Cellular IP₆ Levels Limit HIV Production while Viruses that Cannot Efficiently Package IP₆ Are Attenuated for Infection and Replication

Summary: HIV-1 hijacks host proteins to promote infection. Here we show that HIV is also dependent upon the host metabolite inositol hexakisphosphate (IP6) for viral production and primary cell replication. HIV-1 recruits IP6 into virions using two lysine rings in its immature hexamers. Mutation of either ring inhibits IP6 packaging and reduces viral production. Loss of IP6 also results in virions with highly unstable capsids, leading to a profound loss of reverse transcription and cell infection. Replacement of one ring with a hydrophobic isoleucine core restores viral production, but IP6 incorporation and infection remain impaired, consistent with an independent role for IP6 in stable capsid assembly. Genetic knockout of biosynthetic kinases IPMK and IPPK reveals that cellular IP6 availability limits the production of diverse lentiviruses, but in the absence of IP6, HIV-1 packages IP5 without loss of infectivity. Together, these data suggest that IP6 is a critical cofactor for HIV-1 replication

Effect of aerogel particle concentration on mechanical behavior of impregnated RTV 655 compound material for aerospace applications

Aerogels are a unique class of materials with superior thermal and mechanical properties particularly suitable for insulating and cryogenic storage applications. It is possible to overcome geometrical restrictions imposed by the rigidity of monolithic polyurea cross-linked silica aerogels by encapsulating micrometer-sized particles in a chemically resistant thermally insulating elastomeric sleeve. The ultimate limiting factor for the compound material\u27s performance is the effect of aerogel particles on the mechanical behavior of the compound material which needs to be fully characterized. The effect of size and concentration of aerogel microparticles on the tensile behavior of aerogel impregnated RTV655 samples was explored both at room temperature and at 77 K. Aerogel microparticles were created using a step-pulse pulverizing technique resulting in particle diameters between 425 m and 90 m and subsequently embedded in an RTV 655 elastomeric matrix. Aerogel particle concentrations of 25, 50, and 75 wt% were subjected to tensile tests and behavior of the compound material was investigated. Room temperature and cryogenic temperature studies revealed a compound material with rupture load values dependent on (1) microparticle size and (2) microparticle concentration. Results presented show how the stress elongation behavior depends on each parameter