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A New Protein-Protein Interaction Sensor Based on Tripartite Split-GFP Association

Scientific reports, 2013-10, Vol.3 (1), p.2854-2854, Article 2854

2013

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Engineering and characterization of a superfolder green fluorescent protein

Nature biotechnology, 2006-01, Vol.24 (1), p.79-88

2006

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Engineering an efficient and bright split Corynactis californica green fluorescent protein

Scientific reports, 2021-09, Vol.11 (1), p.18440-18440, Article 18440

2021

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Solution structure of the type I polyketide synthase Pks13 from Mycobacterium tuberculosis

BMC biology, 2022-06, Vol.20 (1), p.147-147, Article 147

2022

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Construction, characterization and crystal structure of a fluorescent single-chain Fv chimera

Protein engineering, design and selection, 2021-02, Vol.34

2021

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A Suite of Engineered GFP Molecules for Oligomeric Scaffolding

Structure (London), 2015-09, Vol.23 (9), p.1754-1768

2015

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Genetic screens and directed evolution for protein solubility

Current opinion in chemical biology, 2003-02, Vol.7 (1), p.33-38

Waldo, Geoffrey S

2003

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Selection and verification of antibodies against the cytoplasmic domain of M2 of influenza, a transmembrane protein

mAbs, 2020-01, Vol.12 (1), p.1843754-1843754

2020

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New molecular reporters for rapid protein folding assays

PloS one, 2008-06, Vol.3 (6), p.e2387-e2387

2008

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One-step split GFP staining for sensitive protein detection and localization in mammalian cells

BioTechniques, 2010-10, Vol.49 (4), p.727-736

2010

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Disulfide bonds within the C2 domain of RAGE play key roles in its dimerization and biogenesis

PloS one, 2012-12, Vol.7 (12), p.e50736

2012

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Split green fluorescent protein as a modular binding partner for protein crystallization

Acta crystallographica. Section D, Biological crystallography., 2013-12, Vol.69 (12), p.2513-2523

2013

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In vivo and in vitro protein solubility assays using split GFP

Nature methods, 2006-10, Vol.3 (10), p.845-854

2006

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Domain Orientation in the Inactive Response Regulator Mycobacterium tuberculosis MtrA Provides a Barrier to Activation

Biochemistry (Easton), 2007-06, Vol.46 (23), p.6733-6743

2007

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Subfamily-specific adaptations in the structures of two penicillin-binding proteins from Mycobacterium tuberculosis

PloS one, 2014-12, Vol.9 (12), p.e116249-e116249

2014

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Fluorescent labeling of antibody fragments using split GFP

PloS one, 2011-10, Vol.6 (10), p.e25727-e25727

2011

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Expression and use of superfolder green fluorescent protein at high temperatures in vivo: a tool to study extreme thermophile biology

Environmental microbiology, 2008-03, Vol.10 (3), p.605-613

2008

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Protein tagging and detection with engineered self-assembling fragments of green fluorescent protein

Nature biotechnology, 2005-01, Vol.23 (1), p.102-107

2005

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Engineering highly stable variants of Corynactis californica green fluorescent proteins

Protein science, 2024-02, Vol.33 (2), p.e4886-n/a

2024

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High-Throughput Protein-Protein Interaction Assays Using Tripartite Split-GFP Complementation

Methods in molecular biology (Clifton, N.J.), 2019, Vol.2025, p.423

2019

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High-Throughput Isolation of Soluble Protein Domains Using a Bipartite Split-GFP Complementation System

Methods in molecular biology (Clifton, N.J.), 2019, Vol.2025, p.321

2019

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Library methods for structural biology of challenging proteins and their complexes

Current opinion in structural biology, 2013-06, Vol.23 (3), p.403-408

2013

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Recent advances in GFP folding reporter and split-GFP solubility reporter technologies. Application to improving the folding and solubility of recalcitrant proteins from Mycobacterium tuberculosis

Journal of structural and functional genomics, 2005-09, Vol.6 (2-3), p.113-119

2005

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Rapid protein-folding assay using green fluorescent protein

Nature biotechnology, 1999-07, Vol.17 (7), p.691-695

1999

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The Brucella TIR-like protein TcpB interacts with the death domain of MyD88

Biochemical and biophysical research communications, 2012-01, Vol.417 (1), p.299-304

2012

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A New Protein-Protein Interaction Sensor Based on Tripartite Split-GFP Association

Engineering and characterization of a superfolder green fluorescent protein

Engineering an efficient and bright split Corynactis californica green fluorescent protein

Solution structure of the type I polyketide synthase Pks13 from Mycobacterium tuberculosis

Construction, characterization and crystal structure of a fluorescent single-chain Fv chimera

A Suite of Engineered GFP Molecules for Oligomeric Scaffolding

Genetic screens and directed evolution for protein solubility

Selection and verification of antibodies against the cytoplasmic domain of M2 of influenza, a transmembrane protein

New molecular reporters for rapid protein folding assays

One-step split GFP staining for sensitive protein detection and localization in mammalian cells

Disulfide bonds within the C2 domain of RAGE play key roles in its dimerization and biogenesis

Split green fluorescent protein as a modular binding partner for protein crystallization

In vivo and in vitro protein solubility assays using split GFP

Domain Orientation in the Inactive Response Regulator Mycobacterium tuberculosis MtrA Provides a Barrier to Activation

Subfamily-specific adaptations in the structures of two penicillin-binding proteins from Mycobacterium tuberculosis

Fluorescent labeling of antibody fragments using split GFP

Expression and use of superfolder green fluorescent protein at high temperatures in vivo: a tool to study extreme thermophile biology

Protein tagging and detection with engineered self-assembling fragments of green fluorescent protein

Engineering highly stable variants of Corynactis californica green fluorescent proteins

High-Throughput Protein-Protein Interaction Assays Using Tripartite Split-GFP Complementation

High-Throughput Isolation of Soluble Protein Domains Using a Bipartite Split-GFP Complementation System

Library methods for structural biology of challenging proteins and their complexes

Recent advances in GFP folding reporter and split-GFP solubility reporter technologies. Application to improving the folding and solubility of recalcitrant proteins from Mycobacterium tuberculosis

Rapid protein-folding assay using green fluorescent protein

The Brucella TIR-like protein TcpB interacts with the death domain of MyD88

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