Factors governing electron capture by small disulfide loops in two-cysteine peptides

Journal of Physical Chemistry B

Volumn 112, Issue 43, 2008, Pages 13661-13669

  Dumont, Élise ^a   Loos, Pierre François ^a   Assfeld, Xavier ^a  

^a NANCY UNIVERSITÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; AMINO ACIDS; BINDING SITES; DIFFERENTIATION (CALCULUS); ELECTRON AFFINITY; ELECTRONS; HYDROGEN; MOLECULAR MODELING; MOLECULAR ORBITALS; ORGANIC ACIDS; PEPTIDES; PROTEINS;

CONSTRAINED STRUCTURES; ELECTRON CAPTURES; FACTORS CONTROLLING; INTRAMOLECULAR HYDROGEN BONDS; RADICAL ANIONS; REDOX ENZYMES; SHEDDING LIGHTS; STRUCTURAL DAMAGES; THIOREDOXIN; TURN STRUCTURES;

HYDROGEN BONDS;

EID: 55949129322     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp806465e     Document Type: Article

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89. 32,81 This would tend to suggest that our results are essentially transferable to condensed phases, as relative electron affinities will essentially remain constant. Thus we consider gas phase properties in this study.
90. 82
91. Another equivalent possibility is to report the number n′ of atoms of the arc: this measure is more suitable for comparison with organic compounds.
92. 32 systems presenting an horizontal stretching effect might result in a significant elongation.
93. 67 for an exhaustive description of experimental conditions. Let us note that these measurements involve complex reactions - a proton transfer occurs in a second step. The first step is likely to be kinetically determinant.
94. This would have the advantage to enable a discussion based on absolute electron affinities.
95. A hairpin corresponds to the association of two antiarallel β-sheets, linked solely by hydrogen bonds (Trpzip 4 is the most popular example).