Related references
Note: Only part of the references are listed.Picomolar affinity fibronectin domains engineered utilizing loop length diversity, recursive mutagenesis, and loop shuffling
Benjamin J. Hackel et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Simulation of Top7-CFr: A transient helix extension guides folding
Sandipan Mohanty et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
A tetrapeptide fragment -: based design method results in highly stable artificial proteins
Roman Dalluege et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2007)
Molecular dynamics simulations of the native and partially folded states of ubiquitin:: Influence of methanol cosolvent, pH, and temperature on the protein structure and dynamics
David B. Kony et al.
PROTEIN SCIENCE (2007)
Nonnatural protein-protein interaction-pair design by key residues grafting
Sen Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
The highly cooperative folding of small naturally occurring proteins is likely the result of natural selection
Alexander L. Watters et al.
CELL (2007)
Antibody constructs in cancer therapy - Protein engineering strategies to improve exposure in solid tumors
Robert A. Beckman et al.
CANCER (2007)
Antibody binding loop insertions as diversity elements
Csaba Kiss et al.
NUCLEIC ACIDS RESEARCH (2006)
Mis-translation of a computationally designed protein yields an exceptionally stable homodimer: Implications for protein engineering and evolution
Gautam Dantas et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Protein under pressure: Molecular dynamics simulation of the arc repressor
Daniel Trzesniak et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2006)
PIN-bodies:: A new class of antibody-like proteins with CD4 specificity derived from the protein inhibitor of neuronal nitric oxide synthase
C Bès et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Artificial, non-antibody binding proteins for pharmaceutical and industrial applications
T Hey et al.
TRENDS IN BIOTECHNOLOGY (2005)
Engineered antibody fragments and the rise of single domains
P Holliger et al.
NATURE BIOTECHNOLOGY (2005)
Binding proteins from alternative scaffolds
PÅ Nygren et al.
JOURNAL OF IMMUNOLOGICAL METHODS (2004)
Design of a novel globular protein fold with atomic-level accuracy
B Kuhlman et al.
SCIENCE (2003)
Novel therapies based on mechanisms of HIV-1 cell entry
JM Kilby et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)
Mapping the paratope of anti-CD4 recombinant fab 13B8.2 by combining parallel peptide synthesis and site-directed mutagenesis
C Bès et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
An affibody in complex with a target protein:: Structure and coupled folding
E Wahlberg et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Flow-cytometric isolation of human antibodies from a nonimmune Saccharomyces cerevisiae surface display library
MJ Feldhaus et al.
NATURE BIOTECHNOLOGY (2003)
Exploring the potential of the monobody scaffold: effects of loop elongation on the stability of a fibronectin type III domain
V Batori et al.
PROTEIN ENGINEERING (2002)
Evaluating conformational free energies: The colony energy and its application to the problem of loop prediction
ZX Xiang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Efficient CD4 binding and immunosuppressive properties of the 13B8.2 monoclonal antibody are displayed by its CDR-H1-derived peptide CB1
C Bès et al.
FEBS LETTERS (2001)
Topology, stability, sequence, and length: Defining the determinants of two-state protein folding kinetics
KW Plaxco et al.
BIOCHEMISTRY (2000)
NWChem: Exploiting parallelism in molecular simulations
TP Straatsma et al.
COMPUTER PHYSICS COMMUNICATIONS (2000)