Recent advances in the development of novel protein scaffolds based therapeutics

被引:25
作者
Azhar, Asim [1 ]
Ahmad, Ejaj [1 ]
Zia, Qamar [1 ,2 ]
Rauf, Mohd. Ahmar [1 ]
Owais, Mohammad [1 ]
Ashraf, Ghulam Md [3 ]
机构
[1] Aligarh Muslim Univ, Interdisciplinary Biotechnol Unit, Aligarh, Uttar Pradesh, India
[2] Gagan Coll Management & Technol, Aligarh, Uttar Pradesh, India
[3] King Abdulaziz Univ, King Fahd Med Res Ctr, POB 80216, Jeddah 21589, Saudi Arabia
关键词
Immunoglobulin based protein scaffolds; Non-immunoglobulin based protein scaffolds; Adnectin; Anticalin; Aylmer; BiTE; DARPins; DART; Lipocalin; Knottin; TandAbs; CYSTINE-KNOT PEPTIDES; ALTERNATIVE BINDING-PROTEINS; CHAIN ANTIBODY CONSTRUCT; GROWTH-FACTOR RECEPTOR; AGOUTI-RELATED PROTEIN; ANKYRIN REPEAT; T-CELLS; BISPECIFIC ANTIBODIES; MOLECULAR RECOGNITION; ADNECTIN INHIBITOR;
D O I
10.1016/j.ijbiomac.2017.04.045
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
Antibodies occupy a central position when it comes to binding proteins with desired antigenic specificities. During the past decade, a plethora of recombinant or humanized versions of antibodies have entered clinical settings with outstanding accomplishments. Yet, they suffer from several drawbacks such as high molecular weight, limited tissue penetration, instability, high production cost, requirement for large doses and potential cytotoxicity. As a result, new generation of receptor proteins has been developed, that are derived from small and robust immunoglobulin (Ig) or non-immunoglobulin based "scaffolds". Combinatorial protein engineering has tremendous scope in the development of these protein scaffolds with immunoglobulin like specificity and/or prescribed binding functions. The advancement made in this regard can boast of developing various validated Ig based and non-Ig protein scaffolds with desirable therapeutic potential. The newly emerging"technology has profound scope in translational biology and offer matching replacement for existing immunotherapeutic agents. Only few data from early clinical studies are available yet, but many more are likely to come in the near future. Here, we provide a glimpse of recent clinical advances in the field of existing protein scaffolds. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:630 / 641
页数:12
相关论文
共 128 条
[1]   Cystine-knot peptides: emerging tools for cancer imaging and therapy [J].
Ackerman, Shelley E. ;
Currier, Nicolas V. ;
Bergen, Jamie M. ;
Cochran, Jennifer R. .
EXPERT REVIEW OF PROTEOMICS, 2014, 11 (05) :561-572
[2]   Anti-VEGFR2 and anti-IGF-1R-Adnectins inhibit Ewing's sarcoma A673-xenograft growth and normalize tumor vascular architecture [J].
Ackermann, Maximilian ;
Morse, Brent A. ;
Delventhal, Vera ;
Carvajal, Irvith M. ;
Konerding, Moritz A. .
ANGIOGENESIS, 2012, 15 (04) :685-695
[3]   Anticalins directed against the fibronectin extra domain B as diagnostic tracers for glioblastomas [J].
Albrecht, Valerie ;
Richter, Antonia ;
Pfeiffer, Sarah ;
Gebauer, Michaela ;
Lindner, Simon ;
Gieser, Eugenie ;
Schueller, Ulrich ;
Schichor, Christian ;
Gildehaus, Franz Josef ;
Bartenstein, Peter ;
Tonn, Joerg-Christian ;
Skerra, Arne ;
Glass, Rainer .
INTERNATIONAL JOURNAL OF CANCER, 2016, 138 (05) :1269-1280
[4]   Beyond Peptides and mAbs-Current Status and Future Perspectives for Biotherapeutics With Novel Constructs [J].
AlDeghaither, Dalal ;
Smaglo, Brandon G. ;
Weiner, Louis M. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 55 (03) :S4-S20
[5]   Therapeutic window of MuS110, a single-chain antibody construct bispecific for murine EpCAM and murine CD3 [J].
Amann, Maria ;
Brischwein, Klaus ;
Lutterbuese, Petra ;
Parr, Larissa ;
Petersen, Laetitia ;
Lorenczewski, Grit ;
Krinner, Eva ;
Bruckmeier, Sandra ;
Lippold, Sandra ;
Kischel, Roman ;
Lutterbuese, Ralf ;
Kufer, Peter ;
Baeuerle, Patrick A. ;
Schlereth, Bernd .
CANCER RESEARCH, 2008, 68 (01) :143-151
[6]   BiTE: a new class of antibodies that recruit T-cells [J].
Baeuerle, P. A. ;
Reinhardt, C. ;
Kufer, P. .
DRUGS OF THE FUTURE, 2008, 33 (02) :137-147
[7]  
Baeuerle PA, 2009, CURR OPIN MOL THER, V11, P22
[8]   Bispecific T-Cell Engaging Antibodies for Cancer Therapy [J].
Baeuerle, Patrick A. ;
Reinhardt, Carsten .
CANCER RESEARCH, 2009, 69 (12) :4941-4944
[9]   Tumor regression in cancer patients by very low doses of a T cell-engaging antibody [J].
Bargou, Ralf ;
Leo, Eugen ;
Zugmaier, Gerhard ;
Klinger, Matthias ;
Goebeler, Mariele ;
Knop, Stefan ;
Noppeney, Richard ;
Viardot, Andreas ;
Hess, Georg ;
Schuler, Martin ;
Einsele, Hermann ;
Brandl, Christian ;
Wolf, Andreas ;
Kirchinger, Petra ;
Klappers, Petra ;
Schmidt, Margit ;
Riethmueller, Gert ;
Reinhardt, Carsten ;
Baeuerle, Patrick A. ;
Kufer, Peter .
SCIENCE, 2008, 321 (5891) :974-977
[10]   High-throughput Sorting of an Anticalin Library via EspP-mediated Functional Display on the Escherichia coli Cell Surface [J].
Binder, Uli ;
Matschiner, Gabriele ;
Theobald, Ina ;
Skerra, Arne .
JOURNAL OF MOLECULAR BIOLOGY, 2010, 400 (04) :783-802