M. Hattarki

发表

Isolation of the new antigen receptor from wobbegong sharks, and use as a scaffold for the display of protein loop libraries.

P. Hudson, S. Nuttall, U. Krishnan, 2001, Molecular immunology.

Engineering of the Escherichia coli Im7 immunity protein as a loop display scaffold.

T. Mulhern, P. Hudson, S. Nuttall, 2006, Protein engineering, design & selection : PEDS.

Fragment Screening for the Modelling Community: SPR, ITC, and Crystallography

Thomas S. Peat, Olan Dolezal, Janet Newman, 2013 .

Selection and affinity maturation of IgNAR variable domains targeting Plasmodium falciparum AMA1

M. Foley, R. Anders, P. Hudson, 2004, Proteins.

Dimerisation strategies for shark IgNAR single domain antibody fragments.

V. Streltsov, S. Nuttall, U. Krishnan, 2006, Journal of immunological methods.

Engineered antibody intervention strategies for Alzheimer's disease and related dementias by targeting amyloid and toxic oligomers.

C. Masters, R. Cappai, P. Hudson, 2008, Protein engineering, design & selection : PEDS.

Central amyloid-β-specific single chain variable fragment ameliorates Aβ aggregation and neurotoxicity.

S. Nuttall, J. Nigro, K. Breheney, 2013, Protein engineering, design & selection : PEDS.

Preparation and biological evaluation of self-assembled cubic phases for the polyvalent inhibition of cholera toxin

P. Hartley, O. Dolezal, F. Separovic, 2011 .

Crystal structures of human ENPP1 in apo and bound forms

J. Newman, T. Peat, O. Dolezal, 2020, Acta crystallographica. Section D, Structural biology.

Inactivation and clearance of viruses during the manufacture of high purity factor IX.

D. Anderson, M. Hattarki, N. Goss, 2000, Biologicals : journal of the International Association of Biological Standardization.

Chromatographic removal and heat inactivation of hepatitis B virus during the manufacture of human albumin

D. Anderson, M. Hattarki, W. Adcock, 1998, Biotechnology and applied biochemistry.

Chromatographic removal and heat inactivation of hepatitis A virus during manufacture of human albumin

D. Anderson, M. Hattarki, Davida . Anderson, 1998, Biotechnology and applied biochemistry.

Kinetic Characterization of a Panel of High-Affinity Monoclonal Antibodies Targeting Ricin and Recombinant Re-Formatting for Biosensor Applications

O. Dolezal, C. Dogovski, S. Nuttall, 2014 .

Isolation and characterization of an IgNAR variable domain specific for the human mitochondrial translocase receptor Tom70.

P. Hudson, M. Ryan, S. Nuttall, 2003, European journal of biochemistry.

Cytotoxic properties of immunoconjugates containing melittin-like peptide 101 against prostate cancer: in vitro and in vivo studies

J. Werkmeister, K. Ow, P. Russell, 2004, Cancer Immunology, Immunotherapy.

Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth

Nghi Nguyen, Thomas S. Peat, Olan Dolezal, 2018, Nature.

An Efficient High-Throughput Screening Method for MYST Family Acetyltransferases, a New Class of Epigenetic Drug Targets

George Nikolakopoulos, Olan Dolezal, Thomas S Peat, 2011, Journal of biomolecular screening.

Construction, expression and characterisation of a single-chain diabody derived from a humanised anti-Lewis Y cancer targeting antibody using a heat-inducible bacterial secretion vector

Andrew M. Scott, Alexander A. Kortt, Barbara E. Power, 2001, Cancer Immunology, Immunotherapy.

Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth

A. Strasser, G. Smyth, J. Baell, 2018, Nature.

Single-chain Fv multimers of the anti-neuraminidase antibody NC10: the residue at position 15 in the V(L) domain of the scFv-0 (V(L)-V(H)) molecule is primarily responsible for formation of a tetramer-trimer equilibrium.

Olan Dolezal, Mark Walter, A. Kortt, 2003, Protein engineering.

Fragment Screening on Staphylococcus aureus HPPK – a Folate Pathway Target

T. Peat, O. Dolezal, J. Swarbrick, 2013 .

Structural studies of the tethered N‐terminus of the Alzheimer's disease amyloid‐β peptide

C. Masters, J. Varghese, O. Dolezal, 2013, Proteins.

Kinetic screening of antibody-Im7 conjugates by capture on a colicin E7 DNase domain using optical biosensors.

O. Dolezal, S. Nuttall, R. Hosse, 2009, Analytical biochemistry.

Exploring the Chemical Space around 8-Mercaptoguanine as a Route to New Inhibitors of the Folate Biosynthesis Enzyme HPPK

J. Newman, T. Peat, O. Dolezal, 2013, PloS one.

Fragment screening for a protein-protein interaction inhibitor to WDR5

J. Newman, T. Peat, O. Dolezal, 2019, Structural dynamics.

Structure-based design and development of functionalized Mercaptoguanine derivatives as inhibitors of the folate biosynthesis pathway enzyme 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase from Staphylococcus aureus.

J. Baell, Zhong-Chang Wang, J. Newman, 2014, Journal of medicinal chemistry.

Discovery of a highly potent, selective, orally bioavailable inhibitor of KAT6A/B histone acetyltransferases with efficacy against KAT6A-high ER+ breast cancer.

Chin Wee Tan, Dharmesh D. Bhuva, Eric C Greenwald, 2023, Cell chemical biology.

Biodistributions of intact monoclonal antibodies and fragments of BLCA-38, a new prostate cancer directed antibody

K. Ow, P. Russell, A. Kortt, 2004, Cancer Immunology, Immunotherapy.

Chromatographic removal and heat inactivation of hepatitis B virus during the manufacture of human albumin

M. Hattarki, Davida . Anderson, J. Davies, 1998, Biotechnology and applied biochemistry.

8-Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase.

J. Baell, Zhong-Chang Wang, T. Peat, 2018, Chemistry.