orientale, Dipartimento Sci & Tecnol Avanzate, I-15100 Alessandria, Italy
[5] Univ Siena, Dipartimento Chim, I-53100 Siena, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2006年 / 1764卷 / 05期
关键词
NMR; paramagnetic probe; TEMPOL; surface accessibility; Gd(III)DTPA-BMA; protein aggregation; BPTI;
D O I
10.1016/j.bbapap.2006.02.013
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
Paramagnetic probes, whose approach to proteins can be monitored by nuclear magnetic resonance (NMR) studies, have been found of primary relevance for investigating protein surfaces accessibility. Here, paramagnetic probes are also suggested for a systematic investigation on protein aggregation. Bovin pancreatic trypsin inhibitor (BPTI) was used as a model system for aggregation by analyzing its interaction with TEMPOL and Gd(III)DTPA-BMA. Some of the measured paramagnetic relaxation rates of BPTI protons exhibited a reverse dependence on protein concentration, which can be attributed to the formation of transient BPTI aggregates. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:856 / 862
页数:7
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