M
Matthew Hassink
Researcher at University of Delaware
Publications - 13
Citations - 497
Matthew Hassink is an academic researcher from University of Delaware. The author has contributed to research in topics: Bioconjugation & Tetrazine. The author has an hindex of 6, co-authored 10 publications receiving 450 citations. Previous affiliations of Matthew Hassink include National Institutes of Health.
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Journal ArticleDOI
Tetrazine-trans-cyclooctene ligation for the rapid construction of 18F labeled probes
Zibo Li,Hancheng Cai,Matthew Hassink,Melissa L. Blackman,Richard C. D. Brown,Peter S. Conti,Joseph M. Fox +6 more
TL;DR: A radiolabeling method for bioconjugation based on the Diels-Alder reaction between 3,6-diaryl-s-tetrazines and an (18)F-labeled trans-cyclooctene is described, making it an effective conjugation method within seconds at low micromolar concentrations.
Journal ArticleDOI
Development and Evaluation of 18F-TTCO-Cys40-Exendin-4: A PET Probe for Imaging Transplanted Islets
Zhanhong Wu,Shuanglong Liu,Matthew Hassink,Indu Nair,Ryan Park,Lin Li,Ivan Todorov,Joseph M. Fox,Zibo Li,John E. Shively,Peter S. Conti,Fouad Kandeel +11 more
TL;DR: 18F-TTCO-Cys40-exendin-4 demonstrated its great potential for transplanted islet imaging: the liver uptake value derived from small-animal PET images correlated well with the transplanted β-cell mass determined by immunostaining and the localizations of radioactive signal indeed corresponded to the distribution of islet grafts in the liver of is let-transplanted mice.
Journal ArticleDOI
Tetrazine-trans-cyclooctene ligation for the rapid construction of integrin αvβ₃ targeted PET tracer based on a cyclic RGD peptide.
Ramajeyam Selvaraj,Shuanglong Liu,Matthew Hassink,Chiun Wei Huang,Li Peng Yap,Ryan Park,Joseph M. Fox,Zibo Li,Peter S. Conti +8 more
TL;DR: The development of an extremely fast and efficient method for generating (18)F labeled probes based on the tetrazine-trans-cyclooctene ligation and the receptor specificity was confirmed by blocking experiments.
Journal ArticleDOI
Copper-Catalyzed Synthesis of 2,4-Disubstituted Allenoates from α-Diazoesters
TL;DR: A Cu-catalyzed method for coupling α-substituted-α-diazoesters with terminal alkynes to give substituted allenoates is described and a plausible mechanism is proposed, based in part on evidence against a mechanism that involves a Cu(I)-acetylide as a low-valent intermediate.
Journal ArticleDOI
Preclinical evaluation of a mercaptobenzamide and its prodrug for NCp7-targeted inhibition of human immunodeficiency virus.
Tracy L. Hartman,Lu Yang,A.N. Helfrick,Matthew Hassink,Nathaniel I. Shank,K. George Rosenker,Michael T. Scerba,Mrinmoy Saha,E. Hughes,A.Q. Wang,X. Xu,Pankaj Gupta,Robert W. Buckheit,Daniel H. Appella +13 more
TL;DR: Cell to cell transmission of HIV in multiple passages was significantly reduced in CEM-SS and human PBMCs by reducing progeny virus infectivity at compound concentrations greater than 2 μM, which is consistent with the proposed mechanism of action of the virus inactivating compounds.